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三维电影般的纳米酶具有协同放大效应,可用于呼吸道病毒的超灵敏免疫层析检测。

3D Film-Like Nanozyme with a Synergistic Amplification Effect for the Ultrasensitive Immunochromatographic Detection of Respiratory Viruses.

机构信息

Department of Clinical Laboratory Medicine, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong 510000, China.

出版信息

ACS Nano. 2024 Sep 17;18(37):25865-25879. doi: 10.1021/acsnano.4c09513. Epub 2024 Sep 2.

Abstract

Greatly improving the sensitivity and detection range of lateral flow immunoassays (LFAs) by at least 100 times without using additional instruments remains challenging. Herein, we develop a three-dimensional (3D) film-like nanozyme (GO-Pt-AuPt) by ordered assembly of one layer of 30 nm Pt nanoparticles (NPs) and one layer of small Au@Pt satellites (5 nm) onto a two-dimensional (2D) graphene oxide (GO) nanofilm, in which GO greatly increased the interface area and stability of the nanozyme whereas Pt and Au@Pt NPs synergistically enhanced colorimetric/catalytic activities. The grafting of outer Au@Pt satellites converted the 2D nanofilm into a 3D flexible nanozyme with numerous catalytic sites for enzymatic deposition signal amplification and binding sites for target capture. The introduction of GO-Pt-AuPt into multiplex LFA achieved the ultrasensitive and simultaneous detection of two important respiratory viruses with sensitivity of 1 pg/mL level, which was about 100 times higher than that without signal enrichment and at least 20 and 1900 times higher than those of traditional enzyme-linked immunosorbent assay and AuNP-based LFA, respectively. The clinical utility of the proposed assay was validated through the diagnosis of 49 real clinical respiratory tract specimens. Our proposed LFA shows great potential for the ultrasensitive screening of pathogens in the field.

摘要

在不使用额外仪器的情况下,将侧向流动免疫分析(LFA)的灵敏度和检测范围至少提高 100 倍仍然具有挑战性。在此,我们通过将一层 30nm 的 Pt 纳米颗粒(NPs)和一层 5nm 的小 Au@Pt 卫星(satellites)有序组装到二维(2D)氧化石墨烯(GO)纳米薄膜上,开发了一种三维(3D)薄膜状纳米酶(GO-Pt-AuPt),其中 GO 极大地增加了纳米酶的界面面积和稳定性,而 Pt 和 Au@Pt NPs 协同增强了比色/催化活性。外部 Au@Pt 卫星的接枝将二维纳米薄膜转化为具有许多催化位点的 3D 柔性纳米酶,用于酶沉积信号放大和目标捕获的结合位点。将 GO-Pt-AuPt 引入多重 LFA 实现了两种重要呼吸道病毒的超灵敏和同时检测,灵敏度达到 pg/mL 级,比没有信号富集时提高了约 100 倍,比传统酶联免疫吸附测定法和基于 AuNP 的 LFA 分别提高了 20 倍和 1900 倍。通过对 49 份真实临床呼吸道标本的诊断验证了该检测方法的临床实用性。我们提出的 LFA 具有在现场超灵敏筛选病原体的巨大潜力。

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