Biomicrofluidics. 2011 Sep;5(3):32008-3200811. doi: 10.1063/1.3624739. Epub 2011 Sep 20.
Seamless integration of biological components with electrochemical sensors is critical in the development of microdevices for cell analysis. The present paper describes the integration miniature Au electrodes next to immune cells (macrophages) in order to detect cell-secreted hydrogen peroxide (H(2)O(2)). Photopatterning of poly(ethylene glycol) (PEG) hydrogels was used to both immobilize horseradish peroxidase molecules onto electrodes and to define regions for cell attachment in the vicinity of sensing electrodes. Electrodes micropatterned in such a manner were enclosed inside poly(dimethylsiloxane) fluid conduits and incubated with macrophages. The cells attached onto the exposed glass regions in the vicinity of the electrodes and nowhere else on the non-fouling PEG hydrogel surface. A microfluidic device was converted into an electrochemical cell by placing flow-through Ag∕AgCl reference and Pt wire counter electrodes at the outlet and inlet, respectively. This microdevice with integrated H(2)O(2)-sensing electrodes had sensitivity of 27 μA∕cm(2) mM with a limit of detection of 2 μM. Importantly, this microdevice allowed controllable seeding of macrophages next to electrodes, activation of these cells and on-chip monitoring of H(2)O(2) release in real time. In the future, this biosensor platform may be utilized for monitoring of macrophage responses to pathogens or for the study of inflammatory signaling in micropatterned cell cultures.
将生物元件与电化学传感器无缝集成是开发用于细胞分析的微器件的关键。本文描述了将微型 Au 电极集成到免疫细胞(巨噬细胞)旁边,以便检测细胞分泌的过氧化氢(H2O2)。聚乙二醇(PEG)水凝胶的光图案化用于将辣根过氧化物酶分子固定在电极上,并在靠近传感电极的区域定义细胞附着的区域。以这种方式微图案化的电极被封闭在聚二甲基硅氧烷(PDMS)流体管道内,并与巨噬细胞孵育。细胞附着在电极附近暴露的玻璃区域,而不在无缺陷的 PEG 水凝胶表面的其他任何地方。通过将流通式 Ag∕AgCl 参比电极和 Pt 丝对电极分别放置在出口和入口处,将微流体装置转换为电化学池。这种带有集成 H2O2 传感电极的微器件的灵敏度为 27 μA∕cm2mM,检测限为 2 μM。重要的是,这种微器件允许在电极旁边可控地接种巨噬细胞,激活这些细胞,并在芯片上实时监测 H2O2 的释放。在未来,这种生物传感器平台可用于监测巨噬细胞对病原体的反应,或用于研究微图案化细胞培养物中的炎症信号传导。