UV AND HPLC Method Development and Method Validation of Nevirapine
UV AND HPLC Method Development and Validation of Nevirapine in Bulk and Pharmaceutical dosage forms
(Sprache: Englisch)
This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A...
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This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms.
Autoren-Porträt von Tirthankar Choudhury
Choudhury, TirthankarDr. (Prof.) Tirthankar Choudhury had his M. Pharm (Pharm. Chemistry) in 2008 and Ph.D.(Pharmaceutical Science) in 2012. Till now he had 11 years of teaching experience along with several paper publications. Now he is associated with Editorial and Advisory Boards of many journals.Hoping towards his wide acceptance in Pharmacy profession.
Bibliographische Angaben
- Autor: Tirthankar Choudhury
- 2019, 108 Seiten, Maße: 22 cm, Kartoniert (TB), Englisch
- Verlag: LAP Lambert Academic Publishing
- ISBN-10: 6200218099
- ISBN-13: 9786200218094
Sprache:
Englisch
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