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基于注射器驱动过滤装置的用于 SARS-CoV-2 检测的简单且超灵敏的纳米酶联免疫吸附测定法。

Simple and Ultrasensitive Nanozyme-Linked Immunosorbent Assay for SARS-CoV-2 Detection on a Syringe-Driven Filtration Device.

机构信息

Bioinformatics Center of AMMS, Beijing 100850, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 28;16(34):44485-44492. doi: 10.1021/acsami.4c08787. Epub 2024 Aug 16.

DOI:10.1021/acsami.4c08787
PMID:39150764
Abstract

This work proposed a simple and ultrasensitive nanozyme-based immunoassay on a filtration device for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid protein (NP). Gold core porous platinum shell nanoparticles (Au@Pt NPs) were synthesized with high catalytic activity to oxidize 3,3',5,5'-tetramethylbenzidine, leading to an oblivious color change. The filtration device was designed based on the size difference of magnetic beads, filter membrane pore, and Au@Pt NPs. A simple, rapid, and consistent washing procedure can be performed with the help of a plastic syringe. This detection method could realize the quantitative detection of SARS-CoV-2 NP within 80 min for point-of-care needs. The limit of detection for the SARS-CoV-2 antigen was 0.01 ng/mL in buffer. The coefficients of variation of the assay were 1.78% for 10 ng/mL SARS-CoV-2 antigen, 2.03% for 1 ng/mL SARS-CoV-2 antigen, and 2.34% for the negative sample, respectively. The specificity of the detection platform was verified by the detection of various respiratory viruses. This simple and effective detection system was expected to promote substantial progress in the development and application of virus immunodetection technology.

摘要

这项工作提出了一种基于纳米酶的简单且超灵敏免疫分析方法,用于在过滤装置上检测严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)核衣壳蛋白(NP)。金核多孔铂壳纳米粒子(Au@Pt NPs)具有高催化活性,可氧化 3,3',5,5'-四甲基联苯胺,导致颜色不可见的变化。该过滤装置是基于磁珠、滤膜孔和 Au@Pt NPs 的大小差异设计的。在塑料注射器的帮助下,可以进行简单、快速且一致的洗涤程序。这种检测方法可以满足即时检测的需求,在 80 分钟内实现 SARS-CoV-2 NP 的定量检测。在缓冲液中,SARS-CoV-2 抗原的检测限为 0.01 ng/mL。对于 10 ng/mL SARS-CoV-2 抗原、1 ng/mL SARS-CoV-2 抗原和阴性样本,该测定的变异系数分别为 1.78%、2.03%和 2.34%。通过检测各种呼吸道病毒验证了检测平台的特异性。这种简单有效的检测系统有望推动病毒免疫检测技术的发展和应用取得重大进展。

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