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电泳辅助的纳米粒子多层组装用于灵敏的侧向流动免疫分析。

Electrophoresis-Assisted Multilayer Assembly of Nanoparticles for Sensitive Lateral Flow Immunoassay.

机构信息

Department of Chemistry, York University, 4700 Keele Street, Toronto, Ontario M3J 1P3, Canada.

Centre for Research on Biomolecular Interactions, York University, 4700 Keele Street, Toronto, Ontario M3J 1P3, Canada.

出版信息

Angew Chem Int Ed Engl. 2023 Jan 9;62(2):e202215548. doi: 10.1002/anie.202215548. Epub 2022 Dec 7.

Abstract

Lateral flow immunoassay (LFIA) is a rapid, simple, and inexpensive point-of-need method. A major limitation of LFIA is a high limit of detection (LOD), which impacts its diagnostic sensitivity. To overcome this limitation, we introduce a signal-enhancement procedure that is performed after completing LFIA and involves controllably moving biotin- and streptavidin-functionalized gold nanoparticles by electrophoresis. The nanoparticles link to immunocomplexes forming multilayer aggregates on the test strip, thus, enhancing the signal. Here, we demonstrate lowering the LOD of hepatitis B surface antigen from approximately 8 to 0.12 ng mL , making it clinically acceptable. Testing 118 clinical samples for hepatitis B showed that signal enhancement increased the diagnostic sensitivity of LFIA from 73 % to 98 % while not affecting its 95 % specificity. Electrophoresis-driven enhancement of LFIA is universal (antigen-independent), takes two minutes, and can be performed by an untrained person.

摘要

侧向流动免疫分析(LFIA)是一种快速、简单且经济实惠的即时检测方法。LFIA 的主要限制是检测限(LOD)较高,这会影响其诊断灵敏度。为了克服这一限制,我们引入了一种信号增强程序,该程序在完成 LFIA 后进行,涉及通过电泳可控地移动生物素和链霉亲和素功能化的金纳米粒子。纳米粒子与免疫复合物结合,在测试条上形成多层聚集体,从而增强信号。在这里,我们证明可以将乙型肝炎表面抗原的 LOD 从约 8ng/mL 降低到 0.12ng/mL,使其达到临床可接受的水平。对 118 份乙型肝炎临床样本的检测表明,信号增强将 LFIA 的诊断灵敏度从 73%提高到 98%,而不会影响其 95%的特异性。电泳驱动的 LFIA 增强是通用的(与抗原无关),耗时两分钟,并且可以由未经训练的人员进行。

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