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<rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6231">
    <dcterms:title><![CDATA[Integrating consumer perception in the selection of purple skin sweet potato cultivars]]></dcterms:title>
    <dcterms:subject><![CDATA[COMPORTAMIENTO DEL CONSUMIDOR
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    <dcterms:subject><![CDATA[EVALUACION SENSORIAL
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    <dcterms:subject><![CDATA[BATATAS
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    <dcterms:subject><![CDATA[MAPEO PROYECTIVO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[BACKGROUND: Sweet potato breeding programs need to integrate sensory characterization and hedonic perception in order to provide global markets with widely accepted products. The present work aimed at characterizing a series of purple skin<br />sweet potatoes differing in flesh coloration (from pale yellow to slight orange) from a sensory and physicochemical perspective. In addition, Uruguayan consumers' perception of the genotypes was explored. Special focus was placed on the influence of flesh color on consumers' expectations and hedonic perception of purple skin sweet<br />potatoes.<br />RESULTS: Sensory characterization based on projective mapping showed that the evaluated genotypes largely differed in their sensory characteristics, both in terms of flavour, texture and colour. Soluble solids and the concentration of individual sugars were not good predictors of sensory quality. In the appearance evaluation, consumers associated orange flesh with positive expected sensory characteristics and higher liking.<br />Flavour (sweetness and typical flavour) and texture (creaminess) were identified as key characteristics influencing consumers liking and description of sweet potato samples.<br />Among purple skin (&ldquo;criollo or boniato&rdquo; type) genotypes, INIA Cambar&aacute; was identified as the closest to the ideal sweet potato and described with the terms sweet, tasty, creamy and characteristic flavour.<br />CONCLUSION: Flesh colour was identified as a key driver of consumers' sensory and hedonic expectations. Results showed that Uruguayan consumers positively value traditional purple skin sweet potatoes with orange flesh, as it drives positive sensory expectations. However, after tasting, flesh colour does not seem to have a relevant influence on consumer liking.
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    <dcterms:creator><![CDATA[<strong>Lado, Joanna</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Esteban, Vicente</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Moltini, Ana In&eacute;s</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Alcaire, Florencia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ares, Gast&oacute;n</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Journal of the Science of Food and Agriculture, 2020. --p. 1-10, https://doi.org/10.1002/jsfa.10991
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    <dcterms:publisher><![CDATA[Wiley
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1002/jsfa.10991
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6230">
    <dcterms:title><![CDATA[<strong>The idealization of bottle-feeding: Content analysis of feeding bottles and teats packages in Uruguay</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[LECHE MATERNA
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    <dcterms:subject><![CDATA[LECHE MATERNA-SUSTITUTOS
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    <dcterms:subject><![CDATA[AMAMANTAMIENTO
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    <dcterms:subject><![CDATA[SALUD PUBLICA
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    <dcterms:subject><![CDATA[POLITICA ALIMENTARIA
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    <dcterms:subject><![CDATA[ETIQUETADO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Objective: The information displayed on the packages of feeding bottles and teats commercialized in Montevideo (Uruguay) was analyzed using content analysis with the goal of identifying key marketing practices that may discourage breastfeeding.<br />Design: The study was conducted as part of the periodic assessment performed by the Uruguayan government to monitor the marketing of breast-milk substitutes. All the feeding bottles and teats sold in 44 retail outlets selling breast-milk substitutes were purchased. The information available on the packages was analyzed using content analysis and descriptive statistics.<br />Setting: Montevideo, Uruguay.<br />Results: A total of 197 feeding bottles and 71 teats were found. The majority of the packages included information to enable caregivers to adequately use the products, including recommended age, instructions on how to use the products and instructions on the use of hygienic practices. However, the packages frequently included information that implied that bottle-feeding was equivalent to breastfeeding, particularly from a physiological perspective, or that idealized product use. Idealizations included ability to reduce colic, improvements in the feeding experience and improvements in children&rsquo;s health, wellbeing and development. Statements on the superiority of breastfeeding were infrequent.<br />Conclusions: Results from the present work showed the high prevalence of marketing practices on the packages of feeding bottles and teats that may discourage breastfeeding. Stricter and more detailed regulations seem necessary to enable caregivers to make informed feeding decisions for infants.
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    <dcterms:creator><![CDATA[<strong>Alcaire, Florencia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ant&uacute;nez, Luc&iacute;a</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>De Le&oacute;n, Carolina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Girona, Alejandra</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Rodr&iacute;guez, Raquel</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Gim&eacute;nez, Ana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Bove, Isabel</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ares, Gast&oacute;n</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Public Health Nutrition, 2020. --p. 1-9 DOI: 10.1017/S1368980020004176
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    <dcterms:publisher><![CDATA[Cambridge University Press
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[DOI: 10.1017/S1368980020004176
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6229">
    <dcterms:title><![CDATA[<strong>Ln(III)-Ni(II) heteropolynuclear metal organic frameworks of oxydiacetate with promising proton-conductive properties</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[TEORIA DE FUNCIONES DE LA DENSIDAD
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    <dcterms:subject><![CDATA[CONDUCTIVIDAD DE PROTONES
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    <dcterms:subject><![CDATA[ESTRUCTURA CRISTALINA
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    <dcterms:subject><![CDATA[OXIDIACETATO
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    <dcterms:subject><![CDATA[LANTANO
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    <dcterms:subject><![CDATA[NITROGENO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Heteropolynuclear metal organic frameworks (MOFs) of general formula [Ln2Ni3(oda)6(H2O)6]&middot;xH2O (oda = oxydiacetate, Ln = +3 rare earth ion) were synthesized and characterized. Most of them bear a honeycomb structure with 1D channels containing 11 to 14 crystallization water molecules per formula unit. The size of the channels and the number of crystallization water molecules they contain decrease as the Ln ionic radii gets smaller along the series from La to Tm. Besides, the water content changes reversibly with temperature and relative humidity conditions. Accordingly, the as-synthesized [Tm2Ni3(oda)6(H2O)6]&middot;11H2O picks-up water when exposed to 100% relative humidity atmosphere to become [Tm2Ni3(oda)6(H2O)6]&middot;14H2O. Computational calculations show the formation of a hydrogen bond network in which layers of water molecules are arranged and associated primarily to the polar groups of the framework walls, anticipating good proton conduction along the [001] channels. Furthermore, higher confinement of water molecules in the smaller channels could favor the water molecules mobility. Indeed, the protonic conductivity of [Tm2Ni3(oda)6(H2O)6]&middot;14H2O is 2.43 &times; 10&minus;3 S&middot;cm&minus;1 at 70 &deg;C, similar to standard conductive MOFbased materials reported. A vehicular carrier mechanism by means of H3O+ species diffusing along the 1D channels of the porous structure seems to be operative, with a high activation energy value of 1.46 eV.
