Hulvey Matthew K, Martin R Scott
Department of Chemistry, Saint Louis University, 3501 Laclede Avenue, St. Louis, MO 63103, USA.
Anal Bioanal Chem. 2009 Jan;393(2):599-605. doi: 10.1007/s00216-008-2468-z. Epub 2008 Nov 7.
This paper describes the fabrication and characterization of a microfluidic device that utilizes a reservoir-based approach for endothelial cell immobilization and integrated embedded carbon ink microelectrodes for the amperometric detection of extracellular nitric oxide (NO) release. The design utilizes a buffer channel to continuously introduce buffer or a plug of stimulant to the reservoir as well as a separate sampling channel that constantly withdraws buffer from the reservoir and over the microelectrode. A steel pin is used for both the fluidic connection to the sampling channel and to provide a quasi-reference electrode for the carbon ink microelectrode. Characterization of the device was performed using NO standards produced from a NONOate salt. Finally, NO release from a layer of immobilized endothelial cells was monitored and quantified using the system. This system holds promise as a means to electrochemically detect extracellular NO release from endothelial cells in either an array of reservoirs or concurrently with fluorescence-based intracellular NO measurements.
本文描述了一种微流控装置的制造与表征,该装置采用基于储液器的方法固定内皮细胞,并集成嵌入式碳墨微电极用于安培检测细胞外一氧化氮(NO)释放。该设计利用一个缓冲通道将缓冲液或刺激剂塞持续引入储液器,以及一个单独的采样通道,该通道不断从储液器中抽取缓冲液并流经微电极。一根钢针用于与采样通道进行流体连接,并为碳墨微电极提供准参比电极。使用由NONOate盐产生的NO标准品对该装置进行表征。最后,使用该系统监测并定量了固定化内皮细胞层释放的NO。该系统有望成为一种手段,用于电化学检测储液器阵列中内皮细胞释放的细胞外NO,或与基于荧光的细胞内NO测量同时进行检测。