Abstract

A simple, rapid and easy method is proposed for the detection of a cytostatic therapeutic drug, cytarabine, in real samples. The method is based on potentiometric transduction using prepared and characterized new ion-selective electrodes for cytarabine. The electrodes were integrated with novel man-tailored imprinted polymers and used as a sensory element for recognition. The electrodes revealed a remarkable potentiometric response for cytarabine over the linearity range 1.0 × 10−6–1.0 × 10−3 M at pH 2.8–4 with a detection limit of 5.5 × 10−7 M. The potentiometric response was near-Nernstian, with average slopes of 52.3 ± 1.2 mV/decade. The effect of lipophilic salts and plasticizer types on the potentiometric response was also examined. The electrodes exhibited an enhanced selectivity towards cytarabine over various foreign common ions. Validation and verification of the presented assay method are demonstrated by evaluating the method ruggedness and calculating the detection limit, range of linearity, accuracy (trueness), precision, repeatability (within-day) and reproducibility (between-days). The proposed ion-selective electrodes revealed good performance characteristics and possible application of these electrodes for cytarabine monitoring in different matrices. The electrodes are successfully applied to cytarabine determination in spiked biological fluid samples and in pharmaceutical formulations.

Highlights

  • Cytarabine, or cytosine arabinoside, is a pyrimidine nucleoside antimetabolite that is cytotoxic to a number of cell types

  • molecularly imprinted polymers (MIPs)-based electrochemical sensors come in various configurations that offer control of electrode

  • MIP-based electrochemical sensors come in various configurations that offer control of properties, such as hydrophobic/hydrophilic character, permeability and film thickness

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Summary

Introduction

Cytarabine, or cytosine arabinoside, is a pyrimidine nucleoside antimetabolite that is cytotoxic to a number of cell types. Polymers 2020, 12, 1343 of cytarabine preparations can be checked using different methods, including titrimetry [4], UV spectrometry [5,6,7], chemiluminescence [8], polarography [9,10,11,12,13,14], voltammetry [15], high performance liquid chromatography (HPLC) [16,17,18,19,20,21,22,23,24,25,26], gas chromatography (GC)/mass spectrometry [27,28,29], micellar electrokinetic capillary chromatography [30,31] and radioimmune assaying [32,33,34,35,36,37,38,39] Most of these methods are considered to have a high cost of use and suffer from limited selectivity and require careful control, whether in reaction conditions or even derivative reactions. With regard to the available literature, no one uses this technique for cytarabine quantification

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