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    <dcterms:creator><![CDATA[<strong>Igoa, Fernando</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Romero, Mariano</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Peinado, Guzm&aacute;n</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Castiglioni, Jorge</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Gonzalez Platas, Javier</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Faccio, Ricardo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Suescun, Leopoldo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kremer, Carlos</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Torres, Julia</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[CrystEngComm v.22, 2020. -- p. 5638-5648
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    <dcterms:publisher><![CDATA[Royal Society of Chemistry
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1039/D0CE00900H
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6228">
    <dcterms:title><![CDATA[<strong>Interactions and Dissociation Constants of Galactomannan Rendered Cellulose Films with Concavalin A by SPR Spectroscopy</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[CELULOSA
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    <dcterms:subject><![CDATA[GALACTOMANANO
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    <dcterms:subject><![CDATA[LECTINAS
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:subject><![CDATA[MONOSACARIDOS
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    <dcterms:abstract><![CDATA[Interactions of biomolecules at interfaces are important for a variety of physiological processes. Among these, interactions of lectins with monosaccharides have been investigated extensively in the past, while polysaccharide-lectin interactions have scarcely been investigated. Here, we explore the adsorption of galactomannans (GM) extracted from Prosopis anis on cellulose thin films determined by a combination of multi-parameter surface plasmon resonance spectroscopy (MP-SPR) and atomic force microscopy (AFM). The galactomannan adsorbs spontaneously on the cellulose surfaces forming monolayer type coverage (0.60  0.20 mgm
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    <dcterms:creator><![CDATA[<strong>Vilar&oacute;, Pilar</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Sampl, Carina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Teichert, Gundula</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Schlemmer, Werner</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Hobisch, Mathias</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Weissl, Michael</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Panizzolo, Luis</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ferreira, Fernando</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Spirk, Stefan</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Polymers v.12, 2020. -- p. 1-10.-- e3040
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    <dcterms:publisher><![CDATA[MDPI
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[doi:10.3390/polym12123040
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6227">
    <dcterms:title><![CDATA[<strong>A parallel segmented flow column interface for microflow HPLC-MS separations for environmental organic contaminant analyses</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[CONTAMINANTES ORGANICOS
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    <dcterms:subject><![CDATA[CROMATOGRAFIA LIQUIDA DE ALTA PRESION
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    <dcterms:subject><![CDATA[ESPECTROMETRIA DE MASAS
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    <dcterms:subject><![CDATA[ANALISIS DE TRAZAS
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    <dcterms:subject><![CDATA[TECNOLOGIA DE FLUJO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[<p>Interfacing a microflow velocity &lt; 100 &mu;L/min analyses between the separation technique and MS detection for environmental organic contaminant analyses have shown potential to decrease the matrix effect. However performing such volumetric flow rates typically involves the upgrade of equipment. A plug and play study to demonstrate the potential of the Parallel Segmented Flow (PSF) column technology without any changes to the separation or detection programmed settings can facilitate microflow separations on a HPLC 400 bar hyphenated MS system. Here, we present the PSF column that interfaced 54 &mu;L/min with electrospray tandem mass spectrometry (MS/MS) detection. Advantages of this alternative plug and play PSF microflow interfacing strategy include robust HPLC separation % RSD retention times &le; 0.38% and mobile phase consumption comparable to UHPLC consumption rates of 9 mL per analysis. The calculated matrix effect for microflow PSF was representative of reduced ion suppression/enhancement (&lt; &plusmn; 20%), with the exception of atrazine in river water which experienced medium suppression (&lt; &plusmn; 30%). The %ME is not yet competitive with capillary scale columns. The instrument detection limits (IDLs) calculated takes into account the variability (%RSD) and amount reaching the detector. The PSF had lower IDLs (3.09&ndash;7.66 pg) compared to the conventional column (1.53&ndash;31.61 pg), with the exception of atrazine&rsquo;s peak height calculation. This communication focused on the microflow PSF operation strictly on conventional HPLC tandem MS system, without hardware upgrades, and applicability for robust organic contaminant separations in environmental matrices (soil and river water).</p>
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    <dcterms:creator><![CDATA[<strong>Soliven, Arianne</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Pareja, Luc&iacute;a</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Shalliker, R. Andrew</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Heinzen, Horacio</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>P&eacute;rez Parada, Andr&eacute;s</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Microchemical Journal, 159, 2020.-- p. 1-8.-- e105444
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    <dcterms:publisher><![CDATA[Elsevier
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1016/j.microc.2020.105444
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6226">
    <dcterms:title><![CDATA[<strong>Identification of pyrazolotriazinones as potential agents for hyperuricemia treatment by using in vitro and in silico studies</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[HIPERURICEMIA
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    <dcterms:subject><![CDATA[ESTUDIOS IN VITRO
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    <dcterms:subject><![CDATA[ESTUDIOS IN SILICO
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    <dcterms:subject><![CDATA[PIRAZOLOTRIAZINONAS
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Heterocyclic compounds structurally related to purine bases have been described as anticonvulsants, antifungal, antiviral, anticancer, enzyme inhibitors, among others. In this work, pyrazolo[3,4-d][1-3]triazin-4-ones (2) and pyrazolo[4,3-d][1-3] triazin-4-ones (3) derivatives were evaluated as xanthine oxidase (XO) inhibitors. Compounds 3 showed the best activity with IC50 values range of 0.9&ndash;2.9 &mu;M. While the inhibition performance of pyrazolotriazinones was not more active than reference inhibitor allopurinol ( IC50 = 0.247 &plusmn; 0.004) &mu;M, these nuclei provide a platform for new and more potent XO inhibitors. Accordingly, molecular modeling methods were carried out to understand the compounds-enzyme binding mode. First, we have performed a qualitative SAR study using the MOE&trade; SAR tool. This study showed three common scaffolds and the most active was identified. These results are certainly valuable and will be taken into account in future synthesis of structurally related compounds. Furthermore, QSAR 2D and 3D studies were performed and structural requirements for the activity are reported. The obtained results led us to present the structural improvements for the rational design and synthesis of new pyrazolotriazinone derivatives with greater xanthine oxidase inhibitory activity than allopurinol.
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    <dcterms:creator><![CDATA[<strong>Sci&uacute;, M. Lourdes</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Santi, M. Daniela</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Cantero, Jorge</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Colomer, Juan P.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Paulino Zunini, Margot</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ortega, M. Gabriela</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Moyano, E. Laura</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[SN Applied Sciences v. 2, 2020. -- p. 1-14.--e1298
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    <dcterms:publisher><![CDATA[Springer Nature
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
<p>&nbsp;</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1007/s42452-020-2756-6
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6225">
    <dcterms:title><![CDATA[<strong>Identification of a Potential Zika Virus Inhibitor Targeting NS5 Methyltransferase Using Virtual Screening and Molecular Dynamics Simulations</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ENZIMAS
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    <dcterms:subject><![CDATA[ANTIVIRALES
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    <dcterms:subject><![CDATA[METILTRANSFERASA
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    <dcterms:subject><![CDATA[ZIKA-VIRUS
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[attractive molecular target for antivirals discovery against the Zika virus (ZIKV). Here, we report structure-based virtual screening of 42 390 structures from the Development Therapeutics Program (DTP) AIDS Antiviral Screen Database. Among the docked compounds, ZINC1652386 stood out due to its high affinity for MTase in comparison to the cocrystallized ligand MS2042, which interacts with the Asp146 residue in the MTase binding site by hydrogen bonding. Subsequent molecular dynamics simulations predicted that this compound forms a stable complex with MTase within 50 ns. Thus, ZINC1652386 may represent a promising ZIKV methyltransferase inhibitor.
