Electrochemical Detection of Epicatechin in Green Tea Using Quercetin-Imprinted Polymer Graphite Electrode

被引:15
作者
Das, Debangana [1 ]
Nag, Shreya [1 ]
De, Shubham [1 ]
Hazarika, Ajanto Kumar [2 ]
Sabhapondit, Santanu [2 ]
Tudu, Bipan [1 ]
Bandyopadhyay, Rajib [1 ]
Pramanik, Panchanan [3 ]
Roy, Runu Banerjee [1 ]
机构
[1] Jadavpur Univ, Dept Instrumentat & Elect Engn IEE, Kolkata 700106, India
[2] Tocklai Tea Res Inst, Jorhat 785008, Assam, India
[3] GLA Univ, Dept Chem & Nanosci, Mathura 281406, India
关键词
Quercetin; MIP; green tea; epicatechin; regression models; CATECHIN; VOLTAMMETRY; ACID;
D O I
10.1109/JSEN.2021.3122145
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The current study utilizes molecularly imprinted polymer (MIP) technology to fabricate a cost-effective and reproducible electrode for selective determination and quantitative prediction of epicatechin (EC) in green tea. Acrylamide (AAm) co-polymerized with ethylene glycol dimethacrylate (EGDMA) and optically inactive quercetin (Q) as the template has been used to make the MIP-Q@G material. The voltammetric experiment has been performed using the MIP-Q@G electrode with the help of a three-electrode configuration. In addition to a low detection limit (LoD) of 0.33 mu M , the electrode exhibited two wide ranges of linearity from 1 mu M - 100 mu M and 100 mu M to 500 mu M . The limit of quantitation (LoQ) of the electrode was found to be 1.09 mu M . Partial least square regression (PLSR) and principal component regression (PCR) models have been developed to investigate the predictive ability of the MIP-Q@G electrode using the differential pulse voltammetry (DPV) signals and the high- performance liquid chromatography (HPLC) data. Both PLSR and PCR models achieved prediction accuracies of 94.54 % and 94.41% with a root mean square error of calibration (RMSEC) of 0.113 and 0.119, respectively.
引用
收藏
页码:26526 / 26533
页数:8
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