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金纳米粒子-侧向流免疫分析,一种检测尿液华支睾吸虫(Ov)抗原的有效方法。

AuNPs-LISA, an efficient detection assay for Opisthorchis viverrini (Ov) antigen in urine.

机构信息

Department of Biochemistry, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.

出版信息

Talanta. 2020 Mar 1;209:120592. doi: 10.1016/j.talanta.2019.120592. Epub 2019 Nov 27.

Abstract

The enzyme-linked immunosorbent assay (ELISA) is currently a powerful technique for the detection of Opisthorchis viverrini antigen (OvAg) in urine samples. However, its sensitivity and analysis time need to be improved. In the present study, we aimed to improve the signal enhancing system of traditional ELISA by using gold nanoparticles (AuNPs) with peroxidase-like activity on its surface instead of the horseradish peroxidase (HRP) system. The catalytic activity of the AuNPs probe can be boosted by the gold enhancing solution and the addition of ATP. The catalytic ability of the AuNPs probe depended on the probe and the HO concentration. The proposed approach can reduce the number of the traditional ELISA steps with better detection sensitivity. Interestingly, the limit of detection (LOD) of the test was 23.4 ng mL, substantially lower than the 93.8 ng mL for the traditional ELISA. The AuNPs-LISA assay showed higher sensitivity and specificity, 93.81% and 91.34%, respectively, compared to the traditional ELISA. The proposed assay was successfully applied for the detection of OvAg in urine samples. This will provide an effective tool for the detection, control and elimination of human opisthorchiasis.

摘要

酶联免疫吸附测定(ELISA)目前是一种检测华支睾吸虫抗原(OvAg)在尿液样本中的强大技术。然而,其灵敏度和分析时间需要改进。在本研究中,我们旨在通过使用表面具有过氧化物酶样活性的金纳米粒子(AuNPs)代替辣根过氧化物酶(HRP)系统来改进传统 ELISA 的信号增强系统。金增强溶液和添加的 ATP 可以增强 AuNPs 探针的催化活性。AuNPs 探针的催化能力取决于探针和 HO 浓度。该方法可以减少传统 ELISA 步骤的数量,并具有更好的检测灵敏度。有趣的是,该测试的检测限(LOD)为 23.4ng/mL,明显低于传统 ELISA 的 93.8ng/mL。与传统 ELISA 相比,AuNPs-LISA 检测法的灵敏度和特异性分别为 93.81%和 91.34%。该检测方法成功应用于尿液样本中 OvAg 的检测。这将为华支睾吸虫病的检测、控制和消除提供有效的工具。

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