电化学生物传感器 2011

[C3(OH)2mim][BF4]-Au/Pt biosensor for glutamate sensing in vivo integrated with on-line microdialysis system.

Biosensors & bioelectronics Yu Y, Liu X, Jiang D, Sun Q, Zhou T, Zhu M, Jin L, Shi G
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组成图示

[C3(OH)2mim][BF4]-Au/Pt biosensor for... 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

谷氨酸(glutamate, Glu);样品基质:大鼠纹状体脑微透析液(in vivo)及人工脑脊液(aCSF)标准液(in vitro)

检测原理

谷氨酸在谷氨酸氧化酶(GlutaOx)催化下与O2反应被氧化,生成H2O2。H2O2扩散至[C3(OH)2mim][BF4]膜中的Au/Pt纳米粒子表面,在-200 mV工作电位下发生电催化还原,产生与谷氨酸浓度成正比的阴极电流。羟基官能化室温离子液体使Au/Pt NPs粒径小、分散均匀,提高有效面积和电子传递;Nafion层选择性透过小分子并阻挡AA、DA等干扰。微透析系统连续采集纹状体透析液,使电流实时反映细胞外谷氨酸水平。

检测灵敏度

LOD: 0.17 μM (S/N = 3);线性范围: 0.5 μM–20.0 μM;I (nA) = 0.96C (μM) + 1.60, r = 0.9924;sensitivity: 1.60 ± 0.56 nA μM−1

效应效果

该传感器对0.1 mM抗坏血酸(AA)和10 μM多巴胺(DA)无可测响应,选择性良好。10 μM谷氨酸连续5次测定RSD为3.4%;连续使用至少6天(每天5–6 h)后,对50 μM谷氨酸的电流响应RSD约降低4.5%,4 ℃保存两周保留86%初始活性。微透析相对回收率为24%。纹状体基础谷氨酸为3.01±0.67 μM,与文献1–4 μM相当;KCl刺激增加2.04±0.40 μM,STN电刺激增加4.68±0.30 μM。其LOD低于氧化还原水凝胶平面金电极和聚吡咯膜传感器,与PAMAM树状大分子Pt NPs/MWCNTs传感器相当,适用于神经生理与病理研究。

传感器的构成

  • 基底电极:玻璃碳电极(GC,3 mm)用于在线实验;丝网印刷碳电极(SPCE,3 mm)用于离线实验,作为换能器。
  • 离子液体/壳聚糖膜:[C3(OH)2mim][BF4]与0.5%壳聚糖(chitosan)混合后滴涂,形成羟基官能化室温离子液体膜,稳定并分散纳米粒子。
  • Au/Pt纳米粒子层:在0.5 mol/L H2SO4含HAuCl4和H2PtCl6中于-1.0 V电沉积Au/Pt NPs(2.5±0.2 nm),提供H2O2电催化活性。
  • 识别元件:谷氨酸氧化酶(GlutaOx,8 mg/mL)与0.4%聚乙烯亚胺(PEI)混合滴涂,经25%戊二醛水蒸气交联,特异性催化谷氨酸氧化。
  • Nafion抗干扰层:2.5% Nafion滴涂覆盖,阻挡抗坏血酸(AA)、多巴胺(DA)、尿酸(UA)等电活性干扰物。

中文摘要

本文合成了一种新型羟基官能化室温离子液体[C3(OH)2mim][BF4],并以该离子液体膜为基底,在其表面电沉积双金属Au/Pt纳米粒子,构建了新型H2O2生物传感器。羟基功能化提供了适宜微环境,使Au/Pt纳米粒子更均匀、更小,平均直径为2.5±0.2 nm。将谷氨酸氧化酶(GlutaOx)固定后,得到GlutaOx-[C3(OH)2mim][BF4]-Au/Pt-Nafion生物传感器,在-200 mV下对谷氨酸表现出优异的电催化响应。作者建立了由微透析泵驱动的在线微透析系统,用于大鼠纹状体谷氨酸的连续检测。该传感器在线微透析系统中对谷氨酸的线性范围为0.5–20.0 μM,检出限为0.17 μM(S/N=3),麻醉大鼠纹状体谷氨酸基础水平为3.01±0.67 μM(n=3)。进一步用于体内监测腹腔注射100 mM KCl和丘脑底核区电刺激时纹状体谷氨酸变化,两种刺激均使细胞外谷氨酸浓度升高。该方法灵敏、可重复,有望应用于生理与病理研究。

英文摘要

A new type of hydroxyl functionalized room temperature ionic liquid (RTIL), [C(3)(OH)(2)mim][BF(4)], was synthesized herein and a novel H(2)O(2) biosensor is fabricated with [C(3)(OH)(2)mim][BF(4)] as the substrate and electrodepositing bimetallic Au/Pt nanoparticles (NPs) onto the [C(3)(OH)(2)mim][BF(4)] film. The functionalization of RTIL with hydroxyl groups provided an appropriate environment for the preparation of more uniform and smaller Au/Pt NPs with the diameter of 2.5 nm±0.2 nm. Immobilized with glutamate oxidase (GlutaOx), the resulting GlutaOx-[C(3)(OH)(2)mim][BF(4)]-Au/Pt-Nafion biosensor displayed excellent electrocatalytic response to glutamate at a potential of -200 mV. An effective on-line microdialysis system, which was powered by a microdialysis pump, was set up and used for the detection of glutamate successively in the striatum of rats. The glutamate biosensor in on-line microdialysis system showed good linear range from 0.5 μM to 20.0 μM with the detection limit of 0.17 μM (S/N=3). The basal level of glutamate in the striatum of anaesthetic rats was calculated to be 3.01±0.67 μM (n=3). The application of the GlutaOx-[C(3)(OH)(2)mim][BF(4)]-Au/Pt-Nafion electrode is further demonstrated for in vivo sensing of the variation of glutamate level in the striatum when rats received intraperitoneal (i.p.) injection of 100 mM KCl and brain electrical stimulation of the subthalamic nucleus area (STN). Both of the two kinds of stimulation resulted in an increase in the extracellular concentration of glutamate. This method has proved to be sensitive and reproducible, which enables its promising application in physiology and pathology.