Issue 70, 2020, Issue in Progress

Portable solid-state sensor for therapeutic monitoring of an antineoplastic drug; vinblastine in human plasma

Abstract

During cancer treatment, doses must be carefully administered and monitored to guarantee efficacy and minimize side-effects. A potentiometric sensor was developed for the direct real-time assay of a widely used antineoplastic drug (vinblastine (VB)) in plasma samples. Membrane cocktails were drop-casted over a glassy-carbon electrode coated with a lipophilic conducting polymer (polyaniline). The study investigated five cation exchangers, five plasticizers (of different polarities and dielectric constants), and four ionophores with different physicochemical characters on the sensor performance. The study substantiates a data-driven selection of the optimum membrane recipe. The latter included sodium tetraphenylborate as an ion exchanger, dioctylphthalate as a plasticizer, and hydroxypropyl-β-cyclodextrin as ionophore. The membrane proved a near-Nernstian slope of 37.5 mV per decade, a LOQ of 2.99 × 10−6 M, and a stable fast response. The selectivity study proved poor responses to common physiological ions. The developed sensor was used for the determination of VB in its pure powder form, marketed formulation, and plasma samples. The fast and direct sensor response enables a wide range of applications in quality control laboratories and clinical studies.

Graphical abstract: Portable solid-state sensor for therapeutic monitoring of an antineoplastic drug; vinblastine in human plasma

Supplementary files

Article information

Article type
Paper
Submitted
17 Aug 2020
Accepted
14 Nov 2020
First published
24 Nov 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 42699-42705

Portable solid-state sensor for therapeutic monitoring of an antineoplastic drug; vinblastine in human plasma

M. M. Galal and A. S. Saad, RSC Adv., 2020, 10, 42699 DOI: 10.1039/D0RA07070J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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