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半定量核酸同时等速电泳提取扩增检测

Semiquantitative Nucleic Acid Test with Simultaneous Isotachophoretic Extraction and Amplification.

机构信息

Mechanical Engineering , University of Washington , Seattle , Washington 98195 , United States.

Chemical Engineering , University of Washington , Seattle , Washington 98195 , United States.

出版信息

Anal Chem. 2018 Jun 19;90(12):7221-7229. doi: 10.1021/acs.analchem.8b00185. Epub 2018 May 25.

Abstract

Nucleic acid amplification tests (NAATs) provide high diagnostic accuracy for infectious diseases and quantitative results for monitoring viral infections. The majority of NAATs require complex equipment, cold chain dependent reagents, and skilled technicians to perform the tests. This largely confines NAATs to centralized laboratories and can significantly delay appropriate patient care. Low-cost, point-of-care (POC) NAATs are especially needed in low-resource settings to provide patients with diagnosis and treatment planning in a single visit to improve patient care. In this work, we present a rapid POC NAAT with integrated sample preparation and amplification using electrokinetics and paper substrates. We use simultaneous isotachophoresis (ITP) and recombinase polymerase amplification (RPA) to rapidly extract, amplify, and detect target nucleic acids from serum and whole blood in a paper-based format. We demonstrate simultaneous ITP and RPA can consistently detect 5 copies per reaction in buffer and 10 000 copies per milliliter of human serum with no intermediate user steps. We also show preliminary extraction and amplification of DNA from whole blood samples. Our test is rapid (results in less than 20 min) and made from low-cost materials, indicating its potential for detecting infectious diseases and monitoring viral infections at the POC in low resource settings.

摘要

核酸扩增检测(NAATs)为传染病提供了高诊断准确性,并可对病毒感染进行定量监测。大多数 NAAT 需要复杂的设备、依赖冷链的试剂以及熟练的技术人员来进行检测。这在很大程度上将 NAAT 限制在集中式实验室中,并可能显著延迟对患者的适当护理。在资源匮乏的环境中,尤其需要低成本、即时检测(POC)的 NAAT,以便在单次就诊中为患者提供诊断和治疗计划,从而改善患者护理。在这项工作中,我们提出了一种使用电泳和纸基的快速 POC NAAT,集成了样品制备和扩增。我们使用同时等速电泳(ITP)和重组酶聚合酶扩增(RPA),在纸基格式中从血清和全血中快速提取、扩增和检测目标核酸。我们证明,同时的 ITP 和 RPA 可以在缓冲液中一致地检测到每个反应 5 个拷贝,在人类血清中检测到 10000 个拷贝,无需中间用户步骤。我们还展示了从全血样本中初步提取和扩增 DNA。我们的测试快速(不到 20 分钟即可得出结果),且由低成本材料制成,这表明它有潜力在资源匮乏的环境中用于 POC 检测传染病和监测病毒感染。

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