Development and Validation of a Rapid and Sensitive Assay for Simultaneous Quantification of Lenalidomide and Dexamethasone in Human Plasma by Liquid Chromatography Coupled to Tandem Mass-Spectrometry-Reference-Cited by-同舟云学术

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Development and Validation of a Rapid and Sensitive Assay for Simultaneous Quantification of Lenalidomide and Dexamethasone in Human Plasma by Liquid Chromatography Coupled to Tandem Mass-Spectrometry

Published:2011-11-01 Issue:4 Volume:7 Page:240-247
ISSN:1573-4129
Container-title:Current Pharmaceutical Analysis
language:en
Short-container-title:CPA

Author:

Gopinath Shanmugam,S. Kumar Ramadass,Alexander Sekar,Danabal Palanisamy

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science,Molecular Medicine,Biochemistry,Biophysics

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Review: Method Development Validation and Degradation Studies of some Anticancer Drugs;Research Journal of Pharmacy and Technology;2021-10-31

2. Development and validation of a liquid chromatography-tandem mass spectrometric method for the determination of lenalidomide in human plasma and its application on bioequivalence studies;Journal of Analytical Science and Technology;2019-11-28

3. Improved UV Spectrophotometric Method for Precise, Efficient and Selective Determination of Dexamethasone in Pharmaceutical Dosage Forms;Orbital - The Electronic Journal of Chemistry;2015-04-05

4. A New Facilitated Solid Phase Extraction Method for Bioavailability Evaluation of Lisinopril in Fasting Healthy Male Volunteers;Current Pharmaceutical Analysis;2012-10-01

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