Development a validated highly sensitive LC–MS/MS method for simultaneous quantification of Ledipasvir, sofosbuvir and its major metabolite GS-331007 in human plasma: Application to a human pharmacokinetic study-Reference-Cited by-同舟云学术

Development a validated highly sensitive LC–MS/MS method for simultaneous quantification of Ledipasvir, sofosbuvir and its major metabolite GS-331007 in human plasma: Application to a human pharmacokinetic study

Published:2017-09 Issue: Volume:143 Page:305-310
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Abdallah Ola M.,Abdel-Megied Ahmed M.,Gouda Amira S.

Publisher

Elsevier BV

Subject

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

Reference19 articles.

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2. Sofosbuvir: a novel oral agent for chronic hepatitis C;Cholongitas;Ann. Gastroenterol.,2014

3. Treatment of hepatitis C: a systematic review;Kohli;JAMA,2014

4. Ledipasvir and sofosbuvir for previously treated HCV genotype 1 infection;Afdhal;N. Engl. J. Med.,2014

5. Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection;Afdhal;N. Engl. J. Med.,2014

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