Development and validation of a UPLC–MS/MS method for the simultaneous determination of paritaprevir and ritonavir in rat liver

Author:

Ocque Andrew J1,Hagler Colleen E1,Difrancesco Robin1,Woolwine-Cunningham Yvonne2,Bednasz Cindy J1,Morse Gene D1,Talal Andrew H3

Affiliation:

1. Translational Pharmacology Research Core, Department of Pharmacy Practice, School of Pharmacy & Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics & Life Sciences, University at Buffalo, Buffalo, NY, USA

2. Clinical & Translational Research Center, University at Buffalo, Buffalo, NY, USA

3. Division of Gastroenterology & Hepatology & Center for Clinical & Research in Liver Disease, Jacobs School of Medicine, University at Buffalo, Buffalo, NY, USA

Abstract

Aim: Determination of paritaprevir and ritonavir in rat liver tissue samples. Results: We successfully validated a UPLC–MS/MS method to measure paritaprevir and ritonavir in rat liver using deuterated internal standards (d8-paritapervir and d6-ritonavir). The method is linear from 20 to 20,000 and 5 to 10,000 pg on column for paritaprevir and ritonavir, respectively, and is normalized per milligram tissue. Interday and intraday variability ranged from 0.591 to 5.33% and accuracy ranged from -6.68 to 10.1% for quality control samples. The method was then applied to the measurement of paritaprevir and ritonavir in rat liver tissue samples from a pilot study. Conclusion: The validated method is suitable for measurement of paritaprevir and ritonavir within rat liver tissue samples for PK studies.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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