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    <dcterms:creator><![CDATA[<strong>Santos, Felipe R. S.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Lima, William G.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Maia, Eduardo H. B.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Assis, Let&iacute;cia C.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Davyt, Danilo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Guterres Taranto, Alex</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ferreira, Jaqueline M. S.</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Journal of Chemical Information and Modeling v. 60, 2020.-- p. 562-568
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    <dcterms:publisher><![CDATA[American Chemical Society
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://dx.doi.org/10.1021/acs.jcim.9b00809
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6224">
    <dcterms:title><![CDATA[<strong>Unambiguous evaluation of chlorpyrifos and TCP bioremediation in laboratory and field experiments</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[INSECTICIDAS
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    <dcterms:subject><![CDATA[CLORPIRIFOS
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    <dcterms:subject><![CDATA[BIOTRANSFORMACION
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Chlorpyrifos is one of the most employed insecticides worldwide. It is moderately persistent in the environment. It degrades to 3, 5, 6- trichloro-2-pyridinol (TCP), the metabolite of toxicological concern to both human health and the environment. In the field, pesticides point contaminations occur during the operation of the application machinery. Biobeds made up of a biomixture containing straw, peat, and soil have been successfully developed to minimise these incidents. The retained pesticides are degraded by the microorganisms in the biomixture. Although the dissipation of chlorpyrifos in different biobeds has been studied, the fate of TCP received scarce attention. Biodegradation in specific bioreactors can only be assessed if it is evaluated through proper analytical methods. In this work chlorpyrifos and TCP dissipation in biobeds was studied with a previously fit for purpose analytical method. The lyophilised biomixture was extracted with ethyl acetate in an aqueous solution of NaCl and sodium tetraborate. The extract was cleaned up with alumina. Chlorpyrifos was determined by gas chromatography with electron capture and mass spectrometer detectors and TCP by liquid chromatography coupled to tandem mass spectrometry, using the negative Multiple Ion Mode. Recoveries of the two analytes, up to 2 mg kg&minus;1, were between 70% and 113% with RSDs below 16% and RSDwR below 19%. Further TCP confirmation was evaluated through Enhanced Product Ion mode for each ion. The dissipation of both analytes in laboratory biobeds inoculated with Abortiporus biennis using two different types of Uruguayan soils was assayed. Both bioreactors were able to dissipate the compounds after 60 days following different dissipation kinetics. Similar results were obtained after scaling up in a biobed under field conditions.
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    <dcterms:creator><![CDATA[<strong>Rivero, Anisleidy</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>G&eacute;rez, Natalia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Jes&uacute;s, Florencia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Niell, Silvina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Cerdeiras, Mar&iacute;a P&iacute;a</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Heinzen, Horacio</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Cesio, Mar&iacute;a Ver&oacute;nica</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[International Journal of Environmental Analytical Chemistry 2020.-- p. 1-14.--https://doi.org/10.1080/03067319.2020.1817429
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    <dcterms:publisher><![CDATA[Taylor and Francis
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1080/03067319.2020.1817429
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6223">
    <dcterms:title><![CDATA[<strong>Incorporation of Caprylic Acid into a Single Cell Oil Rich in Docosahexaenoic Acid for the Production of Specialty Lipids</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[LIPIDOS
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    <dcterms:subject><![CDATA[ACIDO DOCOSAHEXAENOICO
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    <dcterms:subject><![CDATA[ACIDO CAPRILICO
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    <dcterms:subject><![CDATA[ACIDOLISIS
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Research background. New sources of docosahexaenoic acid have recently been investigated aiming at infant formula fortification and dietary supplementation, among which the single cell oil with 40&ndash;50 % of this acid. Experimental approach. For this purpose, such an oil was blended with caprylic acid in amount substance ratio ranging from 1:1 to 5:1 and the blends were interesterified using either Novozym 435 or Lipozyme TL IM as the catalyst. The influence of the amount of excess free caprylic acid in the substrate, as well as the type of enzyme on the triacylglycerol rearrangement resulting from the synthesis of the structured lipids were evaluated. Results and conclusions. The regiospecific lipase Lipozyme TL IM seemed to induce transesterification among single cell oil triacylglycerols preferably by acidolysis with caprylic acid, which was directly proportional to the ratio of this acid in the substrate. In reactions catalyzed by the non-regiospecific lipase Novozym 435, a higher incorporation of caprylic acid into single cell oil triacylglycerols was observed than when using Lipozyme TL IM, independently of the oil/caprylic acid molar ratio. Novelty and scientific contribution. These results revealed the importance of combining the choice of the type of lipase, either regiospecific or not, with the amount ratios of free fatty acids and the substrate in acidolysis when aiming to produce structured lipids as a source of docosahexaenoic acid.
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    <dcterms:creator><![CDATA[<strong>Kanno Mathias, Daniela</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Piazentin Costa, Jacqueline</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Rodrigues Calvo, Carolina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Claro Da Silva, Roberta</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Converti, Attilio</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Segura, Nadia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Jachmani&aacute;n, Iv&aacute;n</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Gioielli, Luiz Antonio</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Rodriguez Ract, Juliana Neves</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Food Technology &amp; Biotechnology v. 58, no 4, 2020.-- p. 411-422
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    <dcterms:publisher><![CDATA[University of Zagreb, Faculty of Food Technology and Biotechnology
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.17113/ftb.58.04.20.6546
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6222">
    <dcterms:title><![CDATA[<strong>A Nitroalkene Benzoic Acid Derivative Targets Reactive Microglia and Prolongs Survival in an Inherited Model of ALS via NF-&kappa;B Inhibition</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ESCLEROSIS LATERAL AMIOTROFICA
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    <dcterms:subject><![CDATA[ACIDO NITROALQUENO BENZOICO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Motor neuron degeneration and neuroinflammation are the most striking pathological features of amyotrophic lateral sclerosis (ALS). ALS currently has no cure and approved drugs have only amodest clinically therapeutic effect in patients. Drugs targeting different deleterious inflammatory pathways in ALS appear as promising therapeutic alternatives. Here, we have assessed the potential therapeutic effect of an electrophilic nitroalkene benzoic acid derivative, (E)-4-(2-nitrovinyl) benzoic acid (BANA), to slow down paralysis progression when administered after overt disease onset in SOD1G93A rats. BANA exerted a significant inhibition of NF-&kappa;B activation in NF-&kappa;B reporter transgenicmice and microglial cell cultures. Systemic daily oral administration of BANA to SOD1G93A rats after paralysis onset significantly decreased microgliosis and astrocytosis, and significantly reduced the number of NF-&kappa;B-p65-positive microglial nuclei surrounding spinal motor neurons. Numerous microglia bearing nuclear NF-&kappa;B-p65 were observed in the surrounding of motor neurons in autopsy spinal cords from ALS patients but not in controls, suggesting ALS-associated microglia could be targeted by BANA. In addition, BANA-treated SOD1G93A rats after paralysis onset showed significantly ameliorated spinal motor neuron pathology as well as conserved neuromuscular junction innervation in the skeletal muscle, as compared to controls. Notably, BANA prolonged post-paralysis survival by ~30%, compared to vehicle-treated littermates. These data provide a rationale to therapeutically slow paralysis progression in ALS using small electrophilic compounds such as BANA, through a mechanism involving microglial NF-&kappa;B inhibition.
