基于双金纳米粒子缀合物的心肌肌钙蛋白 I 侧向流动分析检测方法。

A dual gold nanoparticle conjugate-based lateral flow assay (LFA) method for the analysis of troponin I.

机构信息

Biomonitoring Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 111 Gwahangno, Yuseong-gu, Daejeon 305-806, Republic of Korea.

出版信息

Biosens Bioelectron. 2010 Apr 15;25(8):1999-2002. doi: 10.1016/j.bios.2010.01.019. Epub 2010 Jan 25.

Abstract

For signal amplification without an additional operation step in a gold nanoparticle (AuNP)-based lateral flow assay (LFA), a new and simple method utilizing two AuNP-antibody conjugates was developed. The 1st conjugate was the AuNP immobilized with an anti-troponin I antibody and blocked with bovine serum albumin (BSA), and the 2nd conjugate was the AuNP immobilized with an anti-BSA antibody and blocked with human serum albumin. The two conjugates were encapsulated in different pads, respectively. A scheme of the LFA system is described in the part A of first figure. The size of the two conjugates was very critical in the detection sensitivity of troponin I. When 10nm for the 1st and 40 nm for the 2nd were used, the detection sensitivity increased about a 100-fold compared to the conventional LFA. We could detect as low as 0.01 ng/mL troponin I in 10 min using the dual AuNP conjugate-based LFA, which was successfully applied in the analysis of serum samples of patients with myocardial infarction.

摘要

为了在金纳米颗粒(AuNP)侧向流动分析(LFA)中无需额外操作步骤即可实现信号放大,开发了一种新的简单方法,该方法利用了两种 AuNP-抗体缀合物。第一种缀合物是固定有抗肌钙蛋白 I 抗体并用牛血清白蛋白(BSA)封闭的 AuNP,第二种缀合物是固定有抗 BSA 抗体并用人血清白蛋白封闭的 AuNP。这两种缀合物分别包被在不同的垫中。在第一个图的 A 部分中描述了 LFA 系统的示意图。两种缀合物的大小在肌钙蛋白 I 的检测灵敏度中非常关键。当使用 10nm 的第一种和 40nm 的第二种时,与常规 LFA 相比,检测灵敏度提高了约 100 倍。我们使用基于双 AuNP 缀合物的 LFA 可检测低至 0.01ng/mL 的肌钙蛋白 I,该方法已成功应用于心肌梗死患者血清样本的分析。

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