Article
Authorship
Date
2018
Publishing House and Editing Place
SPRINGER
Magazine
AAPS PHARMSCITECH,
vol. 19
(pp. 2629-2638)
SPRINGER
Summary
Information provided by the agent in
SIGEVA
The aim of this work was to predict the permeability of two model drugs, sulfamerazine (SMR) and indomethacin (INM), and to determine the effect on their apparent permeabilities by complexation with cyclodextrins and/or meglumine or incorporation in microemulsions. Permeation experiments were performed using two-chamber diffusion cells with a new composition of bio-mimetic membrane composed of an 80% of Lipoid® S100 and a 20% of cholesterol in n-octanol 10% w/w solution, at 37 ± 0.50...
The aim of this work was to predict the permeability of two model drugs, sulfamerazine (SMR) and indomethacin (INM), and to determine the effect on their apparent permeabilities by complexation with cyclodextrins and/or meglumine or incorporation in microemulsions. Permeation experiments were performed using two-chamber diffusion cells with a new composition of bio-mimetic membrane composed of an 80% of Lipoid® S100 and a 20% of cholesterol in n-octanol 10% w/w solution, at 37 ± 0.50C and 14000 rpm. The predictive capacity of the permeability of passive diffusion absorbed compounds was evaluated using 20 drug standards, and showed an exponential correlation between the apparent permeability coefficients (Papp) and the fraction absorbed percentages in humans (Fa%), with an R square value of 0.67942 and a constant value of -4.1 ± 0.8. SMR and INM, were classified as CLASS II, according to the Biopharmaceutical Classification System (BCS). These drugs, were complexed and incorporated in microemulsions. The Fa% from all the drug products were higher than 90%. SMR in the complexes and both drugs in microemulsions were classified as highly soluble. Thus, SMR and INM incorporated in these pharmaceutical products could be classified as CLASS I.
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Key Words
COMPLEXESMICROEMULSIONSPERMEABILITYPASSIVE DIFFUSION ABSORBED COMPOUNDSARTIFICIAL MEMBRANES