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    <dcterms:creator><![CDATA[<strong>Ibarburu, Sofia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kovacs, Mari&aacute;ngeles</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Varela, Valentina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Rodr&iacute;guez Duarte, Jorge</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ingold, Mariana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Invernizzi, Paulina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Porcal, Williams</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ar&eacute;valo, Ana Paula</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Perelmulter, Karen</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Bollati-Fogol&iacute;n, Mariela</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Escande, Carlos</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>L&oacute;pez, Gloria V.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>King, Peter</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Si, Ying</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kwon, Yuri</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Batthy&aacute;ny, Carlos</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Barbeito, Luis</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Trias, Emiliano</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Neurotherapeutics 2020.-- p. 1-17. https://doi.org/10.1007/s13311-020-00953-z
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    <dcterms:publisher><![CDATA[Springer
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1007/s13311-020-00953-z
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6221">
    <dcterms:title><![CDATA[<strong>In Vivo High Plasticity of Multi-Drug Resistant ST258 Klebsiella pneumoniae</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[KLEBSIELLA PNEUMONIAE
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    <dcterms:subject><![CDATA[BACTERIAS RESISTENTES
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Carbapenemase production in Enterobacterales clinical isolates is a global threat. Multi-drug resistant Klebsiella pneumoniae harboring carbapenemases are a major concern among the hospital settings in Latin America. Aim: The aim of this study was to analyze the genetic relatedness between three isolates of K. pneumoniae recovered from one patient in the same bacteriological round on the same day, which exhibited different susceptibility profiles to carbapenems (CP) and to colistin (Col). Isolates&rsquo; profiles were as follows (susceptible- S/resistant-R): CPS/ColR, CPR/ColR, and CPR/ColS. Pulse-field gel electrophoresis, multilocus sequence typing, and whole genome sequencing were performed. Conjugation assays were carried out and PCR determination in transconjugants (Tcs) was made for: blaCTX-M-groups, blaNDM, blaKPC, blaTEM, qnr alleles, aac(6&cent;)Ib-cr, ermB, and plasmid incompatibility groups (Inc). Results: All isolates belonged to the same clone, to ST258 and harbored blaCTX-M-14, blaCTX-M-15, qnrA1, qnrB1, aac(6&cent;)Ib-cr, and wzi154 (capsule-locus KL107). One isolate had additional wzi gene, wzi109 (capsulelocus KL36). In CPR isolates, the pattern was explained for blaNDM-1 or blaNDM-1/blaKPC-2 presence, and in ColR for IS5-like element insertion in mgrB at different positions. Co-mobilization of blaNDM-1/qnrA1 was associated to a different plasmid Inc (A/C-FII) in both blaNDM-1 donors. Mobilization of blaCTX-M-14 was related to IncI1 in one donor. Conclusion: These findings highlight the potential plasticity of ST258 K. pneumoniae clone. To the best of our knowledge, this is the first description of blaNDM-1/blaKPC-2-producing K. pneumoniae ST258 in Latin America.
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    <dcterms:creator><![CDATA[<strong>Garcia Fulgueiras, Virginia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Magallanes, Carmen</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Reyes, Victoria</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Cayota, Camila</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Galiana, Antonio</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Vieytes, Mariela</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Vignoli, Rafael</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>M&aacute;rquez, Carolina</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Microbial Drug Resistance 2020. -- p. 1-5.--e310
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    <dcterms:publisher><![CDATA[Mary Ann Liebert
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[DOI: 10.1089/mdr.2020.0310
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6220">
    <dcterms:title><![CDATA[In Vitro Bioaccessibility of Extractable Compounds from Tannat Grape Skin Possessing Health Promoting Properties with Potential to Reduce the Risk of Diabetes]]></dcterms:title>
    <dcterms:subject><![CDATA[ANTIINFLAMATORIOS
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    <dcterms:subject><![CDATA[ANTIOXIDANTES
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    <dcterms:subject><![CDATA[AMILASA
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    <dcterms:subject><![CDATA[DIABETES
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    <dcterms:subject><![CDATA[GLUCOSIDASA
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    <dcterms:subject><![CDATA[ENZIMAS
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    <dcterms:subject><![CDATA[UVA TANNAT
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    <dcterms:subject><![CDATA[TRANSPORTADORES DE GLUCOSA
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Diabetes pathogenesis encompasses oxidative stress, inflammation, insulin malfunctioning and partial or total insulin secretion impairment, which leads to a constant hyperglycemia. Polyphenols are known to possess bioactive properties, being Tannat grape skin a natural and sustainable source of these compounds. The present study aimed to find out the bioaccessibility of health-promoting molecules composing a multifunctional extract from Tannat grape skin obtained under hydro-alcoholic-acid conditions. The identification of phenolic compounds in the samples was performed by ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS). Subsequently, the samples were in vitro digested mimicking the human oral gastrointestinal conditions and the bioactivity of the digest (antioxidant, anti-inflammatory and modulation of glucose metabolism) was assessed. Eect on glucose metabolism was estimated by measuring carbohydrases activity and the functionality of glucose transporters of small intestine cells in presence and absence of the digested extract. Flavonoids, phenolic acids and phenolic alcohols were the major phenol compounds detected in the extract. The bioaccessible compounds protected the intestinal cells and macrophages against the induced formation of reactive oxygen species (ROS) and nitric oxide (NO). In addition, glucose transporters were inhibited by the digested extract. In conclusion, the bioaccessible compounds of the extract, including phenols, modulated key biochemical events involved in the pathogenesis of diabetes such as oxidative stress, inflammation and glucose absorption. The extract was eective under prevention with co-administration conditions supporting its potential for either reducing the risk or treating this disease.
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    <dcterms:creator><![CDATA[<strong>Fern&aacute;ndez Fern&aacute;ndez, Adriana Maite</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Iriondo DeHond, Amaia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Nardin, Tiziana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Larcher, Roberto</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Dellacassa, Eduardo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Medrano Fern&aacute;ndez, Alejandra</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Del Castillo, Mar&iacute;a Dolores</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Foods v. 9, 2020. -- p. 1-14.--e1575
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    <dcterms:publisher><![CDATA[MDPI
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[doi:10.3390/foods9111575
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6219">
    <dcterms:title><![CDATA[<strong>Associations of dietary intakes and serum levels of folate and vitamin B-12 with methylation of inorganic arsenic in Uruguayan children: Comparison of findings and implications for future research</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[VITAMINAS
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    <dcterms:subject><![CDATA[VITAMINA B12
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    <dcterms:subject><![CDATA[ARSENICO INORGANICO
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    <dcterms:subject><![CDATA[METILACION
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    <dcterms:subject><![CDATA[NI&Ntilde;OS
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    <dcterms:subject><![CDATA[URUGUAY
