FORMULATION AND INVITRO EVALUATION OF ETHOSOMAL GELS CONTAINING GLIBENCLAMIDE AS THE MODEL DRUG
Sd Riyaz Hussain Chistia*, Dr. Pawan Kumar and Dr. Parwez Alam.
The process Touitou et al (2000) defined was used with little change to prepare various ethosomal formulations with different levels of IPA (20% to 40%) and sonicity. It was simple and reproductible techniques. The prepared and discrete ethosomes have been developed. However, ethosomes are more uniform in size and small, necessary for skin penetration by the process of sonication. When the efficiency of the trap was compared, ethosomes containing 30 percent w/w IPA, which were generated by sonication, displayed the highest value with respect to all others; Therefore, with 30 percent w/w IPA as the best formula for all other aspects, ethosomally provided by sonicity was completed. In all formulations, GF6 demonstrated full release of the drugs in 1,440 min compared to other formulations. The in vitro release decreased with increased concentrations of polymer and copolymer. Centered on the research findings of the drug release process the drug discharge followed the non-fickian diffusion mechanism by formulations and followed the first order kinetics.
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