化学
微流控
核酸
口腔黏膜测试
条形码
多路复用
流体学
色谱法
环介导等温扩增
多路复用
核酸酶
逆转录酶
DNA
固相萃取
DNA提取
纳斯巴
聚合酶链反应
检出限
样品制备
纳米技术
计算机科学
生物化学
分子生物学
操作系统
电信
基因
核酸序列
航空航天工程
生物
工程类
材料科学
生物信息学
作者
Leah M. Dignan,M. Shane Woolf,Christopher J. Tomley,Aeren Q. Nauman,James P. Landers
标识
DOI:10.1021/acs.analchem.1c00842
摘要
This report describes the development of a centrifugally controlled microfluidic dynamic solid-phase extraction (dSPE) platform to reliably obtain amplification-ready nucleic acids (NAs) directly from buccal swab cuttings. To our knowledge, this work represents the first centrifugal microdevice for comprehensive preparation of high-purity NAs from raw buccal swab samples. Direct-from-swab cellular lysis was integrated upstream of NA extraction, and automatable laser-controlled on-board microvalving strategies provided the strict spatiotemporal fluidic control required for practical point-of-need use. Solid-phase manipulation during extraction leveraged the application of a bidirectional rotating magnetic field to promote thorough interaction with the sample (e.g., NA capture). We illustrate the broad utility of this technology by establishing downstream compatibility of extracted nucleic acids with three noteworthy assays, namely, the polymerase chain reaction (PCR), reverse transcriptase PCR (RT-qPCR), and loop-mediated isothermal amplification (LAMP). The PCR-readiness of the extracted DNA was confirmed by generating short tandem repeat (STR) profiles following multiplexed amplification. With no changes to assay workflow, viral RNA was successfully extracted from contrived (spiked) SARS-CoV-2 swab samples, confirmed by RT-qPCR. Finally, we demonstrate the compatibility of the extracted DNA with LAMP-a technique well suited for point-of-need genetic analysis due to minimal hardware requirements and compatibility with colorimetric readout. We describe an automatable, portable microfluidic platform for the nucleic acid preparation device that could permit practical, in situ use by nontechnical personnel.
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