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

机译:使用透明铟锡氧化物电极的片上安培法测量儿茶酚胺的定量释放

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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-mu m-wide stripes using photolithography and wet etching and then coated with polylysine to facilitate cell adherence. Microfluidic channels (100 mu m wide by 100 pm 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.
机译:碳纤维安培法已被广泛用于监测儿茶酚胺从细胞中释放出来的时间过程,因为各个分泌颗粒在定量胞吐过程中会释放其含量,但微制造设备有望提供更高的通量。在这里,我们报告使用透明的铟锡氧化物(ITO)电极来测量微流控通道中的细胞的定量胞吐作用的微芯片设备的开发。使用光刻和湿蚀刻将玻璃基板上的ITO膜图案化为20微米宽的条纹,然后涂上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)形成微流体通道(宽100微米,深100微米),然后将PDMS平板可逆地密封到ITO玻璃基板上。牛肾上腺嗜铬细胞被加载到微流控通道并粘附到ITO电极上。通过使用去极化的“高K”溶液刺激细胞分泌,同时使用安培法监测细胞下方ITO电极上儿茶酚胺的氧化。记录的电荷在0.1到1.5 pC范围内的安培峰,其信噪比与碳纤维电极相当。这种方法的进一步发展将使定量儿茶酚胺释放的高通量测量与光学细胞测量(例如荧光)同时进行。

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