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Development of Self Microemulsifying Drug Delivery System: Preparation and evaluation of Lovastatin Self Microemulsifying Drug Delivery System - Softcover
Synopsis
Nearly 40% of new drug candidates exhibit low solubility in water, which leads to poor oral bioavailability, high intra- and inter-subject variability and lack of dose proportionality. Modification of the physicochemical properties, such as salt formation and particle size reduction of the compound may be one approach to improve the dissolution rate of the drug. However, these methods have their own limitations. In recent years, much attention has focused on lipid based formulations to improve the oral bioavailability of poorly water soluble drugs. In fact, the most popular approach is the incorporation of the drug compound into inert lipid vehicles such as oils, surfactant dispersions, self-emulsifying formulations, emulsions and liposomes with particular emphasis on self-microemulsifying drug delivery systems (SMEDDS).
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About the Author
Mr. Maulik J. Patel (Assistant Professor, Pharmaceutics Department), Dr. Sanjay S. Patel, (Associate Professor, Pharmaceutics Department) and Dr. Natvarlal M. Patel (Principal) working in Shri B. M. Shah College of Pharmaceutical Education and Research, Modasa – 383315, India
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Development of Self Microemulsifying Drug Delivery System
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LAP LAMBERT Academic Publishing Mai 2011, 2011
ISBN 10: 3844331824
ISBN 13: 9783844331820
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Nearly 40% of new drug candidates exhibit low solubility in water, which leads to poor oral bioavailability, high intra- and inter-subject variability and lack of dose proportionality. Modification of the physicochemical properties, such as salt formation and particle size reduction of the compound may be one approach to improve the dissolution rate of the drug. However, these methods have their own limitations. In recent years, much attention has focused on lipid based formulations to improve the oral bioavailability of poorly water soluble drugs. In fact, the most popular approach is the incorporation of the drug compound into inert lipid vehicles such as oils, surfactant dispersions, self-emulsifying formulations, emulsions and liposomes with particular emphasis on self-microemulsifying drug delivery systems (SMEDDS). 104 pp. Englisch. Seller Inventory # 9783844331820
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Development of Self Microemulsifying Drug Delivery System
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LAP LAMBERT Academic Publishing, 2011
ISBN 10: 3844331824
ISBN 13: 9783844331820
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Patel Mr.MaulikMr. Maulik J. Patel (Assistant Professor, Pharmaceutics Department), Dr. Sanjay S. Patel, (Associate Professor, Pharmaceutics Department) and Dr. Natvarlal M. Patel (Principal) working in Shri B. M. Shah College of . Seller Inventory # 5473562
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Development of Self Microemulsifying Drug Delivery System
Published by
LAP LAMBERT Academic Publishing Mai 2011, 2011
ISBN 10: 3844331824
ISBN 13: 9783844331820
New
Taschenbuch
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germany
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Taschenbuch. Condition: Neu. Neuware -Nearly 40% of new drug candidates exhibit low solubility in water, which leads to poor oral bioavailability, high intra- and inter-subject variability and lack of dose proportionality. Modification of the physicochemical properties, such as salt formation and particle size reduction of the compound may be one approach to improve the dissolution rate of the drug. However, these methods have their own limitations. In recent years, much attention has focused on lipid based formulations to improve the oral bioavailability of poorly water soluble drugs. In fact, the most popular approach is the incorporation of the drug compound into inert lipid vehicles such as oils, surfactant dispersions, self-emulsifying formulations, emulsions and liposomes with particular emphasis on self-microemulsifying drug delivery systems (SMEDDS).Books on Demand GmbH, Überseering 33, 22297 Hamburg 104 pp. Englisch. Seller Inventory # 9783844331820
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Development of Self Microemulsifying Drug Delivery System : Preparation and evaluation of Lovastatin Self Microemulsifying Drug Delivery System
Published by
LAP LAMBERT Academic Publishing, 2011
ISBN 10: 3844331824
ISBN 13: 9783844331820
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Nearly 40% of new drug candidates exhibit low solubility in water, which leads to poor oral bioavailability, high intra- and inter-subject variability and lack of dose proportionality. Modification of the physicochemical properties, such as salt formation and particle size reduction of the compound may be one approach to improve the dissolution rate of the drug. However, these methods have their own limitations. In recent years, much attention has focused on lipid based formulations to improve the oral bioavailability of poorly water soluble drugs. In fact, the most popular approach is the incorporation of the drug compound into inert lipid vehicles such as oils, surfactant dispersions, self-emulsifying formulations, emulsions and liposomes with particular emphasis on self-microemulsifying drug delivery systems (SMEDDS). Seller Inventory # 9783844331820
Quantity: 1 available
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Development of Self Microemulsifying Drug Delivery System: Preparation and evaluation of Lovastatin Self Microemulsifying Drug Delivery System
Published by
LAP LAMBERT Academic Publishing, 2011
ISBN 10: 3844331824
ISBN 13: 9783844331820
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