Development of a Cr2AlC MAX phase/g-C3N4 composite-based electrochemical sensor for accurate cabotegravir determination in pharmaceutical and biological samples
- PMID: 38355771
- DOI: 10.1007/s00604-024-06207-5
Development of a Cr2AlC MAX phase/g-C3N4 composite-based electrochemical sensor for accurate cabotegravir determination in pharmaceutical and biological samples
Abstract
A highly sensitive electrochemical sensor is reported that employs a modified electrode for the precise measurement of cabotegravir, a potent anti-HIV drug. Cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS) were utilized for this purpose. Electrode modification involved the immobilization of Cr2AlC MAX phase/g-C3N4 onto a glassy carbon electrode (GCE) to enhance its electrocatalytic activity and selectivity for cabotegravir detection. Under the optimal experimental conditions, the working potential (vs. Ag/AgCl) was to 0.93 V. The developed sensor exhibited a good linear relationship in the range 0.05 µM to 9.34 µM with a low limit of detection of 4.33 nM, signifying its exceptional sensitivity. Additionally, it demonstrated successful cabotegravir detection in pharmaceutical formulations and biological samples, achieving an RSD below 3.0%. The recoveries fell within the range 97.7 to 102%, confirming the sensor's potential for real-sample applications. This innovative electrochemical sensor represents a significant advancement, providing a simple, reliable, and sensitive tool for the accurate measurement of cabotegravir. Its potential applications include optimizing drug dosages, monitoring treatment responses, and supporting the development of cabotegravir-based pharmaceutical products, thereby contributing to advancements in HIV therapy and prevention strategies.
Keywords: Cabotegravir; Cr2AlC MAX phase; Differential pulse voltammetry; Electrochemical sensor; Modified glassy carbon electrode; Pharmaceutical products; g-C3N4.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.
References
-
- Han Y, Mesplède T, Wainberg M (2015) Cabotegravir. HIV integrase inhibitor, anti-HIV agent. Drugs Future 40(11). https://doi.org/10.1358/dof.2015.040.11.2383040
-
- Taki E, Soleimani F, Asadi A et al (2022) Cabotegravir/Rilpivirine: the last FDA-approved drug to treat HIV. Expert Rev Anti Infect Ther 20:1135–1147. https://doi.org/10.1080/14787210.2022.2081153 - DOI - PubMed
-
- Prasanna A, Rani SS (2022) A Validated Stability Indicating RP-HPLC Method Development for Simultaneous estimation of Cabotegravir and Rilpivirine in Pharmaceutical Dosage form. World J Pharm Sci 22–29. https://doi.org/10.54037/WJPS.2022.101003
-
- Blair HA (2022) Cabotegravir extended-release injectable suspension: A review in HIV-1 pre-exposure prophylaxis. Drugs 82:1489–1498. https://doi.org/10.1007/s40265-022-01791-3 - DOI - PubMed
-
- Enggi CK, Isa HT, Wijaya S et al (2022) Validation of spectrophotometric method to quantify cabotegravir in simulated vaginal fluid and porcine vaginal tissue in ex vivo permeation and retention studies from thermosensitive and mucoadhesive gels. Spectrochim Acta Part A Mol Biomol Spectrosc 267:120600. https://doi.org/10.1016/j.saa.2021.120600 - DOI