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通过具有可控流体分离器的氧化铜纳米花功能化纸基芯片实现过氧化物酶转移增强光电化学适体传感。

Mimic peroxidase-transfer enhancement of photoelectrochemical aptasensing via CuO nanoflowers functionalized lab-on-paper device with a controllable fluid separator.

机构信息

School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China.

School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China; School of Materials Science and Engineering, University of Jinan, Jinan 250022, PR China.

出版信息

Biosens Bioelectron. 2019 May 15;133:32-38. doi: 10.1016/j.bios.2019.02.027. Epub 2019 Feb 19.

Abstract

Inspired by the design of folding greeting cards and tissue drawing covers, a photoelectrochemical (PEC) lab-on-paper device with a controllable fluid separator, producing both reaction zone and detection zone, was explored for ultrasensitive detection of adenosine 5'-triphosphate (ATP) via mimic peroxidase-transfer enhancement of photocurrent response. To realize it, the DNA1, aptamer, and DNA2 as well as the mimic peroxidase of G-quadruplex/hemin modified Au nanocubes were linked on the graphene oxide-functionalized reaction zone via the DNA hybridization. Meanwhile, three-dimensional CuO nanoflowers (CuO NFs) as a photoactive material with outstanding electron transfer ability and absorption of light were grown in situ on the detection zone, providing a PEC active interface. Besides, an innovative fluid separator was elaborately designed by assembling a strip of paper with a hydrophilic channel, providing an effective way to bridge the gap between the two zones with a controllable drawing way, which could successfully avoid the signal interference caused by modifying biomolecules layer by layer on photosensitive materials. In the presence of ATP, the G-quadruplex/hemin modified in the reaction zone was dissociated due to the specific recognition of ATP with aptamer and released into the detection zone with the assistance of controllable fluid separator. The free G-quadruplex/hemin could catalyze hydrogen peroxide to generate oxygen for the consumption of photo-induced electrons from CuO NFs, which could further promote the electron-hole carriers separation efficiency, and eventually resulting in the enhancement of PEC signal. The proposed PEC lab-on-paper device could be employed for specific detection of ATP in the range from 5.0 to 3.0 × 10 nM with a detection limit of 2.1 nM.

摘要

受折叠贺卡和纸巾绘图封面设计的启发,设计了一种光电化学(PEC)纸基芯片装置,该装置具有可控的流体分离器,可同时产生反应区和检测区,用于通过模拟过氧化物酶转移增强光电流响应来超灵敏检测 5'-三磷酸腺苷(ATP)。为了实现这一目标,通过 DNA 杂交将 DNA1、适体和 DNA2 以及修饰的金纳米立方体的模拟过氧化物酶 G-四链体/血红素连接到功能化的反应区的石墨烯氧化物上。同时,原位生长三维氧化铜纳米花(CuO NFs)作为一种具有出色电子转移能力和光吸收能力的光活性材料,在检测区上提供了一个 PEC 活性界面。此外,通过组装一条带有亲水通道的纸条,精心设计了一种创新的流体分离器,提供了一种用可控的拉动方式桥接两个区域的有效方法,从而可以成功避免通过在光敏材料上逐层修饰生物分子引起的信号干扰。在存在 ATP 的情况下,由于适体对 ATP 的特异性识别,反应区中修饰的 G-四链体/血红素会解离,并在可控流体分离器的协助下释放到检测区。游离的 G-四链体/血红素可以催化过氧化氢生成氧气,用于消耗 CuO NFs 的光致电子,从而进一步提高电子空穴载流子分离效率,最终增强 PEC 信号。所提出的 PEC 纸基芯片装置可用于在 5.0 至 3.0×10 nM 的范围内对 ATP 进行特异性检测,检测限为 2.1 nM。

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