<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/">
<channel rdf:about="https://hdl.handle.net/10481/26258">
<title>APh, vol. 50(2)</title>
<link>https://hdl.handle.net/10481/26258</link>
<description/>
<items>
<rdf:Seq>
<rdf:li rdf:resource="https://hdl.handle.net/10481/27469"/>
<rdf:li rdf:resource="https://hdl.handle.net/10481/27468"/>
<rdf:li rdf:resource="https://hdl.handle.net/10481/27467"/>
<rdf:li rdf:resource="https://hdl.handle.net/10481/27466"/>
<rdf:li rdf:resource="https://hdl.handle.net/10481/27464"/>
</rdf:Seq>
</items>
<dc:date>2026-04-03T23:39:03Z</dc:date>
</channel>
<item rdf:about="https://hdl.handle.net/10481/27469">
<title>Hook effect in radioligand assay for Anti Glutamic Acid Decarboxylase (Anti-GAD65). Influence of temperature and physicochemical interpretation</title>
<link>https://hdl.handle.net/10481/27469</link>
<description>Hook effect in radioligand assay for Anti Glutamic Acid Decarboxylase (Anti-GAD65). Influence of temperature and physicochemical interpretation
Peris-Conejero, T.; Olivares-Pallerols, R.; García-Ruiz, H.; Moreno-Frigols, J.I.
Background: Radioligand assay is one of the principal methods used for analytical&#13;
determination of the Anti-GAD65 concentration. We studied the influence of temperature on&#13;
the calibration curves obtained by such a method&#13;
Matherial and Methods: We used a commercially available RIA kit for Anti-GAD65 and a&#13;
gamma counter. Data was analyzed using Statistica software.&#13;
Results and Discusion: Activities bound to the antibody increase with temperature. There&#13;
was a decrease in activity for high concentrations attributable to the "hook effect". We propose a simple physicochemical model that justifies satisfactorily the results.; Objetivo: El análisis por radioligando es uno de los métodos principales utilizados en la&#13;
determinación analítica del Anti-GAD65. Se ha estudiado la influencia de la temperatura&#13;
sobre las gráficas de calibración obtenidas por dicha técnica.&#13;
Material y Métodos: Usamos un kit comercial para Anti-GAD65 y un contador gamma. Los&#13;
resultados son analizados mediante el programa Statistica.&#13;
Resultados y Discusión: Las actividades ligadas al anticuerpo aumentan con la temperatura.&#13;
Se observa una disminución de la actividad para altas concentraciones atribuible al llamado “efecto anzuelo”. Se propone un sencillo modelo fisicoquímico que justifica&#13;
satisfactoriamente los resultados
</description>
</item>
<item rdf:about="https://hdl.handle.net/10481/27468">
<title>Development and validation of enzymatic method for the determination of alcohol in immunoglobulin and albumin</title>
<link>https://hdl.handle.net/10481/27468</link>
<description>Development and validation of enzymatic method for the determination of alcohol in immunoglobulin and albumin
Carrillo-Cabrera, D.; González-Farah, A.; Rodríguez-Bernal, J.; Suárez-Pérez, Y.; Fernández-Cervera, M.; Veliz Rivera, J.
Se desarrolló y validó un método enzimático para la cuantificación del contenido de alcohol en los IFAs de Inmunoglobulina y Albúmina. En ambos casos el procedimiento analítico&#13;
resultó lineal, exacto, preciso y específico para el control de calidad. Se demostró que el&#13;
método fue lineal en el rango de 6.0 a 19.0 mg de alcohol/g de proteína para la albúmina y de&#13;
9.2 a 27.6 mg de alcohol/g de proteína para la inmunoglobulina, respectivamente. El método sugerido se aplicó con éxito en la determinación del contenido de alcohol como impureza en lotes industriales.; An enzymatic method for the quantification of alcohol content in immunoglobulin and&#13;
albumin was developed and validated. In both materials, the analytical procedure was linear,&#13;
accurate, precise and specific. The method was linear in the range from 6.0 to 19.0 mg of&#13;
alcohol/g of protein to albumin and to immunoglobulin from 9.2 to 27.6 mg of alcohol/g of&#13;
protein, respectively. The proposed method was applied successfully in industrial batches for the determination of the alcohol content as impurity.
