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Self-powered competitive immunosensor driven by biofuel cell based on hollow-channel paper analytical devices

机译:基于空心通道纸质分析装置的生物燃料电池驱动的自供电竞争性免疫传感器

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摘要

A mediator-less and compartment-less glucose/O-2 enzymatic biofuel cell (BFC) was introduced into microfluidic paper-based analytical devices (mu-PADs) that relies on flow in hollow channels with silver nanoparticles/graphene modified paper electrode as the anodic and cathodic substrate, to implement self-powered sensitive carcinoembryonic antigen (CEA) detection. Glucose dehydrogenase (GDH)-gold nanoparticles bioconjugate modified with CEA acted as a biocatalyst for enhancing glucose oxidation in the bioanode, as well as the transducing enzyme for signaling magnification. Similarly, nanoporous PtNi/bilirubin oxidase (BUD) acted as a biocatalyst for enhancing O-2 reduction in the biocathode. With an increase in the concentration of CEA, the amount of CEA-Au-GDH bioconjugate on bioanode decreases, thus leading to the lower output of the as-prepared SEC. This proposed BFC-based self-powered immunosensor for CEA possessed largely increased linear detection range from 1 pg mL(-1) to 0.5 mu g with a detection limit of 0.7 pg mL(-1). The proposed BFC-based self-powered immunosensor shows high sensitivity, stability, and reproducibility and can become a promising platform for other protein detection. (C) 2015 Elsevier B.V. All rights reserved.
机译:无介体和无隔室的葡萄糖/ O-2酶促生物燃料电池(BFC)被引入基于微流体纸的分析装置(mu-PADs)中,该装置依赖于中空通道中的流动,银纳米颗粒/石墨烯修饰的纸电极阳极和阴极底物,以实现自供电的敏感癌胚抗原(CEA)检测。用CEA修饰的葡萄糖脱氢酶(GDH)-金纳米颗粒生物共轭物可作为增强生物阳极中葡萄糖氧化的生物催化剂,以及信号转导放大酶。类似地,纳米多孔PtNi /胆红素氧化酶(BUD)用作增强生物阴极中O-2还原的生物催化剂。随着CEA浓度的增加,生物阳极上的CEA-Au-GDH生物缀合物的量减少,从而导致所制备的SEC的较低输出。提出的基于BFC的CEA自供电免疫传感器具有从1 pg mL(-1)到0.5μg的线性检测范围,并且检测极限为0.7 pg mL(-1)。提出的基于BFC的自供电免疫传感器显示出高灵敏度,稳定性和可重复性,并且可以成为其他蛋白质检测的有前途的平台。 (C)2015 Elsevier B.V.保留所有权利。

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