Method Development and Quantification of Telmisartan by LC-MS

 
9783659764325: Method Development and Quantification of Telmisartan by LC-MS
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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.

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About the Author:

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.

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Book Description Condition: New. Publisher/Verlag: LAP Lambert Academic Publishing | 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. | Format: Paperback | Language/Sprache: english | 116 pp. Seller Inventory # K9783659764325

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Book Description LAP Lambert Academic Publishing, United States, 2015. Paperback. Condition: New. Language: English . Brand New Book ***** Print on Demand *****.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. Seller Inventory # AAV9783659764325

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Book Description LAP Lambert Academic Publishing Aug 2015, 2015. Taschenbuch. Condition: Neu. 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. Seller Inventory # 9783659764325

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Book Description LAP Lambert Academic Publishing Aug 2015, 2015. Taschenbuch. Condition: Neu. 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. Seller Inventory # 9783659764325

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Book Description LAP Lambert Academic Publishing Aug 2015, 2015. Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand 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. Seller Inventory # 9783659764325

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