Por favor, use este identificador para citar o enlazar este ítem: http://repositorio.pediatria.gob.mx:8180/handle/20.500.12103/2346
Título : Effect of severe protein-calorie malnutrition on the penetration kinetics of trimethoprim and sulfamethoxazole to the deep tissues of Wistar rats
Creador: Lares Asseff, Ismael
Nivel de acceso: Open access
Palabras clave : Antiinfecciosos aministración y dosis - administración y dosis
Antiinfecciosos - farmacocinética
Proteínas en la Dieta - administración y dosis
Esquema de Medicación
Riñón - metabolismo
hígado - metabolismo
pulmón - metabolismo
Desnutrición
Combinación Trimetoprim y Sulfametoxazol - administración y dosis
Combinación Trimetoprim y Sulfametoxazol - Farmacocinética
Anti-Infective Agents - administration & dosage
Anti-Infective Agents - pharmacokinetics
Dietary Proteins - administration & dosage
Drug Administration Schedule
Kidney - metabolism
Liver - metabolism
Lung - metabolism
Malnutrition
Trimethoprim, Sulfamethoxazole Drug Combination - administration & dosage
Trimethoprim, Sulfamethoxazole Drug Combination - pharmacokinetics
Descripción : This study shows the effect that severe malnourishment has on the kinetics of antibiotic penetration in tissues. A total of 104 male Wistar rats, 21 days old, were randomly divided into eight groups. Five groups of experimental rats were severely malnourished (SM) and three further groups were considered well-nourished control groups (WN). A single dose of trimethoprim-sulfamethoxazole (TMP-SMX) was administered intraperitoneally. Blood samples were taken by heart puncture and five organs were extracted 0-24 h after the administration of the drug. HPLC was used to assess the amount of trimethoprim and sulfamethoxazole in fluids. The elimination half-life for trimethoprim from plasma was longer in SM rats with a median of 3.15 h; in WN rats, it was 0.390 h. Clearance was slower in SM rats: 646.72 mL μg-1h-1 vs 3036.38 mL μg-1h-1 in WN rats (P<0.05). Tissue penetration was much higher for trimethoprim, with penetration indexes of 0.80-5.66 in WN rats, compared with 0.35-2.14 in SM rats. In the case of sulfamethoxazole, penetration indexes were 0.029-1.13 for WN and 0.075-0.657 for SM rats. Similarly, the penetration ratio to muscle and heart tissue was lower in SM rats. However, penetration to kidney, lung, liver and spleen was greater in SM rats. It is evident that severe SM decreases the capacity of trimethoprim more importantly than sulfamethoxazole biotransformation.
Colaborador(es) u otros Autores: Pérez MG
Camacho GA
Toledo AR
del Carmen López M
Guillé AJ
Sosa MG
Fecha de publicación : 2003
Tipo de publicación: Artículo
Formato: pdf
Identificador del Recurso : 10.1211/0022357021026
Fuente: Journal of Pharmacy and Pharmacology 55(4):469 - 477
URI : http://repositorio.pediatria.gob.mx:8180/handle/20.500.12103/2346
Idioma: eng
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