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Background: In the human body, inorganic arsenic (iAs) is methylated via the one-carbon cycle to form monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA). Lower proportions of iAs and MMA, and higher proportions of DMA in urine indicate efficient methylation; formation of DMA is thought to detoxify iAs and MMA. Studies on folate, vitamin B-12 and iAs methylation yield mixed findings, depending on whether folate and vitamin B-12 were assessed from diet, supplements, or using a blood biomarker. Objective: First, to compare the associations of serum concentrations and estimated intake of folate and vitamin B- 12 with indicators of iAs methylation. Second, to highlight the implications of these different B-vitamin assessment techniques on the emerging evidence of the impact of dietary modifications on iAs methylation. Methods: The study was conducted among ~7-year-old children from Montevideo, Uruguay. Serum folate and vitamin B-12 levels were measured on the Horiba ABX Pentra 400 analyzer; urinary arsenic was measured using High-Performance Liquid Chromatography on-line with Inductively Coupled Plasma Mass Spectrometry. Dietary intakes were assessed using the average of two 24-h dietary recalls. Linear regressions assessed the associations of serum levels, and dietary intakes of folate (n &frac14; 237) and vitamin B-12 (n &frac14; 217) with indicators of iAs methylation. Models were adjusted for age, sex, body mass index, total urinary arsenic, and rice intake. Results: Serum folate and vitamin B-12 levels were above the adequacy threshold for 99% of the participants. No associations were observed between serum folate, serum vitamin B-12, or vitamin B-12 intake and iAs methylation. Folate intake was inversely associated with urinary %MMA [&beta; (95% confidence interval):
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    <dcterms:creator><![CDATA[<strong>Desai, Gauri</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Millen, Amy E.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Vahter, Marie</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Queirolo, Elena I.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Peregalli, Fabiana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ma&ntilde;ay, Nelly</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Yu, Jihnhee</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Browne, Richard W.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kordas, Katarzyna</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Environmental Research v. 189,2020.--p. 1-6.--e109935
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    <dcterms:publisher><![CDATA[Elsevier
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:identifier><![CDATA[https://doi.org/10.1016/j.envres.2020.109935
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    <dcterms:coverage><![CDATA[Uruguay
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6218">
    <dcterms:title><![CDATA[<strong>Executive functions in school children from Montevideo, Uruguay and their associations with concurrent low-level arsenic exposure</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ARSENICO
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    <dcterms:subject><![CDATA[NI&Ntilde;OS
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    <dcterms:subject><![CDATA[VITAMINAS B
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    <dcterms:subject><![CDATA[URUGUAY
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Objective: Arsenic is a known childhood neurotoxicant, but its neurotoxicity at low exposure levels is still not well established. The aim of our cross-sectional study was to test the association between low-level arsenic exposure and executive functions (EF) among children in Montevideo. We also assessed effect modification by arsenic methylation capacity, a susceptibility factor for the health effects of arsenic, and by B-vitamin intake, which impacts arsenic methylation. Methods: Arsenic exposure was assessed as the specific gravity-adjusted sum of urinary arsenic metabolites (UAs) among 255 ~ 7 year-old children, and methylation capacity as the proportion of urinary monomethylarsonic acid (%MMA). Arsenic concentrations from kitchen water samples at participants&rsquo; homes were assessed. Bvitamin intake was calculated from the average of two 24-hour dietary recalls. EF was measured using three tests from the Cambridge Neuropsychological Test Automated Battery &ndash; Stockings of Cambridge (SOC), Intra-dimensional/ extra-dimensional shift task (IED), and Spatial Span (SSP). Generalized linear models assessed the association between U-As and EF measures; models were adjusted for age, sex, maternal education, possessions score, Home Observation for Measurement of the Environment Inventory score, season, and school clusters. Additional analyses were conducted to address issues of residual confounding and sample size. A &ldquo;B-vitamin index&rdquo; was calculated using principal component analysis. Effect modification by the index and urinary %MMA was assessed in strata split at the respective medians of these variables. Results: The median (range) U-As and water arsenic levels were 9.9 &mu;g/L (2.2, 47.7) and 0.45 &mu;g/L (0.1, 18.9) respectively, indicating that exposure originated mainly from other sources. U-As was inversely associated with the number of stages completed (&beta; = &minus;0.02; 95% CI: &minus;0.03, &minus;0.002) and pre-executive shift errors (&beta; = &minus;0.08; 95% CI: &minus;0.14, &minus;0.02) of the IED task, and span length of the SSP task (&beta; = &minus;0.01; 95% CI: &minus;0.02, &minus;0.004). There was no clear pattern of effect modification by B-vitamin intake or urinary %MMA. Conclusion: Low-level arsenic exposure may adversely affect executive function among children but additional, including longitudinal, studies are necessary to confirm these findings.
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    <dcterms:creator><![CDATA[<strong>Desai, Gauri</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Barg, Gabriel</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Vahter, Marie</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Queirolo, Elena I.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Peregalli, Fabiana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ma&ntilde;ay, Nelly</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Millen, Amy E.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Yu, Jihnhee</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kordas, Katarzyna</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Environment International v. 142 , 2020.-- p. 1- 9.--e 105883
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    <dcterms:publisher><![CDATA[Elsevier
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1016/j.envint.2020.105883
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    <dcterms:coverage><![CDATA[Uruguay
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6217">
    <dcterms:title><![CDATA[<strong>The First Use of a ReX5 Synthon to Modulate FeIII Spin Crossover via Supramolecular Halogen&middot;&middot;&middot;Halogen Interactions.</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[QUIMICA SUPRAMOLECULAR
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    <dcterms:subject><![CDATA[INTERACCIONES HALOGENAS
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    <dcterms:subject><![CDATA[HALOGENOS
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    <dcterms:subject><![CDATA[OXIDO DE HIERRO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[We have added the {ReIVX5}@ (X=Br, Cl) synthon to a pocket-based ligand to provide supramolecular design using halogen&middot;&middot;&middot;halogen interactions within an FeIII system that has the potential to undergo spin crossover (SCO). By removing the solvent from the crystal lattice, we &ldquo;switch on&rdquo; halogen&middot;&middot;&middot;halogen interactions between neighboring molecules, providing a supramolecular cooperative pathway for SCO. Furthermore, changes to the halogen-based interaction allow us to modify the temperature and nature of the SCO event.
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    <dcterms:creator><![CDATA[<strong>Busch, Rebecca</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Carter, Anthony B.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Konidaris, Konstantis F.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>K&uuml;hne, Irina A.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Gonz&aacute;lez, Ricardo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Anson, Christopher E.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Powell, Annie K.</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Chemistry A European Journal v. 26, 2020. -- p. 11835-11840
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    <dcterms:publisher><![CDATA[Wiley-VCH GmbH
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1002/chem.202001668.
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6216">
    <dcterms:title><![CDATA[<strong>Production and antiproliferative effect of violacein, a purple pigment produced by an Antarctic bacterial isolate</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[BACTERIAS
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    <dcterms:subject><![CDATA[NEOPLASMA
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    <dcterms:subject><![CDATA[CUELLO UTERINO
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    <dcterms:subject><![CDATA[VIOLACEINA
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:subject><![CDATA[CISPLATINO
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    <dcterms:abstract><![CDATA[We studied the production and the potential use of a purple-pigment produced by an Antarctic bacterial isolate. This pigment was identified as violacein, a metabolite produced by many bacterial strains and reported that it has antiproliferative activity in many cell lines. We analyzed the effect of temperature and the composition of the growth medium on pigment production, achieving the highest yield at 20 &deg;C in Tryptic Soy Broth medium supplemented with 3.6 g/L glucose. We doubled the yield of the pigment production when the process was scaled up in a 5 L bioreactor (77 mg/L of crude pigment). The pigment was purified and identified by mass spectrometry (DI&ndash;EI&ndash;MS) and Nuclear Magnetic Resonance (NMR) spectroscopy as violacein. We performed survival assays that showed that the pure pigment has antiproliferative activity and sensitize HeLa cells (cervix cell carcinoma) to cisplatin. Besides, the pigment did not show genotoxic activity in HeLa cells as found performing micronucleus assays. These results suggest that this pigment may be used as anticancer or sensitizer to cisplatin drug in cervix cancer.
