Detailansicht
Method Development and Quantification of Telmisartan by LC-MS
ISBN/EAN: 9783659764325
Umbreit-Nr.: 8562489
Sprache:
Englisch
Umfang: 116 S.
Format in cm: 0.7 x 22 x 15
Einband:
kartoniertes Buch
Erschienen am 21.08.2015
Auflage: 1/2015
€ 54,90
(inklusive MwSt.)
Lieferbar innerhalb 1 - 2 Wochen
- Zusatztext
- Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability and to provide information about degradation pathways and degradation products.The impurity profiling of the pharmaceuticals is of increasing importance as drug safety receives more and more attention from the public and from the media.LCPDA method enables simple, accurate, reproducible and fast quantitative analysis of telmisartan in presence of degradation products. The method has been successfully applied to stability study. For quantification the training has helped in learning to develop a new, rapid, sensitive and precise MRM LC-ESI-MS-MS method for the simultaneous separation and quantification pharmaceutical drug telmisartan and its marketed formulation. The HPTLC method is sensitive, precise and accurate and can be used for the routine quality control analysis of telmisartan in its tablet dosage forms.
- Autorenportrait
- Ms Lakshika Khurana from Alwar College of Pharmacy, an ardent scholar and faculty in Pharmaceutics. She is active member of various professional bodies and presented many papers in national and international seminars. He has published lot of scientific work at national and international repute journals.
