Fabrication of a Selective and Sensitive Sensor Based on Molecularly Imprinted Polymer/Acetylene Black for the Determination of Azithromycin in Pharmaceuticals and Biological Samples
Author(s) -
Tingting Zhou,
Yun Tao,
Hua Jin,
Bin Song,
Tao Jing,
Dan Luo,
Yusun Zhou,
Yikai Zhou,
YongIll Lee,
Surong Mei
Publication year - 2016
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0147002
Subject(s) - molecularly imprinted polymer , differential pulse voltammetry , detection limit , cyclic voltammetry , nip , polymer , carbon paste electrode , chromatography , electrode , carbon black , polymerization , chemistry , analytical chemistry (journal) , materials science , selectivity , organic chemistry , electrochemistry , natural rubber , composite material , catalysis
A new selective and sensitive sensor based on molecularly imprinted polymer/acetylene black (MIP/AB) was developed for the determination of azithromycin (AZM) in pharmaceuticals and biological samples. The MIP of AZM was synthesized by precipitation polymerization. MIP and AB were then respectively introduced as selective and sensitive elements for the preparation of MIP/AB-modified carbon paste (MIP/ABP) electrode. The performance of the obtained sensor was estimated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. Compared with non-molecularly imprinted polymer (NIP) electrodes, NIP/ABP electrodes, and MIP-modified carbon paste electrodes, MIP/ABP electrode exhibited excellent current response toward AZM. The prepared sensor also exhibited good selectivity for AZM in comparison with structurally similar compounds. The effect of electrode composition, extraction parameters, and electrolyte conditions on the current response of the sensor was investigated. Under the optimized conditions, the prepared sensor showed two dynamic linear ranges of 1.0 × 10 −7 mol L −1 to 2.0 × 10 −6 mol L −1 and 2.0 × 10 −6 mol L −1 to 2.0 × 10 −5 mol L −1 , with a limit of detection of 1.1 × 10 −8 mol L −1 . These predominant properties ensured that the sensor exhibits excellent reliability for detecting AZM in pharmaceuticals and biological fluids without the assistance of any separation techniques. The results were validated by the high-performance liquid chromatography–tandem mass spectrometry method.
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