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    <dcterms:creator><![CDATA[<strong>Alem, Diego</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Marizcurrena, Juan Jos&eacute;</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Saravia, Ver&oacute;nica</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Davyt, Danilo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Mart&iacute;nez L&oacute;pez, Wilner</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Castro‑Sowinski, Susana</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[World Journal of Microbiology and Biotechnology v. 36, 2020.-- p. 1-11.--e120
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    <dcterms:publisher><![CDATA[Springer
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1007/s11274-020-02893-4
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6215">
    <dcterms:title><![CDATA[<strong>Hymenobacter artigasi sp. nov., isolated from air sampling in maritime Antarctica</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[BACTERIAS ]]></dcterms:subject>
    <dcterms:subject><![CDATA[BACTERIAS AEROTRANSPORTADAS
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    <dcterms:subject><![CDATA[COLONIZACION BACTERIANA
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    <dcterms:subject><![CDATA[HYMENOBACTER ARTIGASI
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[A rod-shaped and Gram-stain-negative bacterial strain, 1BT, was isolated from an air sample collected at King George Island, maritime Antarctica. Strain 1BT is strictly aerobic, psychrophilic, catalase-positive, oxidase-positive and non-motile. Growth of strain 1BT is observed at 0&ndash;20&thinsp;&deg;C (optimum, 10&thinsp;&deg;C), pH 6.0&ndash;8.0 (optimum, pH 8.0) and in the presence of 0&ndash;1.0% NaCl (optimum, 0.5 % NaCl). Phylogenetic analysis based on 16S rRNA gene sequences places strain 1BT within the genus Hymenobacter and shows the highest similarity to Hymenobacter antarcticus VUG-A42aaT (97.5 %). The predominant menaquinone of strain 1BT is MK-7 and the major fatty acids (&gt;10 %) comprise summed feature 3 (C16 : 1 &thinsp;&omega;7c and/or C16 : 1 &thinsp;&omega;6c; 32.5 %), iso-C15 : 0 (17.6 %) and anteiso C15 : 0 (12.3 %). The polar lipid profile consists of the major compounds phosphatidylethanolamine, phosphatidylserine, two unidentified aminolipids and one unidentified phospholipid. The DNA G+C content based on the draft genome sequence is 61.2&thinsp;mol%. Based on the data from the current polyphasic study, 1BT represents a novel species of the genus Hymenobacter , for which the name Hymenobacter artigasi sp. nov. is suggested. The type strain is 1BT (=CCM 8970T=CGMCC 1.16843T).
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    <dcterms:creator><![CDATA[<strong>Roldan, Diego M</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Menes, Rodolfo Javier</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kyrpides, Nikos</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Woyke, Tanja</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Shapiro, Nicole</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Whitman William B</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Kralova, Stanislava</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Sedlacek, Ivo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Busse Hans, Jurgen</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[International journal of systematic and evolutionary microbiology v. 70, no.9, 2020. -- p. 4935-4941
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    <dcterms:publisher><![CDATA[Microbiology Society
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1099/ijsem.0.004362
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6214">
    <dcterms:title><![CDATA[<strong>Potential Therapeutic Role of Carnitine and Acetylcarnitine in Neurological Disorders</strong>.
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    <dcterms:subject><![CDATA[CARNITINA
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    <dcterms:subject><![CDATA[ACETILCARNITINA
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    <dcterms:subject><![CDATA[ENFERMEDADES NEUROLOGICAS<br />
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:subject><![CDATA[AMONIACO
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    <dcterms:subject><![CDATA[ANCIANOS
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    <dcterms:abstract><![CDATA[<div id="enc-abstract" class="abstract-content selected">
<p><strong class="sub-title"> Background: </strong> Current therapy of neurological disorders has several limitations. Although a high number of drugs are clinically available, several subjects do not achieve full symptomatic remission. In recent years, there has been an increasing interest in the therapeutic potential of L-carnitine (LCAR) and acetyl-L-carnitine (ALCAR) because of the multiplicity of actions they exert in energy metabolism, as antioxidants, neuromodulators and neuroprotectors. They also show excellent safety and tolerability profile.</p>
<p><strong class="sub-title"> Objective: </strong> To assess the role of LCAR and ALCAR in neurological disorders.</p>
<p><strong class="sub-title"> Methods: </strong> A meticulous review of the literature was conducted in order to establish the linkage between LCAR and ALCAR and neurological diseases.</p>
<p><strong class="sub-title"> Results: </strong> LCAR and ALCAR mechanisms and effects were studied for Alzheimer's disease, depression, neuropathic pain, bipolar disorder, Parkinson's disease and epilepsy in the elderly. Both substances exert their actions mainly on primary metabolism, enhancing energy production, through &beta;-oxidation, and the ammonia elimination via urea cycle promotion. These systemic actions impact positively on the Central Nervous System state, as Ammonia and energy depletion seem to underlie most of the neurotoxic events, such as inflammation, oxidative stress, membrane degeneration, and neurotransmitters disbalances, present in neurological disorders, mainly in the elderly. The impact on bipolar disorder is controversial. LCAR absorption seems to be impaired in the elderly due to the decrease of active transportation; therefore, ALCAR seems to be the more effective option to administer.</p>
<p><strong class="sub-title"> Conclusion: </strong> ALCAR emerges as a simple, economical and safe adjuvant option in order to impair the progression of most neurological disorders.</p>
</div>
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    <dcterms:creator><![CDATA[<strong>Maldonado, Cecilia</strong>
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    <dcterms:creator><![CDATA[<strong>V&aacute;zquez, Marta</strong>
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    <dcterms:creator><![CDATA[<strong>Fagiolino, Pietro</strong>
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    <dcterms:source><![CDATA[Current Pharmaceutical Design, 26(12), pp. 1277-1285
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    <dcterms:publisher><![CDATA[Bentham Sciences<br />
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[10.2174/1381612826666200212114038
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6213">
    <dcterms:title><![CDATA[<strong>Should emoji replace emotion words in questionnaire-based food-related consumer research?</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ALIMENTOS
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    <dcterms:subject><![CDATA[BEBIDAS
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    <dcterms:subject><![CDATA[COMPORTAMIENTO DEL CONSUMIDOR
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    <dcterms:subject><![CDATA[INVESTIGACION DE EMOCIONES
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    <dcterms:subject><![CDATA[INVESTIGACION DEL PRODUCTO
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    <dcterms:subject><![CDATA[EMOJI
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Emotion word questionnaires remain dominant in food-related emotion research despite acknowledged limitations. Emoji questionnaires can overcome some of these limitations but are not yet regarded as a strong alternative to emotion word questionnaires. We believe they have the potential to earn this right and use this invited opinion piece to explain why. Following a brief introduction about emoji, advantages of emoji questionnaires are summarised: &ndash; enhanced ecological validity, familiarity and cross-culturally shared meanings. We then address concerns that hinder uptake of emoji questionnaires, including emoji meanings/interpretations, appropriateness for older consumers and ability to represent emotional arousal (activation to deactivation). Finally, we offer suggestions for how to accelerate the uptake of emoji questionnaires in sensory and consumer science, which include: i) more applied studies using emoji questionnaires, ii) establishing emoji meanings in the context of eating of drinking, iii) adopting open-ended question formats, iv) comparing emoji and emotion word questionnaires, and v) establishing guidelines for emoji questionnaires. An important spill-over benefit of research to develop emoji questionnaires is that it exposes the lack of similar research for emotion word questionnaires. We encourage colleagues in the field to engage in the task of conducting needed methodological research on emoji and emotion words alike.
