Validation & Stability Indicating RP-HPLC Method for Meloxicam Capsule | Developed and Validated as per ICH guidelines

Adil Wali (u. a.)

ISBN 10: 3659756865 / ISBN 13: 9783659756863

Published by LAP LAMBERT Academic Publishing, 2015

About this Item

Validation & Stability Indicating RP-HPLC Method for Meloxicam Capsule | Developed and Validated as per ICH guidelines | Adil Wali (u. a.) | Taschenbuch | 144 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659756863 | Verantwortliche Person für die EU: OmniScriptum GmbH & Co. KG, Bahnhofstr. 28, 66111 Saarbrücken, info[at]akademikerverlag[dot]de | Anbieter: preigu.

Seller Inventory # 104305578

Bibliographic Details

• Title: Validation & Stability Indicating RP-HPLC Method for Meloxicam Capsule | Developed and Validated as per ICH guidelines
• Publisher: LAP LAMBERT Academic Publishing
• Publication Date: 2015
• Language: English
• ISBN 10: 3659756865
• ISBN 13: 9783659756863
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 220W x 150H x 10D millimeters 220 millimeters width by 150 millimeters height by 10 millimeters depth
• Weight: 233 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

Meloxicam (4-hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3carboxamide-1,1 -dioxide) is an NSAID used in the management of rheumatic disease, which is distinguished by the fact that it is well tolerated by the stomach at the doses necessary for therapy. The anti-inflammatory and pain-relieving properties of Meloxicam make this active substance very interesting for use in pain therapy. Meloxicam act as nonselective inhibitor of the enzyme cyclooxygenase (COX), inhibiting both the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) isoenzymes. A rapid, specific isocratic RP-HPLC method has been developed for the determination of Meloxicam capsules using a UV/diode array detector. The method was validated as per ICH guidelines and USP/NF. Therefore, this method can be useful for routine analysis of Meloxicam capsules as bulk drug and dosage form.

About the Author

The author has been working in the field of Pharmaceutical Chemistry since 2009. He has worked in pharmaceutical industry in the field of Analytical Research and Development and had been actively engaged in the quality control of drugs using modern analytical techniques like LCMS/MS, UHPLC, HPLC, HPTLC, NMR and Mass Spectrometry.