Method Validation and Stability Analysis of Rifampicin by LC and LC-MS | Stability Studies of Rifampicin: Method Validation, and Characterization of Degradation Products by LC and LC-MS.

Trupesh Pethani (u. a.)

ISBN 10: 6202433051 / ISBN 13: 9786202433051

Published by LAP LAMBERT Academic Publishing, 2025

About this Item

Method Validation and Stability Analysis of Rifampicin by LC and LC-MS | Stability Studies of Rifampicin: Method Validation, and Characterization of Degradation Products by LC and LC-MS. | Trupesh Pethani (u. a.) | Taschenbuch | Englisch | 2025 | LAP LAMBERT Academic Publishing | EAN 9786202433051 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.

Seller Inventory # 134120160

Bibliographic Details

• Title: Method Validation and Stability Analysis of Rifampicin by LC and LC-MS | Stability Studies of Rifampicin: Method Validation, and Characterization of Degradation Products by LC and LC-MS.
• Publisher: LAP LAMBERT Academic Publishing
• Publication Date: 2025
• Language: English
• ISBN 10: 6202433051
• ISBN 13: 9786202433051
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 220W x 150H x 7D millimeters 220 millimeters width by 150 millimeters height by 7 millimeters depth
• Weight: 173 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

This book presents a comprehensive study on the stability of rifampicin, a first-line anti-tuberculosis drug, through method development, validation, and characterization of its degradation products. It begins with an overview of tuberculosis, rifampicin's pharmacological profile, and the importance of stability-indicating methods in pharmaceutical quality control. Using HPLC and LC-MS techniques, the study optimizes chromatographic conditions and develops a validated stability-indicating method as per ICH guidelines. Forced degradation experiments under acidic, alkaline, oxidative, photolytic, and thermal stress reveal rifampicin's susceptibility to hydrolysis and other degradative pathways, with detailed characterization of degradation products. The validated method demonstrated accuracy, precision, linearity, robustness, and suitability for analyzing rifampicin in bulk and dosage forms. The work highlights the scientific and regulatory significance of stability testing in ensuring drug safety, efficacy, and quality throughout its shelf life, offering valuable insights for pharmaceutical research and development.