Neurotransmitter Biomolecule Transfers Across Liquid/Liquid Interface Through A Thick Organic Membrane-Modified Electrode

被引:0
作者
Zhong Li-Jie [1 ]
Gao Li-Fang [2 ,3 ]
Li Feng-Hua [2 ]
Gan Shi-Yu [1 ,2 ]
Niu Li [1 ,2 ]
机构
[1] Guangzhou Univ, Sch Chem & Chem Engn, Ctr Adv Analyt Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Engn Lab Modern Analyt Tech, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Neurotransmitter; Liquid/liquid interfaces; Electron and ion transfers; Voltammetry; Membrane; FILM-MODIFIED ELECTRODE; BAR-LIQUID INTERFACE; ION-TRANSFER; ANION TRANSFER; WATER/NITROBENZENE INTERFACE; WATER-NITROBENZENE; AMINO-ACIDS; VOLTAMMETRY; KINETICS; ELECTROCHEMISTRY;
D O I
10.1016/S1872-2040(18)61137-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrochemical studies at liquid/liquid interfaces (L/L, or soft interfaces) have disclosed a biomimetic model to mimic charge transfers at cytomembrane surface. Herein, we reported two neurotransmitter biomolecules of dopamine and adrenalone across the L/L interface by a thick organic membrane-modified electrode. This system comprised polarized electrode/oil and oil/water interfaces in series in which the electron transfer (ET) of redox 7,7,8,8-tetracyanoquinodimethane (TCNQ) at electrode/oil interface drove ion transfer (IT) of biomolecules at oil/water interface. This ET-IT coupled reaction overcame the limitation of polarized potential window at conventional single polarized L/L interface. The crucial design of a thick organic membrane could ensure the generated TCNQ anions maintained at electrode/oil interface during the voltammetry, which could not result in interruptions to biomolecule transfers. Through this system, their Gibbs transfer free energies were accurately determined (44.4 and 39.4 kJ mol(-1) for dopamine and adrealone, respectively). Moreover, facilitated biomolecule transfers were evaluated by crown ionophores where both facilitated numbers and constants were determined simultaneously. Owing to the simple electrochemical setup, this system would hold great potentials in future hydrophilic biomacromolecule transfers, such as DNA, peptides and proteins.
引用
收藏
页码:E19001 / E19008
页数:8
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