Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon

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Due to the risk of HIV infection, a rectal microbicide (RM) is needed as a prophylactic. This clinical study evaluated the pharmacokinetics luminal and pharmacodynamics of four candidate formulations as MR vehicles. Eight men participated in this randomized, partially blinded comparative study. Form...

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Detalles Bibliográficos
Autor: Leyva Hurtado, Francisco José
Formato: tesis de maestría
Fecha de Publicación:2012
Institución:Superintendencia Nacional de Educación Superior Universitaria
Repositorio:Registro Nacional de Trabajos conducentes a Grados y Títulos - RENATI
Lenguaje:inglés
OAI Identifier:oai:renati.sunedu.gob.pe:renati/7031
Enlace del recurso:https://renati.sunedu.gob.pe/handle/sunedu/3482021
Nivel de acceso:acceso abierto
Materia:Antiinfecciosos
Enema
VIH
Prevención de enfermedades
Colon
Farmacocinética
Acciones farmacológicas
https://purl.org/pe-repo/ocde/ford#3.01.05
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dc.title.es_PE.fl_str_mv Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
dc.title.alternative.es_PE.fl_str_mv Farmacocinética luminal, farmacodinámica y aceptabilidad de cuatro candidatos a vehículos microbicidas rectales en el colon distal
title Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
spellingShingle Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
Leyva Hurtado, Francisco José
Antiinfecciosos
Enema
VIH
Prevención de enfermedades
Colon
Farmacocinética
Acciones farmacológicas
https://purl.org/pe-repo/ocde/ford#3.01.05
title_short Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
title_full Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
title_fullStr Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
title_full_unstemmed Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
title_sort Luminal Pharmacokinetics, Pharmacodynamics, and Acceptability of Four Rectal Microbicide Vehicle Candidates in the Distal Colon
author Leyva Hurtado, Francisco José
author_facet Leyva Hurtado, Francisco José
author_role author
dc.contributor.advisor.fl_str_mv Hendrix, Craig W.
Flexner, Charles W.
dc.contributor.author.fl_str_mv Leyva Hurtado, Francisco José
dc.subject.es_PE.fl_str_mv Antiinfecciosos
Enema
VIH
Prevención de enfermedades
Colon
Farmacocinética
Acciones farmacológicas
topic Antiinfecciosos
Enema
VIH
Prevención de enfermedades
Colon
Farmacocinética
Acciones farmacológicas
https://purl.org/pe-repo/ocde/ford#3.01.05
dc.subject.ocde.es_PE.fl_str_mv https://purl.org/pe-repo/ocde/ford#3.01.05
description Due to the risk of HIV infection, a rectal microbicide (RM) is needed as a prophylactic. This clinical study evaluated the pharmacokinetics luminal and pharmacodynamics of four candidate formulations as MR vehicles. Eight men participated in this randomized, partially blinded comparative study. Formulations aqueous fluid (AF), aqueous gel (AG), lipid fluid (LF) and lipid gel (LG), were mixed with diethylenetriaminepentaacetic acid labeled with Technetium-99m and administered intrarectically. One hour later, colon biopsies and brushings were obtained using sigmoidoscopy. SPEC/CT images were obtained at 2, 4, and 24 hours. Colonic distribution was described using concentration-distance (Dmax) parameters. Colonic histology did not find differences in epithelial denudation. Luminal concentrations of AG and LF and tissue concentrations of LF showed a significant decrease (p<0.05) compared to AF. The permeability of lipid products was significantly higher than in aqueous products (p<0.05). Colonic distribution showed a significantly shorter Dmax at 4-hours than at 2-hours (p=0.014). LF had a significantly shorter Dmax than AF (p=0.009). This study has shown that AF, AG and LG formulations do not damage the colonic epithelium. All formulations showed a decrease in colonic distribution over time. The lipid formulations showed greater permeability than the aqueous ones.
publishDate 2012
dc.date.accessioned.none.fl_str_mv 2023-11-10T14:07:17Z
dc.date.available.none.fl_str_mv 2023-11-10T14:07:17Z
dc.date.issued.fl_str_mv 2012-08
dc.type.es_PE.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.language.iso.es_PE.fl_str_mv eng
language eng
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dc.publisher.es_PE.fl_str_mv Johns Hopkins University
dc.publisher.country.es_PE.fl_str_mv US
dc.source.es_PE.fl_str_mv Superintendencia Nacional de Educación Superior Universitaria - SUNEDU
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spelling Hendrix, Craig W.Flexner, Charles W.Leyva Hurtado, Francisco José2023-11-10T14:07:17Z2023-11-10T14:07:17Z2012-08https://renati.sunedu.gob.pe/handle/sunedu/3482021Due to the risk of HIV infection, a rectal microbicide (RM) is needed as a prophylactic. This clinical study evaluated the pharmacokinetics luminal and pharmacodynamics of four candidate formulations as MR vehicles. Eight men participated in this randomized, partially blinded comparative study. Formulations aqueous fluid (AF), aqueous gel (AG), lipid fluid (LF) and lipid gel (LG), were mixed with diethylenetriaminepentaacetic acid labeled with Technetium-99m and administered intrarectically. One hour later, colon biopsies and brushings were obtained using sigmoidoscopy. SPEC/CT images were obtained at 2, 4, and 24 hours. Colonic distribution was described using concentration-distance (Dmax) parameters. Colonic histology did not find differences in epithelial denudation. Luminal concentrations of AG and LF and tissue concentrations of LF showed a significant decrease (p<0.05) compared to AF. The permeability of lipid products was significantly higher than in aqueous products (p<0.05). Colonic distribution showed a significantly shorter Dmax at 4-hours than at 2-hours (p=0.014). LF had a significantly shorter Dmax than AF (p=0.009). This study has shown that AF, AG and LG formulations do not damage the colonic epithelium. All formulations showed a decrease in colonic distribution over time. The lipid formulations showed greater permeability than the aqueous ones.Debido al riesgo de infección por HIV, se necesita un microbicida rectal (MR) como profiláctico. Este estudio clínico evaluó la farmacocinética luminal y farmacodinamia de cuatro formulaciones candidatas como vehículos de MR. Ocho hombres participaron en este estudio comparativo, aleatorizado y parcialmente ciego. Formulaciones fluido acuoso (AF), gel acuoso (AG), fluido lipídico (LF) y gel lipídico (LG), fueron mezcladas con ácido dietilentriaminopentaacético marcado con Tecnecio-99m y administradas vía intrarrectal. Una hora después, mediante sigmoidoscopia se obtuvieron biopsias de colon y cepillados. Imágenes SPEC/CT se obtuvieron a las 2, 4 y 24 horas. Distribución colónica se describió mediante parámetros de concentración-distancia (Dmax). Histología colónica no encontró diferencias en denudación epitelial. Concentraciones luminales de AG y LF y concentraciones tisulares de LF mostraron una disminución significativa (p<0.05) en comparación con AF. La permeabilidad de productos lipídicos fue significativamente mayor que en los acuosos (p<0.05). Distribución colónica mostró una Dmax a las 4-horas significativamente más corta que a las 2-horas (p=0.014). LF tuvo una Dmax significativamente más corta que el AF (p=0,009). Este estudio ha demostrado que las formulaciones AF, AG y LG no dañan el epitelio colónico. Todas las formulaciones mostraron disminución en la distribución colónica con el tiempo. Las formulaciones lipídicas mostraron mayor permeabilidad que las acuosas.Estados Unidos. The Johns Hopkins University / National Institutes of Health. 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