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                <text>Pyrolysis techniques provide an interesting way of recycling plastic wastes (PW) by transforming them into liquid fuels with high calorific values. Catalysts are employed in PW pyrolysis in order to favor cracking reactions; in that regard, cheap and abundant natural resources are being investigated as potential catalyst precursors. This article explores the pyrolysis of low-density polyethylene (LDPE) in a semibatch reactor under a reduced pressure of 300 torr and temperatures in the range of 370 �C&amp;ndash;430 �C. Three different solid materials, an activated carbon (AC1), a commercial Fluid cracking catalyst (FCC) and an aluminum- pillared clay (Al-PILC), were tested as catalysts for the pyrolysis process. Thermogravimetric analyzes were previously performed to select the most catalytically active materials. AC1 displayed very low catalytic activity while FCC and Al-PILC displayed high activity and conversion to liquid products. Hydrocarbons ranging from C5 to C28 were identified in the liquid products as well as significant changes in their composition when FCC and Al-PILC catalyst were used. Differences in the catalytic activity of the 3 solid materials are ascribed mainly to differences in their acid properties&#13;
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho de autor &lt;/strong&gt;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;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&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
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                <text>Rice bran oil was subject to different oxidation period under controlled condition to mimic the composition of the oil used in frying at low, medium and high oxidation degrees. By the hydrotreatment of the produced samples in a batch reactor at 100 bar and 350 ◦C, using Pd/Al2O3 as catalyst, they were converted to hydrocarbons with an efficiency over 95.5 %, regardless their oxidation degree. The chain length distribution of the hydrocarbon indicated that oil conversion took place preferentially through hydrodecarboxylation or hydrodecarbonylation or both combined, instead hydrodeoxigenation. Although the increase in the oxidation degree of the starting oil did not show any significant effect on the hydrocarbon yield, an enhanced effect on cracking was verified, suggesting that oxidized fatty acid chains were more vulnerable to be fractionated. Although all the products showed distillation curves similar to gasoil and over 85.5 % distilled within the diesel range, they reached 95 % distillate above the recommended temperature of 360 ◦C. Thus, they must be previously fractionated to be used as diesel fuels. Results demonstrate the convenience of the performed process for efficiently converting used cooking oils of different qualities to second-generation biogasoil.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt;&amp;nbsp;La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
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                <text>The oxidation of Met to methionine sulfoxide (MetSO) by oxidants such as hydrogen peroxide, hypochlorite, or peroxynitrite has profound effects on protein function. This modification can be reversed by methionine sulfoxide reductases (msr). In the context of pathogen infection, the reduction of oxidized proteins gains significance due to microbial oxidative damage generated by the immune system. For example, Mycobacterium tuberculosis (Mt) utilizes msrs (MtmsrA and MtmsrB) as part of the repair response to the host-induced oxidative stress. The absence of these enzymes makes Mycobacteria prone to increased susceptibility to cell death, pointing them out as potential therapeutic targets. This study provides a detailed characterization of the catalytic mechanism of MtmsrA using a comprehensive approach, including experimental techniques and theoretical methodologies. Confirming a ping-pong type enzymatic mechanism, we elucidate the catalytic parameters for sulfoxide and thioredoxin substrates (kcat/KM = 2656 &amp;plusmn; 525 M&amp;minus;1 s&amp;minus;1 and 1.7 &amp;plusmn; 0.8 &amp;times; 106 M&amp;minus;1 s&amp;minus;1, respectively). Notably, the entropic nature of the activation process thermodynamics, representing &amp;sim;85% of the activation free energy at room temperature, is underscored. Furthermore, the current study questions the plausibility of a sulfurane intermediate, which may be a transition-state-like structure, suggesting the involvement of a conserved histidine residue as an acid&amp;minus;base catalyst in the MetSO reduction mechanism. This mechanistic insight not only advances our understanding of Mt antioxidant enzymes but also holds implications for future drug discovery and biotechnological applications.</text>
