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PNAS Plus: Paper-based microfluidics for DNA diagnostics of malaria in low resource underserved rural communities

机译:PNAS Plus:纸质微流控技术用于在资源匮乏服务水平低下的农村社区进行疟疾的DNA诊断

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摘要

Rapid, low-cost, species-specific diagnosis, based upon DNA testing, is becoming important in the treatment of patients with infectious diseases. Here, we demonstrate an innovation that uses origami to enable multiplexed, sensitive assays that rival polymerase chain reactions (PCR) laboratory assays and provide high-quality, fast precision diagnostics for malaria. The paper-based microfluidic technology proposed here combines vertical flow sample-processing steps, including paper folding for whole-blood sample preparation, with an isothermal amplification and a lateral flow detection, incorporating a simple visualization system. Studies were performed in village schools in Uganda with individual diagnoses being completed in <50 min (faster than the standard laboratory-based PCR). The tests, which enabled the diagnosis of malaria species in patients from a finger prick of whole blood, were both highly sensitive and specific, detecting malaria in 98% of infected individuals in a double-blind first-in-human study. Our method was more sensitive than other field-based, benchmark techniques, including optical microscopy and industry standard rapid immunodiagnostic tests, both performed by experienced local healthcare teams (which detected malaria in 86% and 83% of cases, respectively). All assays were independently validated using a real-time double-blinded reference PCR assay. We not only demonstrate that advanced, low-cost DNA-based sensors can be implemented in underserved communities at the point of need but also highlight the challenges associated with developing and implementing new diagnostic technologies in the field, without access to laboratories or infrastructure.
机译:基于DNA测试的快速,低成本,特定物种诊断在治疗传染病患者中变得越来越重要。在这里,我们展示了一项创新技术,该技术利用折纸技术可以实现与聚合酶链反应(PCR)实验室检测法相媲美的多重敏感检测方法,并为疟疾提供高质量,快速精确的诊断。本文提出的基于纸的微流体技术将垂直流动的样品处理步骤(包括用于全血样品制备的纸张折叠)与等温放大和横向流动检测相结合,并结合了简单的可视化系统。研究在乌干达的乡村学校进行,单个诊断在不到50分钟的时间内完成(比基于实验室的标准PCR更快)。该测试能够通过手指全血来诊断患者的疟疾种类,既具有高度敏感性又具有特异性,在一项双盲首次人体研究中可检测出98%感染者的疟疾。我们的方法比其他基于现场的基准技术(包括光学显微镜和行业标准的快速免疫诊断测试)更加敏感,这两种方法均由经验丰富的本地医疗团队进行(分别在86%和83%的病例中检测到疟疾)。所有检测均使用实时双盲参考PCR检测独立验证。我们不仅证明先进的,低成本的基于DNA的传感器可以在需要时在服务水平低下的社区中实施,还着重指出了在不使用实验室或基础设施的情况下,与开发和实施新诊断技术相关的挑战。

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