Solid Self Emulsifying Drug Delivery System of Glibenclamide

 
9783659540264: Solid Self Emulsifying Drug Delivery System of Glibenclamide
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The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique.

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Mrs Maria Saifee is working as Associate Professor (Pharmaceutics) in Y.B.chavan college of Pharmacy, Aurangabad. She has got 15 yrs of vast research and teaching experience.

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Saifee, Maria / Zarekar, Sharda
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Book Description Condition: New. Publisher/Verlag: LAP Lambert Academic Publishing | The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique. | Format: Paperback | Language/Sprache: english | 120 pp. Seller Inventory # K9783659540264

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Book Description LAP Lambert Academic Publishing Jul 2014, 2014. Taschenbuch. Condition: Neu. Neuware - The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique. 120 pp. Englisch. Seller Inventory # 9783659540264

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Book Description LAP Lambert Academic Publishing Jul 2014, 2014. Taschenbuch. Condition: Neu. Neuware - The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique. 120 pp. Englisch. Seller Inventory # 9783659540264

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Book Description LAP Lambert Academic Publishing, United States, 2014. Paperback. Condition: New. Language: English . Brand New Book ***** Print on Demand *****.The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique. Seller Inventory # AAV9783659540264

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Book Description LAP Lambert Academic Publishing Jul 2014, 2014. Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Neuware - The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS .Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and % transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites.Thus Solid SEEDS can be used as a means of dissolution enhancement technique. 120 pp. Englisch. Seller Inventory # 9783659540264

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Book Description LAP LAMBERT Academic Publishing. Paperback. Condition: New. 120 pages. Dimensions: 8.7in. x 5.9in. x 0.3in.The study was aimed to develop solid self micro emulsifying drug delivery system (S-SEDDS) for dissolution enhancement of model drug Glibenclamide using Aerosil 200 as solid carrier. SEDDS was prepared using oil, surfactant and cosurfactant respectively. Pseudo ternary phase diagram was used to identify micro emulsion region for formulating stable SEEDS . Prepared SEDDS was evaluated for turbidity measurement, globule size and zeta potential, viscosity determination and transmittance. S-SEDDS was prepared by adsorption technique using Aerosil 200 as solid carrier. Prepared S-SEDDS was evaluated for flow properties, drug content, FTIR, SEM, DSC and in-vitro dissolution study. Results showed that prepared liquid SEDDS passed all evaluation tests. S-SEDDS showed good flow property and drug content. From the experiment, it is clear that even after conversion of the liquid SEDDS into the solid SEEDS, their is no significant alteration in its propertites. Thus Solid SEEDS can be used as a means of dissolution enhancement technique. This item ships from multiple locations. Your book may arrive from Roseburg,OR, La Vergne,TN. Paperback. Seller Inventory # 9783659540264

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