Department of Biomedical Engineering and Macromolecular Science & Engineering Center, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, Michigan 48109-2099, USA.
Anal Chem. 2010 Apr 15;82(8):3300-5. doi: 10.1021/ac100085w.
This article describes a thin amperometric nitric oxide (NO) sensor that can be microchannel embedded to enable direct real-time detection of NO produced by cells cultured within the microdevice. A key for achieving the thin ( approximately 1 mm) planar sensor configuration required for sensor-channel integration is the use of gold/indium-tin oxide patterned electrode directly on a porous polymer membrane (pAu/ITO) as the base working electrode. The electrochemically deposited Au-hexacyanoferrate layer on pAu/ITO is used to catalyze NO oxidation to nitrite at lower applied potentials (0.65-0.75 V vs Ag/AgCl) and stabilize current output. Furthermore, use of a gas-permeable membrane to separate internal sensor compartments from the sample phase imparts excellent NO selectivity over common interfering agents (e.g., nitrite, ascorbate, ammonia, etc.) present in culture media and biological fluids. The optimized sensor design reversibly detects NO down to the approximately 1 nM level in stirred buffer and <10 nM in flowing buffer when integrated within a polymeric microfluidic device. We demonstrate utility of the channel-embedded sensor by monitoring NO generation from macrophages cultured within non-gas-permeable microchannels, as they are stimulated with endotoxin.
本文描述了一种薄型电流型一氧化氮(NO)传感器,可嵌入微通道中,从而能够直接实时检测微器件内培养的细胞产生的 NO。实现用于传感器-通道集成的薄型(约 1mm)平面传感器结构的关键是使用金/铟锡氧化物图案化电极直接作为基本工作电极在多孔聚合物膜(pAu/ITO)上。在 pAu/ITO 上电沉积的 Au-亚铁氰化钾层用于在较低的施加电位(0.65-0.75V 对 Ag/AgCl)下催化 NO 氧化为亚硝酸盐,并稳定电流输出。此外,使用透气膜将内部传感器隔室与样品相分离,赋予传感器对培养介质和生物流体中存在的常见干扰物(例如亚硝酸盐、抗坏血酸、氨等)的优异 NO 选择性。当集成在聚合物微流控装置内时,优化后的传感器设计可在搅拌缓冲液中以约 1nM 的下限可逆检测到 NO,在流动缓冲液中以<10nM 的下限检测到 NO。我们通过监测在非透气微通道内培养的巨噬细胞在受到内毒素刺激时产生的 NO,证明了通道嵌入式传感器的实用性。