Se analizó el efecto de un aglutinante, polivinilpirrolidona (PVP), y de un desintegrante, almidón,sobre el proceso de disolución de comprimidos de paracetamol, calculándose una serie de parámetros cinéticos con el objeto de estimar la biodisponibilidad in vitro de los mismos. Los resultados muestran un aumento de la velocidad de disolución del paracetamol cuando el PVP es adicionado como solución a la formulación y una disminución cuando la concentración de almidón es menor. Se realizó un estudio de bioequivalencia comparando los resultados obtenidos con los de otras formulaciones de circulación en el mercado farmacéutico argentino, encontrándose que no todos los productos analizados son bioequivalentes entre sí.The effects of polyvinilpyr...
Tablets of paracetamol BP prepared with purified starch obtained from the bulbs of locally cultivate...
Purpose: The individual and interaction effects of nature of binder (N), concentration of binder (C)...
The clinical effectiveness of tablets and other pharmaceutical dosage forms of drug depends on at le...
Se analizó el efecto de un aglutinante (polivinilpirrolidona, PVP), de un disgregrante (almidón) y d...
Objective: To study the effects of three formulation variables (PVP, stearic acid and Avicel PH101) ...
With the purpose of evaluating the behavior of different polymers employed as binders in small-diame...
A 23 factorial experimental design has been used to quantitatively study individual and interaction ...
The purpose of this investigation was to study the dissolution behavior of paracetamol and ibuprofen...
The binding and disintegrating properties of Godare (Colcosia esculenta) starch in paracetamol tab...
ABSTRACT: Ten brands of commercial paracetamol suspensions were investigated for their dissolution c...
Abstract— The effect of cyclodextrin (β‐CD) on the solubility and dissolution rate of various parace...
Purpose: The individual and interaction effects of nature of binder (N), concentration of binder (C)...
This study was carried out to comparatively evaluate the tableting and release characteristics of pa...
A 2³ factorial experimental design has been used to quantitatively study individual and interaction ...
Trabalho Final de Mestrado Integrado, Ciências Farmacêuticas, Universidade de Lisboa, Faculdade de F...
Tablets of paracetamol BP prepared with purified starch obtained from the bulbs of locally cultivate...
Purpose: The individual and interaction effects of nature of binder (N), concentration of binder (C)...
The clinical effectiveness of tablets and other pharmaceutical dosage forms of drug depends on at le...
Se analizó el efecto de un aglutinante (polivinilpirrolidona, PVP), de un disgregrante (almidón) y d...
Objective: To study the effects of three formulation variables (PVP, stearic acid and Avicel PH101) ...
With the purpose of evaluating the behavior of different polymers employed as binders in small-diame...
A 23 factorial experimental design has been used to quantitatively study individual and interaction ...
The purpose of this investigation was to study the dissolution behavior of paracetamol and ibuprofen...
The binding and disintegrating properties of Godare (Colcosia esculenta) starch in paracetamol tab...
ABSTRACT: Ten brands of commercial paracetamol suspensions were investigated for their dissolution c...
Abstract— The effect of cyclodextrin (β‐CD) on the solubility and dissolution rate of various parace...
Purpose: The individual and interaction effects of nature of binder (N), concentration of binder (C)...
This study was carried out to comparatively evaluate the tableting and release characteristics of pa...
A 2³ factorial experimental design has been used to quantitatively study individual and interaction ...
Trabalho Final de Mestrado Integrado, Ciências Farmacêuticas, Universidade de Lisboa, Faculdade de F...
Tablets of paracetamol BP prepared with purified starch obtained from the bulbs of locally cultivate...
Purpose: The individual and interaction effects of nature of binder (N), concentration of binder (C)...
The clinical effectiveness of tablets and other pharmaceutical dosage forms of drug depends on at le...