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                <text>The reaction of [ReO2(PPh3)2I] with bis-diphenylphosphines (dpp) only produces complexes with general formula [ReO2(dpp)2]�. However, when the ligand used in this work (bis(diphenylphosphinomethane) (dppm)) reacts with the same precursor an interesting Re(I) complex is also afforded. By changing the reaction conditions, trans-[ReVO2(dppm)2]� and [ReI(dppm)3]I were obtained and characterized. The crystal structure of [Re(dppm)3]I&amp;middot;CH3OH&amp;middot;CH2Cl2 is given. In this compound, the P atoms are arranged in a strongly distorted octahedral coordination polyhedron around the rhenium center. This is the first case of a tris(dppm) complex ever reported</text>
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                <text>&lt;strong&gt;Rivero, M&lt;/strong&gt;</text>
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                <text>Polyhedron v. 19, no. 22-23, 2000. -- p. 2249-2254</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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                <text>&lt;strong&gt;Causas de la p&amp;eacute;rdida de mercurio en la destrucci&amp;oacute;n sulfon&amp;iacute;trica de la materia org&amp;aacute;nica: 1a. comunicaci&amp;oacute;n&lt;br /&gt;&lt;/strong&gt;</text>
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                <text>&lt;p dir="ltr"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p dir="ltr"&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p dir="ltr"&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho de autor&lt;/strong&gt;&amp;nbsp;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;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)&lt;/p&gt;&#13;
&lt;span id="docs-internal-guid-9d2103f7-7fff-c813-00c7-2528fd4891ff"&gt;&lt;strong&gt;ADVERTENCIA:&lt;/strong&gt;&amp;nbsp;La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/span&gt;</text>
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                <text>CdTe films were grown onto amorphous substrates by electron beam deposition (EB) and by horizontal and vertical physical vapor deposition (HPVD and VPVD). The films were characterized by X-ray diffraction, scanning electron microscopy (SEM) and by measuring their electrical resistivity and response to X-rays. A 4-Am-thick layer deposited by EB had uniform grain size, preferred growth orientation of (1 1 1). However, the films did not have any response to X-rays since the resistivity of the layer was only 104 V cm. The grain distribution, grain size and roughness of films grown by HPVD were nonuniform. VPVD gave uniform films 35 to 150 Am thick, grain size between 5 and 25 Am, preferred growth orientation of (1 1 1), resistivity of 106 V cm and linear response to X-rays. Correlations between texture and grain size with substrate temperature were established.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(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)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>&lt;p&gt;Problem&lt;br /&gt;Untreated celiac disease (CD) is often associated with early miscarriages,&amp;nbsp;infertility, and alterations in menstrual cycle. Tissue transglutaminase&amp;nbsp;(tTG) antibodies could be involved by interfering with tTG transamidating&amp;nbsp;activity and &amp;frasl; or biological functions mediated by its interaction with&amp;nbsp;fibronectin (FN).&lt;/p&gt;&#13;
&lt;p&gt;&lt;br /&gt;Method of study&lt;br /&gt;The correlation between the presence of extra-digestive disorders and&amp;nbsp;the reactivity of sera against tTG-FN and its effects on tTG transamidating&amp;nbsp;activity was analyzed in a group or 50 women with recently diagnosed&amp;nbsp;CD.&lt;/p&gt;&#13;
&lt;p&gt;&lt;br /&gt;Results&lt;br /&gt;Heterogeneous behavior was observed among serum samples derived&amp;nbsp;from patients with different complaints, suggesting that differences in&amp;nbsp;fine specificity patterns could condition clinical outcome. Sera from&amp;nbsp;women with gynecological and &amp;frasl; or obstetric problems induced significant&lt;br /&gt;inhibition of in vitro enzymatic activity in comparison with those without&amp;nbsp;these kinds of disorders.&lt;/p&gt;&#13;
&lt;p&gt;&lt;br /&gt;Conclusions&lt;br /&gt;The significant correlation observed between serum effects and clinical&amp;nbsp;profile suggests a putative involvement of tTG-specific antibodies in&amp;nbsp;gynecological and &amp;frasl; or obstetric disorders during active CD.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Mu&amp;ntilde;oz, Federico&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Acosta, Gis&amp;eacute;le&lt;/strong&gt;</text>
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                <text>American Journal of Reproductive Immunology v. 66, no. 6, 2011. -- p. 476-481</text>
