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Sensitive glucometer-based microfluidic immune-sensing platform via DNA signal amplification coupled with enzymatic reaction
Sensors and Actuators B: Chemical ( IF 8.4 ) Pub Date : 2020-11-25 , DOI: 10.1016/j.snb.2020.129055
Yu Gu , Xuejiao Yang , Shanwen Hu , Chunxian Guo , Bo Chen , Cunxia Fan , Chang Ming Li

Here we present a novel glucometer-based microfluidic platform using miniaturized personal glucose meter (PGM) with portability and simple operation to sensitively detect cancer biomarker via amplification of rolling cycle amplification (RCA) associated with DNA-invertase catalysis. This design utilizes gold nanoparticles (Au NPs) as a supporting matrix to anchor Human Epidermal Growth Factor Receptor 2 antibody (anti-HER2) and DNA sequence that is able to induce RCA. After adding HER2, a sandwiches immunocomplex forms between a peptide and the asymmetric DNA-anti-HER2-modified Au NPs in the detection area of a glass slide, followed by RCA process and hybridization of the RCA products with DNA-invertase for enzymatic generation of glucose. In such a way, RCA-amplified DNA converted glucose can be detected by PGM for sensitively diagnosis of HER2 biomarker. This assay is performed on a 43 × 43 mm microfluidic chip with small reagent volume, large dynamic range and high sensitivity, holding great promise in the clinical diagnosis at home or in urban area.



中文翻译:

通过基于DNA信号放大和酶促反应的基于血糖仪的微流控免疫敏感平台

在这里,我们介绍了一种新型的基于葡萄糖计的微流控平台,该平台使用便携式个人血糖仪(PGM)具有便携性和简单的操作,可以通过与DNA转化酶催化相关的滚动循环扩增(RCA)的扩增来灵敏地检测癌症生物标志物。该设计利用金纳米颗粒(Au NPs)作为支持基质,锚定人类表皮生长因子受体2抗体(anti-HER2)和能够诱导RCA的DNA序列。加入HER2后,在载玻片的检测区域中,在肽和不对称的DNA-抗-HER2修饰的Au NP之间形成夹心免疫复合物,然后进行RCA处理,并将RCA产物与DNA转化酶杂交以酶促生成葡萄糖。以这样的方式,可以通过PGM检测RCA扩增的DNA转化的葡萄糖,以灵敏地诊断HER2生物标志物。该测定法在试剂体积小,动态范围大,灵敏度高的43×43 mm微流控芯片上进行,在家庭或城市地区的临床诊断中具有广阔的前景。

更新日期:2020-12-11
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