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    <dcterms:creator><![CDATA[<strong>Jaeger, Sara R.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Vidal, Leticia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ares, Gast&oacute;n</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Food Quality and Preference 2020.-- p. 1-5.-- https://doi.org/10.1016/j.foodqual.2020.104121
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    <dcterms:publisher><![CDATA[Elsevier
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1016/j.foodqual.2020.104121
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6212">
    <dcterms:title><![CDATA[<strong>Comparison of the Glycolytic and Alcoholic Fermentation Pathways of Hanseniaspora vineae with Saccharomyces cerevisiae Wine Yeasts</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[FERMENTACION
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    <dcterms:subject><![CDATA[VINO
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    <dcterms:subject><![CDATA[LEVADURAS
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    <dcterms:subject><![CDATA[GLUCOLISIS
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    <dcterms:subject><![CDATA[PIRUVATO QUINASA
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:subject><![CDATA[HANSENIASPORA VINEAE
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    <dcterms:abstract><![CDATA[Hanseniaspora species can be isolated from grapes and grape musts, but after the initiation of spontaneous fermentation, they are displaced by Saccharomyces cerevisiae. Hanseniaspora vineae is particularly valuable since this species improves the flavour of wines and has an increased capacity to ferment relative to other apiculate yeasts. Genomic, transcriptomic, and metabolomic studies in H. vineae have enhanced our understanding of its potential utility within the wine industry. Here, we compared gene sequences of 12 glycolytic and fermentation pathway enzymes from five sequenced Hanseniaspora species and S. cerevisiae with the corresponding enzymes encoded within the two sequenced H. vineae genomes. Increased levels of protein similarity were observed for enzymes of H. vineae and S. cerevisiae, relative to the remaining Hanseniaspora species. Key dierences between H. vineae and H. uvarum pyruvate kinase enzymes might explain observed dierences in fermentative capacity. Further, the presence of eight putative alcohol dehydrogenases, invertase activity, and sulfite tolerance are distinctive characteristics of H. vineae, compared to other Hanseniaspora species. The definition of two clear technological groups within the Hanseniaspora genus is discussed within the slow and fast evolution concept framework previously discovered in these apiculate yeasts.
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    <dcterms:creator><![CDATA[<strong>Valera, Mar&iacute;a Jos&eacute;</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Boido, Eduardo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Dellacassa, Eduardo</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Carrau, Francisco</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Fermentation v. 6, 2020. --p. 1-17.-- e78
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    <dcterms:publisher><![CDATA[MDPI
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[doi:10.3390/fermentation6030078
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6211">
    <dcterms:title><![CDATA[<strong>How do appearance and fragrance influence expectations and conceptual associations of cosmetic products? An exploratory case study with liquid hand soap.</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[COSMETICOS
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    <dcterms:subject><![CDATA[COMPORTAMIENTO DEL CONSUMIDOR
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    <dcterms:subject><![CDATA[FRAGANCIAS
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    <dcterms:subject><![CDATA[JABON LIQUIDO
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2021
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    <dcterms:abstract><![CDATA[The visual appearance and olfactory cues of liquid soap can trigger powerful expectations and associations in consumers' mind, which largely influence purchase decisions and shape product experience. In this context, the aims of the present work were: (a) to study the effect of appearance (color and transparency) and fragrance on conceptual associations and expectations of liquid hand soap and (b) to evaluate if preference patterns moderate such effect. Eight samples of liquid hand soap were obtained following a full factorial design with three 2-level variables: fragrance (herbal vs. fruity), color (green vs. orange), and transparency (transparent vs. pearly). Samples were evaluated by 104 female participants, who rated their liking and used a check-all-that-apply question to describe the samples in terms of sensory characteristics, expected functional aspects of the product, and conceptual associations. Results showed that appearance and transparency did not influence consumer liking. However, fragrance had a significant effect on consumer liking, expectations and conceptual associations of liquid hand soap. The effect of fragrance on expectations and conceptual associations depended on consumer liking of the fragrance. In addition, pearly appearance did not influence liking but had a significant effect on consumer expectations regarding functional aspects of the liquid hand soap. Practical applications Consumers associated the fragrance they preferred with a higher cleansing ability and perceived skin improvement, as well as with more positive emotional and conceptual associations. Pearly appearance was positively associated with functional aspects of the soaps, such as cleansing and moisturizing effects.
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    <dcterms:creator><![CDATA[<strong>Parente, Emma</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ares, Gast&oacute;n</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Journal of Sensory Studies 2020.--p. 1-6.--e12637
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    <dcterms:publisher><![CDATA[Wiley-Blackwell
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1111/joss.12637
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6210">
    <dcterms:title><![CDATA[<strong>Ultrasound assisted extraction of bioactivecompounds in fresh and freeze-dried Vitis viniferacv Tannat grape pomace</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ENOLOGIA
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    <dcterms:subject><![CDATA[SOLVENTE LIQUIDO-EXTRACCION
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    <dcterms:subject><![CDATA[ANTIOXIDANTES
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    <dcterms:subject><![CDATA[ULTRASONIDO
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    <dcterms:subject><![CDATA[VINOS TANNAT
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[Tannat red wine residues present a unique polyphenolic composition. Revalorization ofthis residue depends on adequate extraction technologies to assure process sustainability.Influence of temperature (15&minus;60◦C), ultrasound (US) power (0&minus;100 W) and US applicationtime (5&minus;50 min) on Ultrasound Assisted Extraction (UAE) of fresh and freeze-dried Tan-nat grape pomace was evaluated. UAE was performed in a US bath, following extractionkinetics throughout 50 min by assessing: total polyphenol content (TPC), total monomericanthocyanins (TMAC) and total antioxidant capacity (AOC). Additionally, HPLC analysiswas performed to determine extracted compounds&rsquo; profile. Results showed UAE enhancedextraction in both fresh and freeze-dried pomace. In fresh pomace, UAE yielded extracts50% richer in TPC and TMAC on average when compared to conventional extractions, whilein freeze-dried pomace 180% increase in extraction was achieved. In fresh and freeze-driedpomace, US application allowed extraction of different compounds with respect to con-ventional extraction. This work shows that UAE has potential for Tannat grape pomacevalorization, yet UAE conditions should be carefully selected to favour desired extract com-position.
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    <dcterms:creator><![CDATA[<strong>Gonz&aacute;lez, Mariana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Barrios, Sof&iacute;a</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Budelli, Eliana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>P&eacute;rez, Nicol&aacute;s</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Lema, Patricia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Heinzen, Horacio</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Food and Bioproducts Processing v. 124 ,2020.-- p. 378&ndash;386
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    <dcterms:publisher><![CDATA[Elsevier
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1016/j.fbp.2020.09.012
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6209">
    <dcterms:title><![CDATA[<strong>Highly Sensitive Detection of Zika Virus Nonstructural Protein 1 in Serum Samples by a Two-Site Nanobody ELISA</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ZIKA-VIRUS
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    <dcterms:subject><![CDATA[INMUNOENSAYO ELISA
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    <dcterms:subject><![CDATA[NANOCUERPOS
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    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA
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    <dcterms:subject><![CDATA[2020
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    <dcterms:abstract><![CDATA[The Zika virus was introduced in Brazil in 2015 and, shortly after, spread all over the Americas. Nowadays, it remains present in more than 80 countries and represents a major threat due to some singularities among other flaviviruses. Due to its easy transmission, high percentage of silent cases, the severity of its associated complications, and the lack of prophylactic methods and eective treatments, it is essential to develop reliable and rapid diagnostic tests for early containment of the infection. Nonstructural protein 1 (NS1), a glycoprotein involved in all flavivirus infections, is secreted since the beginning of the infection into the blood stream and has proven to be a valuable biomarker for the early diagnosis of other flaviviral infections. Here, we describe the development of a highly sensitive nanobody ELISA for the detection of the NS1 protein in serum samples. Nanobodies were selected from a library generated from a llama immunized with Zika NS1 (ZVNS1) by a two-step high-throughput screening geared to identify the most sensitive and specific nanobody pairs. The assay was performed with a sub-ng/mL detection limit in the sera and showed excellent reproducibility and accuracy when validated with serum samples spiked with 0.80, 1.60, or 3.10 ng/mL of ZVNS1. Furthermore, the specificity of the developed ELISA was demonstrated using a panel of flavivirus&rsquo; NS1 proteins; this is of extreme relevance in countries endemic for more than one flavivirus. Considering that the nanobody sequences are provided, the assay can be reproduced in any laboratory at low cost, which may help to strengthen the diagnostic capacity of the disease even in low-resource countries.