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            <description>An entity responsible for making the resource available</description>
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                <text>John Wiley &amp;amp; Sons A/S</text>
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            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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                <text>&lt;p align="LEFT"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(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)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>The inositol pyrophosphate messengers (PP-InsPs) are emerging as an important class of cellular regulators. These molecules have been linked to numerous biological processes, including insulin secretion and cancer cell migration, but how they trigger such a wide range of cellular responses has remained unanswered in many cases. Here, we show that the PP-InsPs exhibit complex speciation behaviour and propose that a unique conformational switching mechanism could contribute to their multifunctional effects. We synthesised non-hydrolysable bisphosphonate analogues and crystallised the analogues in complex with mammalian PPIP5K2 kinase. Subsequently, the bisphosphonate analogues were used to investigate the protonation sequence, metal-coordination properties, and conformation in solution. Remarkably, the presence of potassium and magnesium ions enabled the analogues to adopt two different conformations near physiological pH. Understanding how the intrinsic chemical properties of the PP-InsPs can contribute to their complex signalling outputs will be essential to elucidate their regulatory functions.</text>
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&lt;p&gt;&lt;strong&gt; ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>We studied Abcc mediated-transport in middle and posterior intestine of the rainbow trout, Oncorhynchus mykiss. Luminal and serosal transport were evaluated in everted and non-everted intestinal sacs, respectively, incubated with 1-chloro-2,4-dinitrobenzene (CDNB; 200 &amp;mu;M). CDNB enters the cells and is conjugated with glutathione via glutathione S-transferase (GST) to form 2,4-dinitrophenyl-S-glutathione (DNP-SG), a known Abcc substrate. DNP-SG concentration in the bath was recorded every 10 min, in order to calculate the mass-specific transport rate. For evaluating the possible involvement of Abcc proteins in microcystin-LR (MCLR) transport, 1.135 &amp;mu;M MCLR was added to the bath or inside the sacs, in everted or non-everted preparations, respectively. Both luminal and serosal DNP-SG efflux were significantly inhibited by MCLR. A concentration-response curve obtained using strips from middle intestine yielded an IC50 value of 1.33 &amp;mu;M MCLR. The Abcc inhibitor, MK571 produced concentration-dependent inhibition of DNP-SG similar to that produced by MCLR. Since competition of MCLR and CDNB as GST substrates could bias the DNP-SG transport results, we evaluated the effects of MCLR on calcein efflux, which does not depend on GST activity. We applied the non-fluorescent, cell-permeant compound calcein-AM (0.25 &amp;mu;M) to middle intestinal strips and recorded the efflux of its hydrolysis product, the fluorescent Abcc substrate calcein. 2.27 &amp;mu;M MCLR and 3 &amp;mu;M MK571 inhibited calcein efflux (17.39 and 20.2%, respectively). Finally, MCLR interaction with Abcc transporters was evaluated by measuring its toxic intracellular effects. Middle intestinal segments were incubated in saline solution with 1.135 &amp;mu;M MCLR (MC1), 2.27 &amp;mu;M MCLR (MC2), 3 &amp;mu;M MK571 (MK) or 1.135 &amp;mu;M MCLR+3 &amp;mu;M MK571 (MC1/MK). After 1h, GSH concentration, protein phosphatase 1 and 2A (PP1, PP2A) and GST activities were measured in each segment. MC1did not produce significant effect while MC1/MK and MC2 significantly inhibited PP1and PP2A in similar proportions (34-49%). MK alone significantly increased PP2A activity (40%) with no effect in any other variable. GST activity and GSH concentration were not affected by any treatment. Concentration-response curves for MCLR (1.135 to 13.62 &amp;mu;M) alone or plus 3 or 6 &amp;mu;M MK571 were obtained using PP1 activity as response variable. The IC50 values were 1.0, 0.52, and 0.37 &amp;mu;M, respectively. Our results suggest that O. mykiss enterocytes are capable of eliminating MCLR by GST-mediated conjugation and luminal excretion through an Abcc-like apical transporter. This mechanism would prevent toxic effects and reduce the toxin uptake into the blood, which is likely mediated by basolateral Abccs.</text>
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                <text>&lt;p align="LEFT"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(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)&lt;/p&gt;&#13;
&lt;p style="margin-bottom: 0cm;"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
