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Evaluation of the effects of atazanavir-ritonavir on the pharmacokinetics of lumefantrine in patients living with HIV in Lagos University Teaching Hospital, South-Western Nigeria.
- Source :
-
European journal of clinical pharmacology [Eur J Clin Pharmacol] 2021 Sep; Vol. 77 (9), pp. 1341-1348. Date of Electronic Publication: 2021 Mar 23. - Publication Year :
- 2021
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Abstract
- Purpose: Atazanavir-ritonavir (ATVr)-based antiretroviral therapy and artemether-lumefantrine (AL) are commonly used drugs for the treatment of human immune deficiency virus (HIV) infection and malaria respectively. However, interaction of both drugs, with Cytochrome P 3A4 (CYP 3A4) isoenzyme, may spawn clinically significant pharmacokinetic interactions. This study evaluated the effects of atazanavir-ritonavir on the pharmacokinetics of lumefantrine.<br />Method: In a case-control study, twenty participants having Plasmodium falciparum malaria were recruited and divided into two groups (ATVr-arm, n=10; and control-arm, n= 10). All the participants were administered six oral doses of AL 80-480 mg (Coartem). Thereafter, their blood samples were collected at different time intervals over seven days. The concentration of lumefantrine in each sample was quantified with high-performance liquid chromatography (HPLC) and used to determine its pharmacokinetic parameters which were compared between the test and control groups.<br />Results: ATVr increased the mean day 7 concentration of lumefantrine (ATVr 3847.09 ± 893.35 ng/mL, control 1374.53 ± 265.55 ng/mL, p = 0.016) and the area under its plasma concentration-time curve (ATVr 670529.57 ± 157172.93 ng.h/mL, control 447976.28 ± 80886.99 ng.h/mL, p = 0.224) by 179.88 % and 49.68 %, respectively, but decreased its mean maximum plasma drug concentration (Cmax) (ATVr 13725.70 ± 2658.44 ng/mL, control 15380.48 ± 2332.62 ng/mL, p = 0.645) by 10.76 %.<br />Conclusion: ATVr increased drug exposure and day 7 plasma concentration of lumefantrine. AL is therefore considered effective for the treatment of malaria in patients taking ATVr-based regimen. However, the safety associated with the interaction requires further elucidation.<br />Trial Registration: Clin ClinicalTrials.gov Identifier: NCT04531072, August 27, 2020. "Retrospectively registered".<br /> (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Subjects :
- Adult
Anti-Retroviral Agents therapeutic use
Antimalarials therapeutic use
Artemether, Lumefantrine Drug Combination therapeutic use
Atazanavir Sulfate therapeutic use
Case-Control Studies
Chromatography, High Pressure Liquid
Drug Combinations
Female
HIV Infections drug therapy
Hospitals, Teaching
Humans
Malaria drug therapy
Male
Middle Aged
Nigeria
Plasmodium falciparum
Racemases and Epimerases
Ritonavir therapeutic use
Anti-Retroviral Agents pharmacology
Antimalarials pharmacokinetics
Artemether, Lumefantrine Drug Combination pharmacokinetics
Atazanavir Sulfate pharmacology
Ritonavir pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1432-1041
- Volume :
- 77
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- European journal of clinical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 33755736
- Full Text :
- https://doi.org/10.1007/s00228-021-03116-x