Review of Clinical Pharmacology and Pharmacokinetics – International Edition Volume 38 (2024) – Supplementary Issue 2

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Assessment of antifungal drugs’ activity against some Candida albicans isolates in the presence or absence of human albumin: a study employing an in vitro pharmacokinetics / pharmacodynamics model
Noor Abdalwahd1,2,*Ken (0000-0003-2948-3264) - ORCID, Rafal J. Al-Saigh3Ken (0000-0003-2948-3264) - ORCID, Hussam W. Al-Humadi4Ken (0000-0003-2948-3264) - ORCID
1Department of Pharmacology and Toxicology, College of Pharmacy, University of Babylon, Hillah, Iraq
2Department of Pharmacology, College of Medicine, University of Babylon, Hillah, Iraq
3Department of Clinical Laboratory Sciences, College of Pharmacy, University of Babylon, Hillah, Iraq4College of Pharmacy, University of Babylon, Hillah, Iraq


*Corresponding author:
Noor Abdalwahd, Department of Pharmacology and Toxicology, College of Pharmacy, University of Babylon, Hillah, Iraq; Tel.: +964-(0)7818292905
E-mail: pha416.nour.abdalwahad@uobabylon.edu.iq


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Published: 5 May 2024; https://doi.org/10.61873/SEXH5182

Abstract
Invasive candidiasis associated with the dissemination of endogenous Candida species is a fatal condition linked to high rates of morbidity and mortality. Progressive drug resistance necessitates the need for prompt and effective therapy. Therefore, choosing a specific and effective treatment is crucial. A two-compartment in vitro pharmacokinetics (PK) / pharmacodynamics (PD) model has been used for this purpose, and the PD behaviours of amphotericin B (AMB; at 2.5 and 5 mg/L), voriconazole (VOR; at 1.5 and 3 mg/L), and itraconazole (ITR; at 1.5 and 3 mg/L) were assessed against two Candida albicans isolates (a sensitive and resistant one; ATCC-90028 and ATCC-10231, respectively) with or without the addition of human albumin (2%). PK were simulated as time-concentration profiles, while the PD susceptibility of all drug doses has been assessed through the minimum inhibitory concentration (MIC), the relative optical density of  fungal  growth, and the exposure – effect relationship (fAUC0–24/MIC). A fungicidal activity without the presence of albumin was seen against both isolates of C. albicans at the highest dose of VOR, while the addition of albumin potentiated the efficacies of AMB and of VOR against both isolates, with no effect for ITR. Finally, human albumin exerted a variable and dose-dependent effect on the activities of some antifungal agents.

Keywords: antifungal drugs, Candida species, in vitro model, pharmacokinetics, pharmacodynamics

Please cite as:
Abdalwahd N., Al-Saigh R.J., Al-Humadi H.W. Assessment of antifungal drugs’ activity against some Candida albicans isolates in the presence or absence of human albumin: a study employing an in vitro pharmacokinetics / pharmacodynamics model. Rev. Clin. Pharmacol. Pharmacokinet. Int. Ed. 38(Sup2): 39-42 (2024). https://doi.org/10.61873/SEXH5182

 

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