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一种使用自然对流并结合智能手机的便携式核酸检测系统。

A portable nucleic acid detection system using natural convection combined with a smartphone.

机构信息

Department of Molecular Sciences, Macquarie University, Sydney, Australia.

School of Chemistry and Australian Centre for Nanomedicine, University of New South Wales, Sydney, Australia.

出版信息

Biosens Bioelectron. 2019 Jun 1;134:68-75. doi: 10.1016/j.bios.2019.03.050. Epub 2019 Mar 29.

Abstract

The development of portable nucleic acid diagnostic devices has the potential to expand the availability of molecular diagnostics into low-resource settings. One of the promising solutions for rapid and simple DNA amplification is the use of Rayleigh-Bernard natural convection which is caused by a buoyancy-driven thermal gradient of liquid when heated from below. This natural convection avoids the use of the complex and sophisticated hardware that is required for precise maintenance of temperature cycles in conventional PCR. We have developed a stand-alone convective PCR (cPCR) device linked to a smartphone for rapid detection of nucleic acids using natural convection heating. The device amplifies multiple DNA samples simultaneously using a custom-made heat block controlled by Bluetooth wireless communication. The entire device is highly portable, user-friendly, battery-operated and can provide target DNA amplification in less than 30 min. A detection limit of 2.8 × 10 copies of a segment of lambda DNA was obtained when the two different fluorescently-tagged amplicons were collected magnetically and detected using the smartphone fluorescence reader. Thus, the combination of cPCR and multiplex fluorescence-based detection on a smartphone provides new opportunities for the development of affordable and portable molecular diagnostic devices for point-of-care situations or remote clinical settings.

摘要

便携式核酸诊断设备的发展有可能将分子诊断技术扩展到资源匮乏的环境中。一种快速、简单的 DNA 扩增方法是利用瑞利-贝纳德自然对流,当液体从底部加热时,会产生由浮力驱动的热梯度。这种自然对流避免了传统 PCR 中需要复杂而精密的硬件来精确维持温度循环。我们已经开发了一种独立的基于自然对流加热的智能手机连接式对流聚合酶链反应(cPCR)设备,用于快速检测核酸。该设备使用蓝牙无线通信控制的定制加热块同时扩增多个 DNA 样本。整个设备高度便携、用户友好、电池供电,可在不到 30 分钟内提供目标 DNA 扩增。当使用智能手机荧光读取器收集并检测两种不同荧光标记的扩增子时,获得了 2.8×10 个 lambda DNA 片段的检测限。因此,cPCR 与智能手机上的基于多重荧光的检测相结合,为开发经济实惠且便携的分子诊断设备,以用于即时护理或远程临床环境提供了新的机会。

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