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镍/氧化镍纳米颗粒与微流控酶联免疫吸附测定芯片的集成,以生成用于检测的传感平台。

Integration of Ni/NiO nanoparticles and a microfluidic ELISA chip to generate a sensing platform for detection.

作者信息

Weng Chang-Ching, Chao Chien-Yu, Wu She-Ting, Tsou Ping-Hsien, Chen Wei-Tin, Li Bor-Ran, Li Yaw-Kuen

机构信息

Department of Applied Chemistry, College of Science, Yang Ming Chiao Tung University Hsinchu Taiwan.

Institute of Biomedical Engineering, College of Electrical and Computer Engineering, Yang Ming Chiao Tung University Hsinchu Taiwan

出版信息

RSC Adv. 2021 Aug 24;11(46):28551-28556. doi: 10.1039/d1ra04631d. eCollection 2021 Aug 23.

Abstract

Enzyme-linked immunosorbent assays (ELISAs) are tests that uses antibody recognition and enzyme catalytic activity to identify a substance, and they have been widely used as a diagnostic tool in the clinic. However, performing an ELISA requires various liquid handling steps and long binding times. To solve this problem, we developed a magnetic microfluidic ELISA system (MMF-ELISA). Integration with nickel magnetic nanoparticles can streamline the ELISA process in a fully automated manner for detection. First, we synthesized paramagnetic surface-oxidized nickel nanoparticles (Ni/NiO NPs) to carry protein G. Then, we assembled a SUM290 (UlaG)-specific antibody on protein G. Finally, we integrated the NPs on a microfluidics chip for detection. The chip contains three different layers to trap the solutions; the bottom layer SiO is patterned on hydrophobic polymers and integrated with the middle layer PDMS and the top layer PMMA. With Arduino and motor IC, we developed an automated platform for detection. Microfluidic ELISAs can reduce the manual handling and operation time. Furthermore, the developed system can be extended to multiple areas for ELISA-related assays. This economical, rapid and portable system may become a promising platform for sensing in clinical applications.

摘要

酶联免疫吸附测定(ELISA)是利用抗体识别和酶催化活性来鉴定物质的检测方法,已在临床中广泛用作诊断工具。然而,进行ELISA需要各种液体处理步骤和较长的结合时间。为了解决这个问题,我们开发了一种磁性微流控ELISA系统(MMF-ELISA)。与镍磁性纳米颗粒集成可以以全自动方式简化ELISA检测过程。首先,我们合成了携带蛋白G的顺磁性表面氧化镍纳米颗粒(Ni/NiO NPs)。然后,我们在蛋白G上组装了SUM290(UlaG)特异性抗体。最后,我们将纳米颗粒集成到微流控芯片上进行检测。该芯片包含三层以捕获溶液;底层SiO图案化在疏水聚合物上,并与中间层PDMS和顶层PMMA集成。借助Arduino和电机集成电路,我们开发了一个自动化检测平台。微流控ELISA可以减少人工操作和运行时间。此外,所开发的系统可以扩展到多个领域用于ELISA相关检测。这种经济、快速且便携的系统可能成为临床应用中传感的一个有前景的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582d/9038132/0e04957918be/d1ra04631d-f1.jpg

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