电化学生物传感器 2011

Biosensor microprobes with integrated microfluidic channels for bi-directional neurochemical interaction.

Journal of neural engineering Frey O, van der Wal PD, Spieth S, Brett O, Seidl K, Paul O, Ruther P, Zengerle R, de Rooij NF
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组成图示

Biosensor microprobes with integrated... 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

胆碱(choline, Cho;乙酰胆碱释放替代标志物);样品基质:脑组织细胞外液/脑内微环境,体外PBS及琼脂糖凝胶脑幻影

检测原理

胆碱从脑组织或微流控通道扩散至电极表面,先穿过m-PPD半透膜,再进入ChoOx/BSA/GA酶膜。ChoOx催化胆碱氧化并生成H2O2;H2O2在Pt微电极表面于0.7 V(vs Ag/AgCl)发生电化学氧化,产生与胆碱浓度成正比的安培电流。m-PPD膜可排斥多巴胺、抗坏血酸等电活性干扰物,提高选择性;相邻仅含BSA/GA的负控电极用于差分扣除背景。微流控通道可在电极附近局部输送胆碱或刺激物,实现同一探针杆上的同时化学刺激与记录。该体系无HCR/RCA等核酸放大,主要依靠酶催化生成H2O2实现化学放大。

检测灵敏度

LOD: 低于1 μM;灵敏度: 优于10 pA/μM;一个月后灵敏度: 3 pA/μM

效应效果

在PBS 37 °C中,对10 μM胆碱快速响应,t90%=2 s;对2 μM多巴胺和200 μM抗坏血酸无明显电流响应,说明m-PPD抗干扰有效。所有活性电极灵敏度与选择性一致,非活性电极无响应,表明平行膜沉积重现性好且无串扰,可作差分负控。功能化后第一个月灵敏度下降,m-PPD对DA/AA略渗透,但3 pA/μM仍满足体内测量,LOD<1 μM,货架寿命至少一个月。微流控通道流速至5 μl/min无泄漏,死体积<700 nl。琼脂糖凝胶脑幻影中同时注射1 mM胆碱200 nl并记录,活性电极出现立即电流峰,非活性无响应,证明同一探针杆可同时化学刺激与记录。作者认为其适用于脑内胆碱/乙酰胆碱释放的时空分辨监测。

传感器的构成

  • 基底/换能器:硅微探针(silicon microprobe),双探针杆与微流控通道,提供机械支撑和局部液体输送
  • 绝缘/钝化层:热氧化SiO2与LPCVD Si3N4(各200 nm)及顶层PECVD SiO2/Si3N4,隔离电极并开孔
  • 微电极:铂(Pt)微电极,50 μm×150 μm凹陷工作电极;80 μm×1200 μm Pt参考/对电极,可沉积Ag/AgCl
  • 识别/催化层:胆碱氧化酶(ChoOx)/牛血清白蛋白(BSA)/戊二醛(GA)酶膜,电化学辅助吸附固定,催化胆碱生成H2O2
  • 抗干扰/半透膜:m-苯二胺(m-PD)电化学聚合膜(m-PPD),排斥多巴胺(DA)和抗坏血酸(AA)等干扰物
  • 负控/差分膜:仅BSA/GA蛋白膜加m-PPD,匹配扩散并作为差分测量负控
  • 封装/互连:聚碳酸酯(PC)支架、O形圈、ZEBRA连接器和PCB,提供可逆流体与电连接

中文摘要

本文报道了一种硅基微探针,长8 mm,截面250 μm×250 μm,每根探针杆集成4个凹陷生物传感器微电极(50 μm×150 μm),电极表面涂覆酶层,用于在脑组织多个部位选择性检测胆碱。同一探针杆内还集成最多两个微流控通道,可在距生物传感器微电极定义距离处进行受控局部液体输送。采用先进硅微加工技术可重复制备这些按实验需求定制的多功能探针阵列。自制支架保证微探针可靠的电连接和流体连接;可逆封装方法显著降低成本和装配时间,并简化连续实验之间生物传感器探针的储存。电极功能化采用电化学辅助吸附,这种空间可控沉积技术可实现膜层平行沉积,尤其适用于微电极阵列。所获生物传感器具有足够性能,可在生理相关浓度下以足够的时间与空间分辨率检测胆碱,用于脑研究。对胆碱的灵敏度优于10 pA/μM,检出限低于1 μM,响应时间为2 s。将生物传感器与微流控注射器集成于同一微探针,可在琼脂糖凝胶脑幻影中实现同时化学刺激与记录。

英文摘要

This paper reports on silicon-based microprobes, 8 mm long and 250 µm × 250 µm cross-section, comprising four recessed biosensor microelectrodes (50 µm × 150 µm) per probe shank coated with an enzymatic layer for the selective detection of choline at multiple sites in brain tissue. Integrated in the same probe shank are up to two microfluidic channels for controlled local liquid delivery at a defined distance from the biosensor microelectrodes. State-of-the-art silicon micromachining processing was applied for reproducible fabrication of these experiment-tailored multi-functional probe arrays. Reliable electric and fluidic interconnections to the microprobes are guaranteed by a custom-made holder. The reversible packaging method implemented in this holder significantly reduces cost and assembly time and simplifies storage of the biosensor probes between consecutive experiments. The functionalization of the electrodes is carried out using electrochemically aided adsorption. This spatially controlled deposition technique enables a parallel deposition of membranes and is especially useful when working with microelectrode arrays. The achieved biosensors show adequate characteristics to detect choline in physiologically relevant concentrations at sufficient temporal and spatial resolution for brain research. Sensitivity to choline better than 10 pA µm(-1), detection limit below 1 µM and response time of 2 s were obtained. The proposed combination of biosensors and microfluidic injectors on the same microprobe allows simultaneous chemical stimulation and recording as demonstrated in an agarose gel-based brain phantom.