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Short Article Open Access
An attempt was made to compare and assess the permeability characteristics of selected drug molecules by varying lipophilicity and molecular weight using in vitro diffusion assembly and everted small intestinal sac model. Apparent permeability coefficient, flux, permeability coefficient and enhancement ratio of selected drug molecules through both the models were compared. The permeation data was compared with physicochemical properties including solubility parameter of drug molecules. In vitro data was found to be higher than the data obtained from everted sac model. Permeation of drugs through everted sac model was significantly enhanced by incorporation of sodium taurocholate (1%), which could be correlated with in vitro diffusion data.
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Author(s): Sarasija Suresh H P Joshi