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                <text>&lt;strong&gt;Celulasas sicr&amp;oacute;filas, una innovaci&amp;oacute;n en la industria del bioetanol&lt;/strong&gt;</text>
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                <text>En este trabajo de tesis se han explorado dos metodolog&amp;iacute;as en la b&amp;uacute;squeda de la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. Estas metodolog&amp;iacute;as fueron planteadas para lograr sintetizar fases de boratos de zinc en distintos rangos de temperaturas, lo que brinda grandes posibilidades en el desarrollo de aplicaciones tecnol&amp;oacute;gicas. Empleando la s&amp;iacute;ntesis por combusti&amp;oacute;n de gel asistida se pretendi&amp;oacute; sintetizar boratos de zinc a temperatura mayores a 250 &amp;deg;C, para los cuales se esperaba obtener nanopart&amp;iacute;culas que fueran importantes en el desarrollo de nuevos aditivos de materiales que se preparan a altas temperaturas, por ejemplo, pl&amp;aacute;sticos. A partir de las s&amp;iacute;ntesis asistidas por micelas reversas, se pretendi&amp;oacute; obtener boratos de zinc a baja temperatura, por ejemplo, los aminoboratos de zinc [Zn(NH3)3B4O5(OH)4]&amp;middot;H2O (ZB1) y Zn3(H2B3O7)2&amp;middot;2NH3&amp;middot;4H2O (ZB2), reportados previamente durante mi trabajo de Licenciatura en Qu&amp;iacute;mica. Mediante la metodolog&amp;iacute;a de combusti&amp;oacute;n de gel asistida se logr&amp;oacute; sintetizar la fase ZnB4O7. Los resultados presentados para estas s&amp;iacute;ntesis son contundentes respecto a los procesos qu&amp;iacute;micos que tienen lugar en el sistema estudiado. El medio reductor ofrecido por la alta concentraci&amp;oacute;n de amonio da lugar a la formaci&amp;oacute;n de carbono amorfo que permanece como principal impureza en las muestras obtenidas, no siendo posible la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. La obtenci&amp;oacute;n de ZB2 por m&amp;eacute;todos de baja temperatura fue posible a partir de un sistema coloidal mantenido por agitaci&amp;oacute;n formado por agua, CTAB, hexano y diferentes alcoholes como cosurfactantes. Para estos sistemas se obtuvo la fase cristalina ZB2 con tama&amp;ntilde;os entre 100 y 1000 nm, report&amp;aacute;ndose tama&amp;ntilde;os menores a 150 nm cuando se emple&amp;oacute; isopropanol como cosurfactante. Tambi&amp;eacute;n se sintetiz&amp;oacute; la fase ZB2 en un medio de micelas reversas. Este &amp;uacute;ltimo es uno de los logros m&amp;aacute;s importantes de este trabajo, ya que se consigui&amp;oacute; estabilizar un sistema de micelas reversas y obtener un producto con un tama&amp;ntilde;o de part&amp;iacute;cula menor a 150 nm. Este trabajo es un aporte importante en la qu&amp;iacute;mica b&amp;aacute;sica de estos sistemas, abriendo puertas a futuros estudios de s&amp;iacute;ntesis en sistemas de micelas reversas. La metodolog&amp;iacute;a utilizada para determinar las condiciones de formaci&amp;oacute;n de micelas reversas es extrapolable a cualquier sistema de obtenci&amp;oacute;n de compuestos qu&amp;iacute;micos a partir de una soluci&amp;oacute;n acuosa con par&amp;aacute;metros de concentraci&amp;oacute;n y fuera i&amp;oacute;nica adecuados. Los estudios microbiol&amp;oacute;gicos realizados sobre la fase ZB2 permitieron confirmar la actividad antif&amp;uacute;ngica y antibacteriana presentada por este compuesto y su dependencia con el tama&amp;ntilde;o de part&amp;iacute;cula</text>
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                <text>&lt;strong&gt;Herrera, Lorena.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=729d3d9bb07d7be0ba5e4dc762c01e29" target="_self"&gt;Franco Fraguas, Laura&lt;/a&gt;&lt;/strong&gt;</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Administraci&amp;oacute;n Nacional de Combustibles, Alcohol y Portland (Uruguay)</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;br /&gt; &lt;br /&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;br /&gt; &lt;br /&gt; (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)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Espa&amp;ntilde;ol</text>
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                <text>Uruguay</text>
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        <name>Cemento Portland</name>
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        <name>Lavalleja (Uruguay)</name>
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                  <text>Bibliografía Nacional Química</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                  <text>Departamento de Documentación y Biblioteca</text>
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                  <text>RIQUIM</text>
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            <name>Title</name>
