ESI-MSn and LC–ESI-MS studies to characterize forced degradation products of bosentan and a validated stability-indicating LC

ESI-MSn and LC–ESI-MS studies to characterize forced degradation products of bosentan and a validated stability-indicating LC–UV method

Published:2013-01 Issue: Volume:72 Page:186-197
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Bansal Gulshan,Singh Ranjit,Saini Balraj,Bansal Yogita

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference17 articles.

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3. http://clinicaltrials.gov/show/NCT00367770 (accessed 11/9/2011).

4. Determination of an endothelin receptor antagonist in human plasma by narrow-bore liquid chromatography and ion spray tandem mass spectrometry;Lausecker;J. Chromatogr. A,1995

5. Determination of tezosentan, a parenteral endothelin receptor antagonist, in human plasma by liquid chromatography–tandem mass spectrometry;Paul;J. Chromatogr. B,2003

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