Novel determination of sofosbuvir and velpatasvir in human plasma by UPLC-MS/MS method: Application to a bioequivalence study-Reference-Cited by-同舟云学术

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Novel determination of sofosbuvir and velpatasvir in human plasma by UPLC-MS/MS method: Application to a bioequivalence study

Published:2018-08-23 Issue:11 Volume:32 Page:e4347
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Rezk Mamdouh R.¹^ORCID,Basalious Emad B.²,Badr Kamal A.³⁴

Affiliation:

1. Analytical Chemistry Department, Faculty of Pharmacy; Cairo University; Cairo Egypt

2. Pharmaceutics and Industrial Pharmacy Department, Faculty of Pharmacy; Cairo University; Cairo Egypt

3. Pharmaceutics Department, Faculty of Pharmacy; Deraya University; Egypt

4. Advanced Research Center, Nasr City; Cairo Egypt

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bmc.4347/fullpdf

Reference18 articles.

1. Ledipasvir and sofosbuvir for previously treated HCV genotype 1 infection;Afdhal;The New England Journal of Medicine,2014

2. UHPLC-MS/MS method for the quantification of direct antiviral agents simeprevir, daclatasvir, ledipasvir, sofosbuvir/GS-331007, dasabuvir, ombitasvir and paritaprevir, together with ritonavir, in human plasma;Ariaudo;Journal of Pharmaceutical and Biomedical Analysis,2016

3. Sofosbuvir and velpatasvir for HCV in patients with decompensated cirrhosis;Curry;The New England Journal of Medicine,2015

4. Matrix effect in bio-analysis of illicit drugs with LC-MS/MS: Influence of ionization type, sample preparation, and biofluid;Dams;Journal of the American Society for Mass Spectrometry,2003

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