The present investigation aimed at formulation, and evaluation of
vesicular drug carrier system liquid crystalline proliposomes for
transdermal delivery of antifungal agent, griseofulvin. Liquid
crystalline proliposomal gel (LCPG) formulations of griseofulvin
were prepared, and characterized for vesicles shape, size,
entrapment efficiency, and drug permeation across pig ear skin. The
effects of different formulation variables (type of alcohol, type
and concentration of surfactant) on transdermal permeability
profile were assessed. The optimized LCPG formulation showed
enhanced In Vitro skin permeation flux of 10.705 0.052 ug/cm2/hr as
compared to 0.028 0.02 ug/cm2/hr for plain drug solution in water.
Results indicated that the optimized proliposomal formulation of
griseofulvin had better skin permeation potential than plain drug
solution in water."
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