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    <dcterms:creator><![CDATA[<strong>Delfin Riela, Triana</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Rossotti, Mart&iacute;n</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Alvez-Rosado, Romina</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Leizagoyen, Carmen</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Gonz&aacute;lez-Sapienza, Gualberto</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Biomolecules v. 10, 2020. -- p. 1-14.--e 1652
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    <dcterms:publisher><![CDATA[MDPI
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    <dcterms:date><![CDATA[2020
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    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:format><![CDATA[Pdf
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[doi:10.3390/biom10121652
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6208">
    <dcterms:title><![CDATA[<strong>Impact of Hanseniaspora Vineae in alcoholic fermentation and ageing on lees of high-quality white wine</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[VINOS]]></dcterms:subject>
    <dcterms:subject><![CDATA[FERMENTACION]]></dcterms:subject>
    <dcterms:subject><![CDATA[VINOS BLANCOS]]></dcterms:subject>
    <dcterms:subject><![CDATA[POLISACARIDOS]]></dcterms:subject>
    <dcterms:subject><![CDATA[HANSENIASPORA VINEAE]]></dcterms:subject>
    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA]]></dcterms:subject>
    <dcterms:subject><![CDATA[2020]]></dcterms:subject>
    <dcterms:abstract><![CDATA[Abstract: Hanseniaspora vineae is an apiculate yeast that plays a significant role at the beginning of fermentation, and it has been studied for its application in the improvement of the aromatic profile of commercial wines. This work evaluates the use of H. vineae in alcoholic fermentation compared to Saccharomyces cerevisiae and in ageing on the lees process (AOL) compared to Saccharomyces and non-Saccharomyces yeasts. The results indicated that there were not significant dierences in basic oenological parameters. H. vineae completed the fermentation until 11.9% v/v of ethanol and with a residual sugars content of less than 2 g/L. Dierent aroma profiles were obtained in the wines, with esters concentration around 90 mg/L in H. vineae wines. Regarding the AOL assay, the hydroalcoholic solutions aged with H. vineae lees showed significantly higher absorbance values at 260 (nucleic acids) and 280 nm (proteins) compared to the other strains. However, non-significant dierences were found in the polysaccharide content at the end of the ageing process were found compared to the other yeast species, with the exception of Schizosaccharomyces pombe that released around 23.5 mg/L of polysaccharides in hydroalcoholic solution. The use of H. vineae by the wineries may be a viable method in fermentation and AOL to improve the quality of white wines.
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    <dcterms:creator><![CDATA[<strong>Del Fresno, Juan Manuel</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Escott, Carlos</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Loira, Iris</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Herbert-Pucheta, Jos&eacute; Enrique</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Schneider, R&eacute;mi</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Carrau, Francisco</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Cuerda, Rafael</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Morata, Antonio</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[Fermentation v.6, n&deg;3, 2020. -- pp. 1-14]]></dcterms:source>
    <dcterms:publisher><![CDATA[MDPI]]></dcterms:publisher>
    <dcterms:date><![CDATA[2020]]></dcterms:date>
    <dcterms:rights><![CDATA[<p><strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.</p>
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[Doi :10.3390/fermentation6030066
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</rdf:Description><rdf:Description rdf:about="https://riquim.fq.edu.uy/items/show/6207">
    <dcterms:title><![CDATA[<strong>Synthesis and solid-state characterization of diclofenac imidazolium monohydrate: an imidazolium pharmaceutical ionic liquid.</strong>]]></dcterms:title>
    <dcterms:subject><![CDATA[ANTIINFLAMATORIOS]]></dcterms:subject>
    <dcterms:subject><![CDATA[IMIDAZOLIO-SALES]]></dcterms:subject>
    <dcterms:subject><![CDATA[DICLOFENAC]]></dcterms:subject>
    <dcterms:subject><![CDATA[SINTESIS QUIMICA]]></dcterms:subject>
    <dcterms:subject><![CDATA[BIBLIOGRAFIA NACIONAL QUIMICA]]></dcterms:subject>
    <dcterms:subject><![CDATA[2020]]></dcterms:subject>
    <dcterms:abstract><![CDATA[A new imidazolium hydrated salt (DCF-IMI-H2O) of the nonsteroidal anti-inflammatory drug Diclofenac (DCF) was synthesized by solvent evaporation. This salt was fully characterized by X-ray diffraction (SCXRD, PXRD), infrared<br />spectroscopic (FT-IR) and thermal analysis (TGA, DSC, HSM) techniques. The salt formation is driven by deprotonation of the drug's carboxylic group, with proton transfer to the nitrogen atom of the imidazole ring. The water molecule plays an<br />important role in the 3D arrange observed in the crystal lattice, acting as a bridge between adjacent DCF and coformer molecules. The DCF-IMI-H2O exhibits an improved solubility profile when compared with the pure form of DCF, and similar<br />values when compared with sodium and potassium salts. This new salt proved stable under 75% relative humidity for one week and is stable after six-months storage at room conditions. The study of its thermal stability showed that a dehydration<br />process starts at around 45 &ordm;C, leading to the probably formation of an unstable anhydrous form, which melting around 92&deg;C. Spectroscopic studies showed that most of the salt is ionized when in amorphous state (liquid). These behaviors<br />features the new compound as an ionic liquid (IL), i.e., organic salt with melting point below 100 &ordm;C. Pharmaceutical ILs have been increasingly exploited in the past few years aiming improved properties regarding drug solubility, formulation and delivery (topical, transdermal and oral).
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    <dcterms:creator><![CDATA[<strong>da Silva, Cecilia P.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>&nbsp;Dayo Owoyemi, Bolaji C.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Alvarenga-Jr., Benedito R.</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Alvarez, Natalia</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Ellena, Javier</strong>]]></dcterms:creator>
    <dcterms:creator><![CDATA[<strong>Carneiro, Renato L.</strong>]]></dcterms:creator>
    <dcterms:source><![CDATA[CrystEngComm v.22, 2020. -- p. 5345-5354]]></dcterms:source>
    <dcterms:publisher><![CDATA[Royal Society of Chemistry]]></dcterms:publisher>
    <dcterms:date><![CDATA[2020]]></dcterms:date>
    <dcterms:rights><![CDATA[<strong>Informaci&oacute;n sobre Derechos de Autor</strong> (Por favor lea este aviso antes de abrir los documentos u objetos)<strong> La legislaci&oacute;n uruguaya protege el derecho de autor </strong>sobre toda creaci&oacute;n literaria, cient&iacute;fica o art&iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&oacute;n a lo establecido por el derecho com&uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&oacute;n de las siguientes condiciones de uso: Este documento es &uacute;nicamente para usos privados enmarcados en actividades de investigaci&oacute;n y docencia. No se autoriza su reproducci&oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&oacute;n o cita de partes debe indicarse el nombre de la persona autora.
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    <dcterms:language><![CDATA[Ingl&eacute;s
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    <dcterms:type><![CDATA[Art&iacute;culo
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    <dcterms:identifier><![CDATA[https://doi.org/10.1039/D0CE00723D
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