Chaolong Qin
Development and validation of a cost-effective and sensitive bioanalytical HPLC-UV method for determination of lopinavir in rat and human plasma
Qin, Chaolong; Feng, Wanshan; Chu, Yen Ju; Lee, Jong Bong; Berton, Mattia; Bettonte, Sara; Teo, Yeong Yeu; Stocks, Michael J.; Fischer, Peter M.; Gershkovich, Pavel
Authors
Wanshan Feng
Yen Ju Chu
Jong Bong Lee
Mattia Berton
Sara Bettonte
Yeong Yeu Teo
Professor MICHAEL STOCKS MICHAEL.STOCKS@NOTTINGHAM.AC.UK
PROFESSOR OF MEDICINAL CHEMISTRY AND DRUG DISCOVERY
Peter M. Fischer
Dr PAVEL GERSHKOVICH PAVEL.GERSHKOVICH@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Abstract
© 2020 The Authors. Biomedical Chromatography published by John Wiley & Sons Ltd A simple, sensitive and cost-effective HPLC-UV bioanalytical method for determination of lopinavir (LPV) in rat and human plasma was developed and validated. The plasma sample preparation procedure includes a combination of protein precipitation using cold acetonitrile and liquid–liquid extraction with n-hexane–ethyl acetate (7:3, v/v). A good chromatographic separation was achieved with a Phenomenex Gemini column (C18, 150 mm × 2.0 mm, 5 μm) at 40°C with gradient elution, at 211 nm. Calibration curves were linear in the range 10–10,000 ng/mL, with a lower limit of quantification of 10 ng/mL using 100 μL of plasma. The accuracy and precision in all validation experiments were within the criteria range set by the guidelines of the Food and Drug Administration. This method was successfully applied to a preliminary pharmacokinetic study in rats following an intravenous bolus administration of LPV. Moreover, the method was subsequently fully validated for human plasma, allowing its use in therapeutic drug monitoring (TDM). In conclusion, this novel, simple and cost-efficient bioanalytical method for determination of LPV is useful for pharmacokinetic and drug delivery studies in rats, as well as TDM in human patients.
Citation
Qin, C., Feng, W., Chu, Y. J., Lee, J. B., Berton, M., Bettonte, S., Teo, Y. Y., Stocks, M. J., Fischer, P. M., & Gershkovich, P. (2020). Development and validation of a cost-effective and sensitive bioanalytical HPLC-UV method for determination of lopinavir in rat and human plasma. Biomedical Chromatography, 34(11), Article e4934. https://doi.org/10.1002/bmc.4934
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 24, 2020 |
Online Publication Date | Jul 10, 2020 |
Publication Date | 2020-11 |
Deposit Date | Jul 8, 2020 |
Publicly Available Date | Jul 11, 2021 |
Journal | Biomedical Chromatography |
Print ISSN | 0269-3879 |
Electronic ISSN | 1099-0801 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 34 |
Issue | 11 |
Article Number | e4934 |
DOI | https://doi.org/10.1002/bmc.4934 |
Keywords | Analytical Chemistry; Clinical Biochemistry; Biochemistry; Molecular Biology; Pharmacology; Drug Discovery; General Medicine |
Public URL | https://nottingham-repository.worktribe.com/output/4747375 |
Publisher URL | https://onlinelibrary.wiley.com/doi/abs/10.1002/bmc.4934 |
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Development and validation of a cost‐effective and sensitive bioanalytical HPLC‐UV method for determination of lopinavir in rat and human plasma
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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