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基于金纳米双子星@MnO 纳米片纳米结构的酶诱导刻蚀的等离子体比色生物传感器用于灵敏的外泌体检测

Plasmonic Colorimetric Biosensor for Sensitive Exosome Detection via Enzyme-Induced Etching of Gold Nanobipyramid@MnO Nanosheet Nanostructures.

机构信息

Research Center for Analytical Sciences, Northeastern University, Shenyang 110819, P. R. China.

出版信息

Anal Chem. 2020 Nov 17;92(22):15244-15252. doi: 10.1021/acs.analchem.0c04136. Epub 2020 Oct 27.

DOI:10.1021/acs.analchem.0c04136
PMID:33108733
Abstract

Exosomes involved in tumor-specific processes display excellent potential in the early diagnosis of cancer. Herein, a highly sensitive plasmonic colorimetric biosensor was proposed for exosome quantification. The sensing strategy mainly includes two steps: exosome-triggered competitive reaction and etching of gold nanobipyramid@MnO nanosheet nanostructures (Au NBP@MnO NSs). A competitive reaction between exosomes and placeholder chains induced by exosomes can translate the signal of exosomes into the amount of alkaline phosphatase, which simplifies the experimental process and amplifies the signal. The etching of Au NBP@MnO NSs by ascorbic acid generated from the hydrolysis of l-ascorbic acid 2-phosphate by alkaline phosphatase changes the refractive index of Au NBPs, accompanied by the blue shift of the longitudinal localized surface plasmon resonance peak. Profiting from the signal amplification of the competitive reaction and superior refractive index sensitivity of colorimetric substrates, this protocol exhibits high sensitivity toward exosomes within 8.5 × 10 to 8.5 × 10 particles μL, along with a detection limit of 1.35 × 10 particles μL, which is more sensitive than previously reported colorimetric methods. In addition, a sensitive multicolor visual detection of exosomes was realized by adjusting the aspect ratio of Au NBPs. It is worth mentioning that the Au NBP@MnO NSs was synthesized through in situ growth of MnO nanosheets on Au NBPs, and the attractive optical properties and ease of etching make Au NBP@MnO NSs promising candidates for plasmonic detection.

摘要

外泌体参与肿瘤特异性过程,在癌症的早期诊断中显示出巨大的潜力。在此,提出了一种用于外泌体定量的高灵敏等离子体比色生物传感器。该传感策略主要包括两个步骤:外泌体触发的竞争反应和金纳米双锥@MnO 纳米片纳米结构(Au NBP@MnO NSs)的蚀刻。外泌体引发的外泌体和占位链之间的竞争反应可以将外泌体的信号转化为碱性磷酸酶的量,从而简化了实验过程并放大了信号。碱性磷酸酶水解 l-抗坏血酸 2-磷酸产生的抗坏血酸使 Au NBP@MnO NSs 发生蚀刻,从而改变 Au NBPs 的折射率,同时伴随着纵向局域表面等离子体共振峰的蓝移。得益于竞争反应的信号放大和比色基底的卓越折射率灵敏度,该方案在 8.5×10 至 8.5×10 个颗粒 μL 的范围内对外泌体表现出高灵敏度,检测限低至 1.35×10 个颗粒 μL,比以前报道的比色方法更灵敏。此外,通过调整 Au NBPs 的纵横比,可以实现对外泌体的灵敏多色可视化检测。值得一提的是,Au NBP@MnO NSs 通过 MnO 纳米片在 Au NBPs 上的原位生长合成,其吸引人的光学性质和易于蚀刻性使 Au NBP@MnO NSs 成为等离子体检测的有前途的候选材料。

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