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首页> 外文期刊>Bulletin of the Korean Chemical Society >An Electrochemical Enzyme Immunochip Based on Capacitance Measurement for the Detection of IgG
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An Electrochemical Enzyme Immunochip Based on Capacitance Measurement for the Detection of IgG

机译:基于电容测量的电化学酶免疫芯片检测IgG

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This study describes the development of an electrochemical array immunochip for the detection of IgG. Interdigitated immunochip platforms were fabricated by sputtering gold on a glass wafer by using MEMS process and then were coated with Eudragit S100, an enteric polymer, forming an insulating layer over the working area of immunochips. The breakdown of the polymer layer was exemplified by the catalytic action of urease which, in the presence of urea, caused an alkaline pH change. This subsequently caused an increase of the double layer capacitance of the underlying electrode. Used in conjunction with a competitive immunoassay format, this allowed the ratio of initial to final electrode capacitance to be directly linked with the concentration of analyte, i.e. IgG. Responses to IgG could be detected at IgG concentration as low as 250 ngmL−1 and showed good linearity up to IgG concentration as high as 20 μgmL−1.
机译:这项研究描述了用于检测IgG的电化学阵列免疫芯片的开发。通过使用MEMS工艺在玻璃晶片上溅射金来制造相互交叉的免疫芯片平台,然后用肠溶聚合物Eudragit S100涂覆,在免疫芯片的工作区域上形成绝缘层。聚合物层的分解以脲酶的催化作用为例,脲酶在脲存在下引起碱性pH值变化。随后,这导致下面的电极的双层电容增加。与竞争性免疫测定法结合使用,可以使初始电极电容与最终电极电容的比率与分析物(即IgG)的浓度直接相关。在低至250 ngmL-1的IgG浓度下就可以检测到对IgG的响应,并且在高至20μgmL-1的IgG浓度下表现出良好的线性。

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