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Liquid Chromatography Pharmaceutical Development (3 results)
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Liquid Chromatography in Pharmaceutical Development: An Introduction
Seller: Zubal-Books, Since 1961, Cleveland, OH, U.S.A.
Seller rating 5 out of 5 stars
Condition: Good. 496 pp., Hardcover, ex library, front cover discolored else text clean and binding tight. - If you are reading this, this item is actually (physically) in our stock and ready for shipment once ordered. We are not bookjackers. Buyer is responsible for any additional duties, taxes, or fees required by recipient's country.
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Analytical Method development by Liquid Chromatography | Development and Validation of Analytical Methods for the Assay of Selected Drugs in Pharmaceutical Dosage forms and Biological fluids
Language: English
Published by LAP LAMBERT Academic Publishing, 2011
ISBN 10: 3844328696 ISBN 13: 9783844328691
Taschenbuch. Condition: Neu. Analytical Method development by Liquid Chromatography | Development and Validation of Analytical Methods for the Assay of Selected Drugs in Pharmaceutical Dosage forms and Biological fluids | Prafulla Kumar Sahu (u. a.) | Taschenbuch | 352 S. | Englisch | 2011 | LAP LAMBERT Academic Publishing | EAN 9783844328691 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.
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Analytical Method development by Liquid Chromatography : Development and Validation of Analytical Methods for the Assay of Selected Drugs in Pharmaceutical Dosage forms and Biological fluids
Language: English
Published by LAP LAMBERT Academic Publishing, 2011
ISBN 10: 3844328696 ISBN 13: 9783844328691
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. The current good manufacturing practice (cGMP) and Food Drug Administration (FDA) Guidelines insist for adoption of sound methods of analysis with greater sensitivity and reproducibility. This thesis describes analytical methods developed for drug determination in pharmaceutical dosage forms and biological matrixes including Chromatography (RP-HPLC) and Hyphenated Techniques (LC-MS/MS). Methods have been developed for separation and quantification of selected drugs from categories like Antihypertensive, Antihyperlipidemic, Skeletal Muscle Relaxant, Non-Steroidal Anti-inflammatory Drug (NSAID), Antibiotic, Anticonvulsant, Antiviral, and Analeptic.
