Impurity Profiling of Drugs and Pharmaceuticals | New Analytical Methods- Development and Validation

M V Narendra Kumar Talluri

ISBN 10: 3843388024 / ISBN 13: 9783843388023

Published by LAP LAMBERT Academic Publishing, 2011

About this Item

Impurity Profiling of Drugs and Pharmaceuticals | New Analytical Methods- Development and Validation | M V Narendra Kumar Talluri | Taschenbuch | 176 S. | Englisch | 2011 | LAP LAMBERT Academic Publishing | EAN 9783843388023 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.

Seller Inventory # 107124269

Bibliographic Details

• Title: Impurity Profiling of Drugs and Pharmaceuticals | New Analytical Methods- Development and Validation
• Publisher: LAP LAMBERT Academic Publishing
• Publication Date: 2011
• Language: English
• ISBN 10: 3843388024
• ISBN 13: 9783843388023
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 220W x 150H x 11D millimeters 220 millimeters width by 150 millimeters height by 11 millimeters depth
• Weight: 280 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

Drug Impurity Profiling: The need to develop new analytical methods for assurance of quality, safety and efficacy of drugs and pharmaceuticals is quite important because of their use not only as health care products but also life saving substances. The analytical methods assume of great importance due to i) development of new drugs ii) continuous changes in manufacturing processes for existing drugs and iii) setting up of threshold limits for individual and total impurities of drugs by regulatory authorities. Keeping this in view, an attempt was made in the present investigation to develop new analytical methods for some of the important drugs and pharmaceuticals of ?1-adrenergic receptor antagonist, antidepressants, cardiovascular agents, antioxidants and tuberculostatics in nature. All the methods described in the book are simple, rapid, reliable and validated. The methods could be used not only for quality control but also for process development of bulk drugs. The work carried out in the present investigation was described in six chapters.

About the Author

Dr. M.V. Narendra. K. Talluri, Ph.D. is a Faculty, Pharmaceutical Analysis at NIPER, Hyderabad. Previous position held by him- Asso. Scientific Manager at BMS.Received PhD degree from IICT. Published 15 research, book chapter and reviews in reputed journals. Recipient of AIC award-Institution of Chemists and Research fellowship of CSIR.