</description>
</item>
<item rdf:about="https://hdl.handle.net/10481/27467">
<title>Formulation and evaluation of sustained release microspheres of rosin containing aceclofenac</title>
<link>https://hdl.handle.net/10481/27467</link>
<description>Formulation and evaluation of sustained release microspheres of rosin containing aceclofenac
Lakshmana Prabu, S.; Shirwaikar, A.A.; Shirwaikar, A.; Kumari, A.
Aceclofenac was microencapsulated using rosin by o/w emulsion solvent evaporation&#13;
technique. The effect of three formulation variables including the drug:polymer ratio,&#13;
emulsifier (polyvinyl alcohol) concentration and organic solvent (dichloromethane) volume&#13;
were examined. The prepared batches were characterized for microspheres particle size&#13;
distribution, encapsulation efficiency and in vitro release behavior. The study reveals that&#13;
drug:polymer ratio had a considerable effect on the entrapment efficiency, however particle&#13;
size distribution of microspheres was more dependent on the volume of dichloromethane and&#13;
polyvinyl alcohol concentration rather than on the drug: polymer ratio. Drug, polymer&#13;
concentrations were varied to obtain optimum release profile for sustaining the action of the drug.
</description>
</item>
<item rdf:about="https://hdl.handle.net/10481/27466">
<title>Drug delivery systems based on poly(e-caprolactone) for cancer treatment</title>
<link>https://hdl.handle.net/10481/27466</link>
<description>Drug delivery systems based on poly(e-caprolactone) for cancer treatment
Sáez-Fernández, E.; Ruiz Martínez, María A.; Arias Mediano, José Luis
Chemotherapy agents have little or no specificity over cancer cells, resulting in low therapeutic concentrations at the tumor site (a consequence of a broad systemic distribution),&#13;
and severe side effects. With the aim of avoiding cancer therapy failure, several approaches&#13;
such as design of new anticancer drugs, chemical engineering of conventional drugs and&#13;
development of drug delivery systems have been proposed. The objective is to enhance drug&#13;
localization at the tumor region (by controlling its biodistribution profile) and, therefore, to&#13;
increase the anti-tumor efficacy (even in multi-drug resistant tumors), while reducing&#13;
systemic side effects. One of the most promising approaches to the problem is the&#13;
development of drug nanocarriers based on the polymer poly(e-caprolactone). In this review&#13;
we will focus our attention on these polymeric colloids, particularly on the most significant&#13;
characteristics and formulation procedures, and on their use as nanoplatforms for the delivery&#13;
of chemotherapy agents to the tumor site. Furthermore, the most recent in vitro and in vivo investigations on the subject are extensively reviewed.
</description>
</item>
<item rdf:about="https://hdl.handle.net/10481/27464">
<title>Adjudication of new community pharmacies: comparison of ranking criteria</title>
<link>https://hdl.handle.net/10481/27464</link>
<description>Adjudication of new community pharmacies: comparison of ranking criteria
Ríos, L.M.; Garrigues, T.M.; Martín, A.; Muelas, J.A.
This article studies the differences between the models of candidate classification for the adjudication of new pharmacies in the different Spanish self-governing regions. The objective of this study is to analyze the profile of the selected professional. Generally, the ranking takes into account the professional activity as pharmacist, the pre-graduate formation as well as the postgraduate, with different weights. Some of the 15 autonomies include as merits the cooficial languages, an optional written test and special situations as unemployment.&#13;
In general, the criteria try to find out the best profile of pharmacist based on the professional experience and the postgraduate formation.
</description>
</item>
</rdf:RDF>
