Abstract
A simple and efficient new electrochemical sensor based on molecularly imprinted polymer has been developed for selective detection of an anticancer agent Etoposide (ETP). The sensor was prepared by electropolymerization via cyclic voltammetry (CV) of pyrrole onto a glassy carbon electrode (GCE) in the presence of ETP molecules. The extraction of ETP molecules embedded in the polymeric matrix was carried out by overoxidation in sodium hydroxide medium using CV. Various important parameters affecting the performance of the imprinted film (MIP) coated sensor were studied and optimized using differential pulse voltammetry (DPV). Under optimal conditions, the sensor response exhibited a linear dependence on ETP concentration (R2= 0.999) over the range 5.0×10−7M – 1.0×10−5M with a LOD (3σ/m) of 2.8×10−9M. The precision (% RSD, n=6) of the proposed sensor for intra- and interdays was found to be 0.84 and 2.46%, respectively. The selectivity of MIP/GCE sensor toward ETP was investigated in the presence of different interfering molecules including excipients and ETP metabolites. The developed sensor showed great recognition ability toward ETP and was successfully applied for its determination in injectable dosage forms and biological human fluids.
Highlights
Etoposide (ETP) (4-demethylepipodophyllotoxin ethylidene- b-D-glucoside) is a potent clinical anticancer agent [1]
The voltammograms corresponding to molecularly imprinted polymers (MIP) and nonimprinted electrode (NIP) formation look similar in shape, an anodic peak corresponding to the oxidation of ETP and appearing at about 0.6 V was exclusively recorded with MIP film
The obvious increase of anodic and cathodic current intensities of MIP film in comparison with NIP film reveals the difference of MIP and NIP growth
Summary
Etoposide (ETP) (4-demethylepipodophyllotoxin ethylidene- b-D-glucoside) is a potent clinical anticancer agent [1]. Literature research indicated various studies describing several analytical methods for the determination of ETP in many matrices including injectable dosage forms, biological fluids, and cancer cells. These methods are almost based on high-performance liquid chromatography [10,11,12,13,14,15,16,17,18,19], spectrofluorimetry [20], and micellar electrokinetic chromatography [21]. To the best of our knowledge, the proposed method is the first application of MIP modified electrochemical sensor for ETP determination
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