电化学生物传感器 2010

Enhanced electrochemical oxygen reduction-based glucose sensing using glucose oxidase on nanodendritic poly[meso-tetrakis(2-thienyl)porphyrinato]cobalt(II)-SWNTs composite electrodes.

Biosensors & bioelectronics Chen W, Ding Y, Akhigbe J, Brückner C, Li CM, Lei Y
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组成图示

Enhanced electrochemical oxygen reduc... 传感器构成示意图

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传感器类型

电化学生物传感器

检测对象

葡萄糖(glucose,β-D-glucose);样品基质:0.01 M PBS缓冲液(pH 7.4),文中讨论血清中尿酸/抗坏血酸干扰。

检测原理

葡萄糖氧化酶(GOD)固定于pCoTTP-SWNTs-Nafion复合膜中,催化β-D-葡萄糖氧化为葡萄糖酸内酯,FAD/FADH2发生两电子两质子转移,分子氧作为最终电子受体被还原为过氧化氢,从而消耗溶解氧。pCoTTP纳米树枝状膜与SWNTs协同降低氧还原过电位,使氧还原峰电位降至约−0.2 V vs. Ag/AgCl。在恒定−0.2 V下,溶解氧在电极界面发生电催化还原产生还原电流;葡萄糖浓度升高时,GOD消耗O2增多,氧还原电流下降,形成负向安培响应。Nafion固定酶并排斥阴离子,提高选择性。

检测灵敏度

LOD: 5.33 μM (S/N = 3);线性范围: 0–1 mM(原文 up to 1 mM);灵敏度: 16.57 μA mM−1 cm−2;R^2 = 0.998

效应效果

传感器在−0.2 V下对葡萄糖快速响应,15 s内达到稳态;线性范围达1 mM,LOD 5.33 μM,灵敏度16.57 μA mM−1 cm−2,R^2=0.998,Km,app 0.98 mM,优于或接近文献值1.1 mM和2.4 mM。0.2 mM尿酸和抗坏血酸均不干扰,归因于低电位和Nafion阴离子排斥。GOD电子转移速率ks为1.01 s−1,高于0.3 s−1和0.026 s−1的文献值。作者认为该pCoTTP-SWNTs-Nafion-GOD/GCE可用于高灵敏、高选择性葡萄糖检测,但未报告稳定性、RSD和实际样品回收率。

传感器的构成

  • 基底/换能器电极:玻碳电极(GCE,3 mm),经Al2O3抛光,提供导电基底与电子转移动力。
  • 纳米催化修饰层:纳米树枝状聚[meso-四(2-噻吩基)卟啉]钴(II)(pCoTTP)电聚合膜,降低氧还原过电位并增强电子转移。
  • 导电/多孔复合层:单壁碳纳米管(SWNTs)与Nafion复合膜,提供导电通道、多孔结构和GOD负载界面。
  • 识别元件:葡萄糖氧化酶(GOD),催化葡萄糖氧化并消耗溶解氧。
  • 固定/封闭层:Nafion(20 wt%乙醇溶液,最终约0.5 wt%),固定SWNTs-GOD并排斥阴离子干扰。
  • 信号介质:溶解氧(O2),在低电位下被电催化还原,葡萄糖消耗O2导致还原电流下降。
  • 缓冲介质:0.01 M磷酸盐缓冲液(PBS,pH 7.4),维持酶活性与电化学环境。

中文摘要

报道了固定化在纳米树枝状聚[meso-四(2-噻吩基)卟啉]钴(II)-单壁碳纳米管修饰玻碳电极(pCoTTP-SWNTs-Nafion-GOD/GCE)上的葡萄糖氧化酶(GOD)的直接电化学行为。固定化GOD保持活性,呈现表面控制的可逆两质子两电子转移反应,异相电子转移速率常数ks为1.01 s−1。pCoTTP-SWNTs-Nafion基质对氧还原表现出极低峰电位(−0.2 V vs. Ag/AgCl)和强响应,为基于氧还原的葡萄糖检测平台奠定基础。表观米氏常数Km,app低至0.98 mM。葡萄糖线性范围达1 mM,检出限5.33 μM(S/N=3),灵敏度16.57 μA mM−1 cm−2。对0.2 mM尿酸和抗坏血酸具有优异选择性。结果表明该传感器在灵敏、选择性葡萄糖检测中具有应用潜力。

英文摘要

The direct electrochemistry of glucose oxidase immobilized on a nanodendritic poly[meso-tetrakis(2-thienyl)porphyrinato]cobalt(II)-single walled carbon nanotube modified glassy carbon electrode (pCoTTP-SWNTs-Nafion-GOD/GCE) is reported. The immobilized GOD retained its activity and exhibited a surface controlled, reversible two-proton and two-electron transfer reaction with a fast heterogeneous electron transfer rate constant (ks) of 1.01 s(-1). The pCoTTP-SWNTs-Nafion matrix also showed an extremely low peak potential of -0.2 V vs. Ag/AgCl and strong response with respect to oxygen reduction. This forms the basis for the use of the pCoTTP-SWNTs-Nafion-GOD composite as a sensing platform for oxygen reduction-based glucose detection. The apparent Michaelis-Menten constant (Km,app) was estimated to be as low as 0.98 mM. A linear range up to 1mM glucose with a low detection limit of 5.33 μM (S/N=3) and a high sensitivity of 16.57 μA mM(-1) cm(-2) was achieved. The biosensor also shows excellent selectivity against 0.2 mM uric acid and ascorbic acid. These results indicate that the pCoTTP-SWNTs-Nafion-GOD/GCE has potential application in sensitive and selective glucose detection.