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从唾液中快速、经济且规模化地检测 SARS-CoV-2。

Rapid, Affordable, and Scalable SARS-CoV-2 Detection From Saliva.

机构信息

Center for Functional Genomics, University at Albany, Rensselaer, New York, USA.

Department of Biomedical Sciences, School of Public Health, University at Albany, Rensselaer, New York, USA.

出版信息

J Biomol Tech. 2021 Sep;32(3):148-157. doi: 10.7171/jbt.21-3203-010.

Abstract

Here we present an inexpensive, rapid, and robust reverse-transcription loop-mediated isothermal amplification (RT-LAMP)-based severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection method that is easily scalable, enabling point-of-care facilities and clinical labs to determine results from patients' saliva directly in 30 minutes for less than $2 per reaction. The method uses a novel combination of widely available reagents that can be prepared in bulk, plated, and frozen and remain stable until samples are received. This innovation dramatically reduces preparation time, enabling high-throughput automation and testing with time to results (including setup) in less than 1 hour for 96 patient samples simultaneously when using a 384-well format. By using a dual reporter (phenol red pH indicator for end-point detection and SYTO-9 fluorescent dye for real time), the assay also provides internal validation of results and redundancy in the event of an instrument malfunction.

摘要

在这里,我们提出了一种廉价、快速且稳健的逆转录环介导等温扩增(RT-LAMP)检测方法,可直接对患者的唾液样本进行现场即时检测,30 分钟内即可出结果,每个反应的成本不到 2 美元。该方法使用了一种新颖的组合试剂,可大量制备、划线、冷冻,在收到样本之前保持稳定。这种创新极大地减少了准备时间,可实现高通量自动化,并在使用 384 孔格式时,将 96 个患者样本的结果(包括设置)时间缩短至 1 小时以内。该检测方法还使用了双报告基因(终点检测用苯酚红 pH 指示剂和实时检测用 SYTO-9 荧光染料),为结果提供了内部验证,并在仪器发生故障时提供了冗余性。

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