Microparticulate dosage form for non-steroidal anti-inflammatory drugs: In vitro and in vivo evaluation

Tamilvanan Shunmugaperumal

Published by LAP LAMBERT Academic Publishing, 2010
ISBN 10: 3838395425 / ISBN 13: 9783838395425
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Synopsis: Indomethacin (IMC)-and ibuprofen (IBP)-loaded polystyrene microparticles were prepared by emulsion- solvent evaporation method from an aqueous system. Comparing the in vitro drug release profiles obtained from microparticles and marketed SR products allow the selection of an optimized formulation for IMC and IBP. Bioavailability studies in human volunteers indicate that while no differences among the pharmacokinetic parameters were evidenced between the optimized and SR- formulations of IMC, all parameters except ka and ke of the optimized IBP formulation were lower than that those of the SR-formulation. Although statistically significant in vitro: in vivo correlations were observed individually for the optimized and for the SR- formulations, values of retard quotient (R?), revealed an almost same and a lower retardation for the optimized IMC and IBP formulations, respectively. With this coverage on in vitro and in vivo evaluation of microparticles, this book is an essential reference for researchers in pharmaceutical industry who develop oral microparticulate dosage forms.

About the Author: Tamilvanan Shunmugaperumal, Ph.D: Studied Pharmacy at Annamalai University, Madras Medical College and Jadavpur University, India. Post-doctoral fellow at Hebrew University of Jerusalem, Israel and University of Antwerp, Belgium. Currently he works in International Medical University, Kuala Lumpur, Malaysia.

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Title: Microparticulate dosage form for ...
Publisher: LAP LAMBERT Academic Publishing
Publication Date: 2010
Binding: Paperback
Book Condition: Good

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Book Description LAP Lambert Acad. Publ. Aug 2010, 2010. Taschenbuch. Condition: Neu. Neuware - Indomethacin (IMC)-and ibuprofen (IBP)-loaded polystyrene microparticles were prepared by emulsion- solvent evaporation method from an aqueous system. Comparing the in vitro drug release profiles obtained from microparticles and marketed SR products allow the selection of an optimized formulation for IMC and IBP. Bioavailability studies in human volunteers indicate that while no differences among the pharmacokinetic parameters were evidenced between the optimized and SR- formulations of IMC, all parameters except ka and ke of the optimized IBP formulation were lower than that those of the SR-formulation. Although statistically significant in vitro: in vivo correlations were observed individually for the optimized and for the SR- formulations, values of retard quotient (R ), revealed an almost same and a lower retardation for the optimized IMC and IBP formulations, respectively. With this coverage on in vitro and in vivo evaluation of microparticles, this book is an essential reference for researchers in pharmaceutical industry who develop oral microparticulate dosage forms. 160 pp. Englisch. Seller Inventory # 9783838395425

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Book Description LAP Lambert Acad. Publ. Aug 2010, 2010. Taschenbuch. Condition: Neu. Neuware - Indomethacin (IMC)-and ibuprofen (IBP)-loaded polystyrene microparticles were prepared by emulsion- solvent evaporation method from an aqueous system. Comparing the in vitro drug release profiles obtained from microparticles and marketed SR products allow the selection of an optimized formulation for IMC and IBP. Bioavailability studies in human volunteers indicate that while no differences among the pharmacokinetic parameters were evidenced between the optimized and SR- formulations of IMC, all parameters except ka and ke of the optimized IBP formulation were lower than that those of the SR-formulation. Although statistically significant in vitro: in vivo correlations were observed individually for the optimized and for the SR- formulations, values of retard quotient (R ), revealed an almost same and a lower retardation for the optimized IMC and IBP formulations, respectively. With this coverage on in vitro and in vivo evaluation of microparticles, this book is an essential reference for researchers in pharmaceutical industry who develop oral microparticulate dosage forms. 160 pp. Englisch. Seller Inventory # 9783838395425

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Book Description LAP Lambert Acad. Publ. Aug 2010, 2010. Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Neuware - Indomethacin (IMC)-and ibuprofen (IBP)-loaded polystyrene microparticles were prepared by emulsion- solvent evaporation method from an aqueous system. Comparing the in vitro drug release profiles obtained from microparticles and marketed SR products allow the selection of an optimized formulation for IMC and IBP. Bioavailability studies in human volunteers indicate that while no differences among the pharmacokinetic parameters were evidenced between the optimized and SR- formulations of IMC, all parameters except ka and ke of the optimized IBP formulation were lower than that those of the SR-formulation. Although statistically significant in vitro: in vivo correlations were observed individually for the optimized and for the SR- formulations, values of retard quotient (R ), revealed an almost same and a lower retardation for the optimized IMC and IBP formulations, respectively. With this coverage on in vitro and in vivo evaluation of microparticles, this book is an essential reference for researchers in pharmaceutical industry who develop oral microparticulate dosage forms. 160 pp. Englisch. Seller Inventory # 9783838395425

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