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Bioavailability and bioequivalence in pharmaceutical technology

Bioavailability and bioequivalence in pharmaceutical technology

Bioavailability and Bioequivalence in Pharmaceutical Technology

Author Tapan Kumar Pal, M Ganesan

EditionRevised Edition

Year2004

ISBN9788123911588

MRP: ₹495

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Descriptions

Descriptions

The concept of bioavailability and its study methodology in human volunteers have been discussed in detail with a special emphasis on protocol preparation, volunteer screening, informed consent, inclusion and exclusion criteria and study of pathological parameters prior to undertaking any bioequivalence study. Various methods of sample preparation and extraction of drug from plasma have been illustrated by different methods. The sophisticated techniques of solid phase extraction (SPE) system have been proved to be most simple, sensitive and time-saving. The different dimensions of its application and procedures have been highlighted. The procedures for evaluation of pharmacokinetic parameters (Cmax, Tmax & AUC) and their interpretation have been illustrated with methodical approach. The application of microdialysis in bioavailability study as well as ocular kinetics and drug delivery system of ophthalmic medicines have also been discussed in this book.

Specifications

Specifications

ISBN	9788123911588
Published Year	2004
Binding	Hardcover
Subject	Pharmaceutical Technology
Pages	159
Weight	0.3 (In Kg)
Dimension	17 × 5 × 1.2
Readership	BPharma

About the Author

Tapan Kumar Pal

Tapan Kumar Pal

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M Ganesan

M Ganesan

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