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使用透明氧化铟锡电极对量子化儿茶酚胺释放进行片上安培测量。

On-chip amperometric measurement of quantal catecholamine release using transparent indium tin oxide electrodes.

作者信息

Sun Xiuhua, Gillis Kevin D

机构信息

Dalton Cardiovascular Research Center, Department of Biological Engineering, University of Missouri-Columbia, Columbia, Missouri 65211, USA.

出版信息

Anal Chem. 2006 Apr 15;78(8):2521-5. doi: 10.1021/ac052037d.

DOI:10.1021/ac052037d
PMID:16615759
Abstract

Carbon-fiber amperometry has been extensively used to monitor the time course of catecholamine release from cells as individual secretory granules discharge their contents during the process of quantal exocytosis, but microfabricated devices offer the promise of higher throughput. Here we report development of a microchip device that uses transparent indium tin oxide (ITO) electrodes to measure quantal exocytosis from cells in microfluidic channels. ITO films on a glass substrate were patterned as 20-mum-wide stripes using photolithography and wet etching and then coated with polylysine to facilitate cell adherence. Microfluidic channels (100 mum wide by 100 mum deep) were formed by molding poly(dimethylsiloxane) (PDMS) on photoresist and then reversibly sealing the PDMS slab to the ITO-glass substrate. Bovine adrenal chromaffin cells were loaded into the microfluidic channel and adhered to the ITO electrodes. Cells were stimulated to secrete by perfusing a depolarizing "high-K" solution while monitoring oxidation of catecholamines on the ITO electrode beneath the cell using amperometry. Amperometric spikes with charges ranging from 0.1 to 1.5 pC were recorded with a signal-to-noise ratio comparable to that of carbon-fiber electrodes. Further development of this approach will enable high-throughput measurement of quantal catecholamine release simultaneously with optical cell measurements such as fluorescence.

摘要

碳纤维安培法已被广泛用于监测细胞中儿茶酚胺释放的时间进程,因为在量子胞吐过程中单个分泌颗粒会释放其内容物,但微加工设备有望实现更高的通量。在此,我们报告了一种微芯片设备的开发,该设备使用透明氧化铟锡(ITO)电极来测量微流体通道中细胞的量子胞吐。使用光刻和湿蚀刻将玻璃基板上的ITO薄膜图案化为20微米宽的条纹,然后涂覆聚赖氨酸以促进细胞粘附。通过在光刻胶上模制聚二甲基硅氧烷(PDMS),然后将PDMS平板可逆地密封到ITO玻璃基板上,形成微流体通道(宽100微米,深100微米)。将牛肾上腺嗜铬细胞加载到微流体通道中并粘附到ITO电极上。在使用安培法监测细胞下方ITO电极上儿茶酚胺氧化的同时,通过灌注去极化的“高钾”溶液刺激细胞分泌。记录到电荷范围为0.1至1.5 pC的安培尖峰,其信噪比与碳纤维电极相当。这种方法的进一步发展将能够在进行诸如荧光等光学细胞测量的同时,对儿茶酚胺的量子释放进行高通量测量。

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