Formulation and Evaluation of Transdermal Patches of Glizpizide
نویسنده
چکیده
Drug Delivery through skin would provide a useful alternative to oral delivery, which has numerous side effects. Therefore, the present investigation was aimed to develop sustained release transdermal therapeutics system containing Glipizide with varying ratios of HPMC & PVPK30 using solvent evaporation technique. Ten different formulations were prepared keeping the concentration of Glipizide constant as 45mg in each formulation. The films were developed and evaluated for thickness, weight variation, percent moisture absorption, percent moisture loss, folding endurance, drug content and in vitro drug dissolution studies. Finally, on the basis of best release one of the formulations was selected for further kinetic studies which exhibited that release rate followed Fickian’s diffusion law. The selected formulation showed no sign of irritation when studied using mice skin. Finally, it was concluded that Glipizide transdermal patch could improve the bioavailability of the drug by avoiding its first pass metabolism.
منابع مشابه
Optimization of In-vitro Permeation Pattern of Ketorolac Tromethamine Transdermal Patches
The present study was undertaken to develop a suitable transdermal matrix patch of ketorolac tromethamine with different proportions of polyvinyl pyrrolidone (PVP) and ethyl cellulose (EC) using a D-optimal mixture design. The prepared transdermal patches were subjected to different physicochemical evaluation. The surface topography of the patches was examined by scanning electron microscopy (S...
متن کاملOptimization of In-vitro Permeation Pattern of Ketorolac Tromethamine Transdermal Patches
The present study was undertaken to develop a suitable transdermal matrix patch of ketorolac tromethamine with different proportions of polyvinyl pyrrolidone (PVP) and ethyl cellulose (EC) using a D-optimal mixture design. The prepared transdermal patches were subjected to different physicochemical evaluation. The surface topography of the patches was examined by scanning electron microscopy (S...
متن کاملDevelopment and Optimization of Transdermal System of Lisinopril dehydrate: Employing Permeation Enhancers
Lisinopril dihydrate (angiotensin converting enzyme inhibitor) is a lysine derivative of enalaprilat and does not require hydrolysis to exert pharmacological activity. It has an extensive hepatic first pass metabolism resulting in a bioavailabil-ity of 6-60%. To overcome the poor bioavailability of the drug, transdermal patches have been prepared. The present study also aims at optimizati...
متن کاملFormulation, In-vitro Evaluations and Skin Irritation Study of Losartan Potassium Transdermal Patches
Losartan potassium is a well known orally active non-peptide angiotensin II receptor antagonist. Losartan potassium and its principle active metabolites block the vasoconstrictor and aldosterone secreting effect of angiotensin II by selectively blocking the binding of angiotensin II to AT1 receptors. The drug is reported to promote the decrease in ventricular hypertrophy, salt ...
متن کاملPravastatin transdermal patch: Effect of the formulation and length of microneedles on in- vitro percutaneous absorption studies.
Transdermal patches loaded with pravastatin was previously characterized in another published study by Serrano-Castañeda et al; 2015. These transdermal patches (TP) were generated by the plate casting technique, the in vitro percutaneous absorption studies of TP were evaluated for three different formulations of TP with different quantities of Pluronic F-127 (PF-127): i) without PF-127 (TP W), ...
متن کامل