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基于表面活性剂介导的比色分析联合磁珠上原位滚环扩增检测。

Surfactant-mediated colorimetric assay assisted with in-situ rolling circle amplification on magnetic beads.

机构信息

Qilu University of Technology (Shandong Academy of Sciences), Shandong Analysis and Test Center, Jinan, 250014, China; School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China.

Qilu University of Technology (Shandong Academy of Sciences), Shandong Analysis and Test Center, Jinan, 250014, China; School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China.

出版信息

Anal Chim Acta. 2023 Oct 16;1278:341709. doi: 10.1016/j.aca.2023.341709. Epub 2023 Aug 12.

Abstract

Gold nanoparticles (AuNPs) with localized surface plasmon resonance effect have been widely used for colorimetric detection based on the interparticle plasmon coupling during AuNPs aggregation. However, it is still challenging to develop portable and quantitative methods with good sensitivity and excellent selectivity. In this study, a smartphone-based colorimetric assay is developed on the principle of surfactant-mediated AuNPs aggregation assisted with rolling circle amplification (RCA) on magnetic beads (MBs). The detection of adenosine is demonstrated as an example. The cetyl trimethyl ammonium bromide (CTAB) causes the negatively charged AuNPs to aggregate, which results in the color change from red to blue. When adenosine is in solution, the RCA process is triggered on the MBs because of specific adenosine-aptamer recognition, resulting in prolongation of single-stranded nucleic acid (ssDNA). The solution color remains red due to the electrostatic interaction between CTAB and ssDNA. Using this method, the limit of detection (LOD) for adenosine can be as low as 16 pM. Besides, it also works well in human serum. In addition, a portable device integrated with in-situ RGB analysis software is developed for the detection with a smartphone. This study offers a new strategy to improve the sensitivity and selectivity for the AuNPs-based colorimetric assay, taking advantages of specific aptamer recognition, in-situ RCA on MBs, magnetic separation, and smartphone-based portable device.

摘要

金纳米粒子(AuNPs)具有局域表面等离激元共振效应,已广泛应用于基于 AuNPs 聚集过程中颗粒间等离子体耦合的比色检测。然而,开发具有良好灵敏度和优异选择性的便携式定量方法仍然具有挑战性。在这项研究中,基于胶束介导的 AuNPs 聚集原理,结合磁珠(MBs)上的滚环扩增(RCA),开发了一种基于智能手机的比色分析方法。以腺苷检测为例。十六烷基三甲基溴化铵(CTAB)导致带负电荷的 AuNPs 聚集,导致颜色从红色变为蓝色。当腺苷存在于溶液中时,由于特定的腺苷适体识别,RCA 过程在 MBs 上触发,导致单链核酸(ssDNA)延长。由于 CTAB 和 ssDNA 之间的静电相互作用,溶液颜色保持红色。使用这种方法,腺苷的检测限(LOD)可低至 16 pM。此外,它在人血清中也能很好地工作。此外,还开发了一种集成原位 RGB 分析软件的便携式设备,用于智能手机检测。本研究为基于 AuNPs 的比色分析提供了一种新策略,利用特异性适体识别、MBs 上的原位 RCA、磁分离和基于智能手机的便携式设备,提高了比色分析的灵敏度和选择性。

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