Method Development Quantification Telmisartan by Khurana Lakshika (5 results)

Taschenbuch. Condition: Neu. Method Development and Quantification of Telmisartan by LC-MS | Lakshika Khurana (u. a.) | Taschenbuch | 116 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659764325 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. …

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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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.LC-PDA 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. 116 pp. Englisch.…

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Khurana LakshikaMs 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.…

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -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.LC¿PDA 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.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 116 pp. Englisch.…