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                <text>&lt;strong&gt;Centellograf&amp;iacute;a en el Desarrollo Farmac&amp;eacute;utico : estudios In Vitro e In Vivo de Comprimidos de Ranitidina&lt;/strong&gt;</text>
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                <text>RADIOFARMACIA</text>
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                <text>RANITIDINA</text>
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                <text>CENTELLOGRAFIA</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>2000</text>
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                <text>El presente trabajo tiene como objetivo evaluar la utilidad de los estudios centellogra&amp;iacute;ficos in viao e in vivo en el desarrob de una formulaci&amp;oacute;n farmac&amp;eacute;utica. Se eligi&amp;oacute; como trazador del proceso el radiofa&amp;iacute;rmaco 99mTc-a&amp;iacute;cido dietilentriaminopentaac&amp;eacute;tico, que se incorpor&amp;oacute; a 4 formulaciones (Fi a F4) de comprimidos de ranitidina. Se llevaron a cabo estudios de estabilidad del radiofa&amp;iacute;rmaco en polvos, granulados y comprimidos. Las formulaciones en las cuales se verific&amp;oacute; su estabilidad durante 24 h (F2 y F4) fueron utilizadas para ensayos in v i h de disoluci&amp;oacute;n y desintegraci&amp;oacute;n y estudios en 6 voluntarios sanos. La desintegraci&amp;oacute;n in vibo e in vivo fue monitoreada por centellogra&amp;ntilde;a gamma. El radiof4rmaco present&amp;oacute; diferentes cin&amp;eacute;ticas de disoluci&amp;oacute;n a partir de F2 y P4, siendo las respectivas constantes del mismo orden que para la ranitidina en cada formulaci&amp;oacute;n en estudio. La centellograf&amp;iacute;a posibilit&amp;oacute; establecer una correlaci&amp;oacute;n entre las constantes de desintegraci&amp;oacute;n in v i h e in vivo. Esto permitirla predecir el comportamiento en el tracto gastro-intestinal de cada formulaci&amp;oacute;n a partir de la desintegraci&amp;oacute;n in viao. Los estudias centellogra&amp;iacute;-' ricos brindan informaci&amp;oacute;n relevante con economla de tiempo en etapas de desarrollo. SUMMARY."Scintigraphy in Pharmaceutical Development Stage / In vitro 1 In vivo Studies of Ranitidine Tablets". Scintigraphic studies in vitro and in vivo were carried out to evaluate their utility in the development of pharmaceutical forms. A radiopharmaceutical (99mTc-dietilentr&amp;iacute;aminepentacetic acid) was incorporated as the tracer in four tablet formulations (Fi to F4) of ranitidine. Stability of the radiopharmaceuticai with the excipients, granulates and tablets was assesed. Those formulations where the tracer verified stability during 24 hours (F2 and F4) were tested through dissolution and desintegration studies. Scintigraphic images were acquired in gamma camera after administration of ranitidine tablets to 6 healthy volunteers. The radiopharmaceutical showed different dissolution profiles from F2 and F4, The dissolution constants for ranitidine and the radiopharmaceutical had similar vaiues in each formulation. A correlation between in vitrolin vivo disintegration was established. This would enable to predict gastro-intestinal transit ftom in vitro disintegration data. Scintigraphjc studies give relevant information in short time dunng development stages of a pharmaceutical dosage.</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=5d09a7215277d361b69aefbb081c9fa8"&gt;&lt;strong&gt;Ter&amp;aacute;n, Mariella&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Paolino, Andrea&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=1023bf078c82efde0baa86eb3a1163e6"&gt;&lt;strong&gt;Savio, Eduardo&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Gaudiano, Javier&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Le&amp;oacute;n, Alba&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Frier, Malcolm&lt;/strong&gt;</text>
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                <text>Acta Farmace&amp;uacute;tica Bonaerense v. 19, no. 3, 2000. -- p. 217-224</text>
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            <name>Publisher</name>
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                <text>Colegio de Farmac&amp;eacute;uticos de la Provincia de Buenos Aires</text>
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            <name>Date</name>
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                <text>2000</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;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)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Espa&amp;ntilde;ol</text>
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                <text>ISSN: 0326-2383</text>
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        <name>Raditidina</name>
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