Tyramine detection using PEDOT:PSS/AuNPs/1-methy1-4-mercaptopyridine modified screen-printed carbon electrode with molecularly imprinted polymer solid phase extraction

被引:35
作者
Li, Ying [1 ]
Hsieh, Cheng-Hung [2 ]
Lai, Chi-Wei [2 ]
Chang, Ying-Feng [1 ]
Chan, Hsin-Yi [2 ]
Tsai, Chang-Feng [2 ]
Ho, Ja-An Annie [1 ]
Wu, Li-Chen [2 ]
机构
[1] Natl Taiwan Univ, Dept Biochem Sci & Technol, BioAnalyt Chem & Nanobiomed Lab, Taipei 10617, Taiwan
[2] Natl Chi Nan Univ, Dept Appl Chem, Nantou 545, Taiwan
关键词
Tyramine; Electrochemical analysis; 1-Methyl-4-pyridine; PEDOT: PSS; Gold nanoparticles; TANDEM MASS-SPECTROMETRY; BIOGENIC-AMINES; ELECTROCHEMICAL SENSOR; MONOAMINE-OXIDASE; PRESSOR-RESPONSE; CHROMATOGRAPHY; LIQUID; PRECONCENTRATION; VOLTAMMETRY; RECOGNITION;
D O I
10.1016/j.bios.2016.08.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Tyramine (4-hydroxyphenethylamine), which is a monoamine metabolized by monoamine oxidase (MAO), exists widely in plants, animals, fermented foods, and salted foods. The incidence of hypertension, or "cheese effect", which is associated with a large dietary intake of tyramine while taking MAO inhibitors has been reported; therefore, the measurement of tyramine is an urgent concern. Herein, an efficient approach that integrates a molecular imprinting polymer for solid phase extraction (MISPE) technique with a sensitive electrochemical sensing platform (SPCE/PEDOT: PSS/AuNP/1-m-4-MP) for the quantification of tyramine is presented. Enhanced electrode conductivity was achieved sequentially by constructing a conductive polymer (PEDOT: PSS) on a screen-printed carbon electrode (SPCE), followed by electrodeposition with gold nanoparticles (AuNPs) and, finally, by modification with positively charged 1-methyl-4-mercaptopyridine (1-m-4-MP) using an Au-S bond. Tyramine was isolated selectively and pre-concentrated by the MISPE technique; electroanalysis that used differential pulse voltammetry (DPV) in NaOH (0.1 M, pH 13) was conducted successively. Experimental parameters (such as modes of electrode modification, ratio of PEDOT: PSS, pH of electrolyte, time required for AuNP deposition, and 1-m-4-MP concentrations) that were associated with optimal detection conditions were evaluated also. We obtained a linear concentration range (5-100 nM, R-2=0.9939) with LOD and sensitivity at 2.31 nM, and 3.11 mu A nM(-1) cm(-2), respectively. The applicability of our technique was demonstrated by analyzing tyramine in spiked serum and milk. The feature of our newly developed analytical methods that coupled sample pre-treatment (sample clean-up and pre-concentration) with sensitive detection makes it a promising tool for quantifying of tyramine. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 149
页数:8
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