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冠状病毒核酸检测的最新进展与展望

Recent advances and perspectives of nucleic acid detection for coronavirus.

作者信息

Shen Minzhe, Zhou Ying, Ye Jiawei, Abdullah Al-Maskri Abdu Ahmed, Kang Yu, Zeng Su, Cai Sheng

机构信息

Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang, 310058, China.

出版信息

J Pharm Anal. 2020 Apr;10(2):97-101. doi: 10.1016/j.jpha.2020.02.010. Epub 2020 Mar 1.

Abstract

The recent pneumonia outbreak caused by a novel coronavirus (SARS-CoV-2) is posing a great threat to global public health. Therefore, rapid and accurate identification of pathogenic viruses plays a vital role in selecting appropriate treatments, saving people's lives and preventing epidemics. It is important to establish a quick standard diagnostic test for the detection of the infectious disease (COVID-19) to prevent subsequent secondary spread. Polymerase chain reaction (PCR) is regarded as a gold standard test for the molecular diagnosis of viral and bacterial infections with high sensitivity and specificity. Isothermal nucleic acid amplification is considered to be a highly promising candidate method due to its fundamental advantage in quick procedure time at constant temperature without thermocycler operation. A variety of improved or new approaches also have been developed. This review summarizes the currently available detection methods for coronavirus nucleic acid. It is anticipated that this will assist researchers and clinicians in developing better techniques for timely and effective detection of coronavirus infection.

摘要

由新型冠状病毒(SARS-CoV-2)引发的近期肺炎疫情正对全球公共卫生构成巨大威胁。因此,快速准确地识别致病病毒对于选择合适的治疗方法、挽救生命以及预防疫情至关重要。建立一种快速的标准诊断测试以检测传染病(COVID-19)对于防止后续二次传播很重要。聚合酶链反应(PCR)被视为用于病毒和细菌感染分子诊断的金标准测试,具有高灵敏度和特异性。等温核酸扩增由于其在恒温下无需热循环仪操作即可快速完成程序的根本优势,被认为是一种极具前景的候选方法。各种改进的或新的方法也已被开发出来。本综述总结了目前可用的冠状病毒核酸检测方法。预计这将有助于研究人员和临床医生开发更好的技术,以便及时有效地检测冠状病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae71/7192971/eb2a0c7ba52c/fx1.jpg

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