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Ni(II)NTA AuNPs 作为一种低资源疟疾诊断平台,用于快速比色检测恶性疟原虫富组氨酸蛋白 2。

Ni(II)NTA AuNPs as a low-resource malarial diagnostic platform for the rapid colorimetric detection of Plasmodium falciparum Histidine-Rich Protein-2.

机构信息

Department of Chemistry, Vanderbilt University, Station B 351822-1822, Nashville, TN 37235-1822, United States.

Department of Chemistry, Vanderbilt University, Station B 351822-1822, Nashville, TN 37235-1822, United States.

出版信息

Talanta. 2015 Apr;135:94-101. doi: 10.1016/j.talanta.2014.12.047. Epub 2015 Jan 7.

Abstract

Diagnosing infectious diseases remains a challenge in the developing world where there is a lack of dependable electricity, running water, and skilled technicians. Although rapid immunochromatographic tests (RDTs) have been deployed to diagnose diseases such as malaria, the extreme climate conditions encountered in these regions compounded with the discrepancies in test manufacturing have yielded varying results, so that more innovative and robust technologies are sought. Devoid of antibodies and thermally sensitive materials, we present a robust, colorimetric diagnostic platform for the detection of a malarial biomarker, Plasmodium falciparum Histidine-Rich Protein 2 (PfHRP-II). The assay exploits the optical properties of gold nanoparticles, covalently coupling them to a Ni(II)NTA recognition element specific for PfHRP-II. In the presence of the recombinant malarial biomarker (rcHRP-II), the Ni(II)NTA AuNPs begin to crosslink and aggregate in as little as one minute, triggering a red-to-purple color change in solution. To increase assay sensitivity and platform stability suitable for low-resource regions, the Ni(II)NTA AuNPs were assembled with varying spacer ligands in a mixed monolayer presentation. When assembled with a negatively charged Peg4-thiol ligand, the Ni(II)NTA AuNPs demonstrate low nanomolar limits of rcHRP-II detection in physiological concentrations of human serum albumin and maintain excellent stability at 37°C when stored for four weeks. Detection of the malaria biomarker is also measured by capturing and processing images of aggregated gold nanoparticles with a smartphone camera. By utilizing a smartphone camera and image processing application, there is no significant difference in assay sensitivity and rcHRP-II limit of detection in comparison to a spectrophotometer, further making this diagnostic platform applicable for use in low-resource regions.

摘要

在发展中国家,由于缺乏可靠的电力、自来水和熟练的技术人员,诊断传染病仍然是一个挑战。虽然已经部署了快速免疫层析检测(RDT)来诊断疟疾等疾病,但这些地区遇到的极端气候条件以及测试制造的差异导致了不同的结果,因此需要寻求更具创新性和更强健的技术。由于缺乏抗体和对热敏感的材料,我们提出了一种稳健的比色诊断平台,用于检测疟原生物标志物恶性疟原虫富组氨酸蛋白 2(PfHRP-II)。该测定法利用了金纳米粒子的光学性质,将其共价偶联到特异性识别 PfHRP-II 的 Ni(II)NTA 识别元件上。在存在重组疟原生物标志物(rcHRP-II)的情况下,Ni(II)NTA AuNPs 开始在短短一分钟内交联和聚集,引发溶液中颜色从红色变为紫色。为了提高 assay 灵敏度和平台稳定性,使其适用于资源匮乏的地区,将 Ni(II)NTA AuNPs 与不同的间隔配体组装在混合单层中。当与带负电荷的 Peg4-硫醇配体组装时,Ni(II)NTA AuNPs 在生理浓度的人血清白蛋白中表现出对 rcHRP-II 的低纳摩尔检测限,并在 37°C 下储存四周时保持出色的稳定性。还可以通过智能手机摄像头捕获和处理聚集的金纳米粒子的图像来测量疟疾生物标志物的检测。通过利用智能手机摄像头和图像处理应用程序,与分光光度计相比,assay 灵敏度和 rcHRP-II 的检测限没有明显差异,进一步使该诊断平台适用于资源匮乏的地区。

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