A microfluidic system for rapid nucleic acid analysis based on real-time convective PCR at point-of-care testing

被引:14
|
作者
Xu, Donglin [1 ]
Jiang, Xiaodan [1 ]
Zou, Tianli [2 ]
Miao, Guijun [1 ]
Fu, Qiang [1 ]
Xiang, Fei [1 ]
Feng, Liang [1 ]
Ye, Xiangzhong [2 ]
Zhang, Lulu [1 ]
Qiu, Xianbo [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Informat Sci & Technol, Inst Microfluid Chip Dev Biomed Engn, Beijing 100029, Peoples R China
[2] Beijing Wantai Biol Pharm Enterprise Co Ltd, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
Microfluidic chip; Nucleic acid analysis; Mixing; Nucleic acid extraction; Convective PCR; Point-of-care (POC) testing; ON-A-CHIP; MOLECULAR DIAGNOSIS; AMPLIFICATION;
D O I
10.1007/s10404-022-02577-5
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A microfluidic system for rapid nucleic acid analysis based on real-time convective PCR is developed. To perform 'sample-in, answer-out' nucleic acid analysis, a microfluidic chip is developed to efficiently extract nucleic acid, and meanwhile convective PCR (CPCR) is applied for rapid nucleic acid amplification. With an integrated microfluidic chip consisting of reagent pre-storage chambers, a lysis & wash chamber, an elution chamber and a waste chamber, nucleic acid extraction based on magnetic beads can be automatically performed for a large size of test sample within a limited time. Based on an easy-to-operate strategy, different pre-stored reagents can be conveniently released for consecutive reaction at different steps. To achieve efficient mixing, a portable companion device is developed to introduce properly controlled 3-D actuation to magnetic beads in nucleic acid extraction. In CPCR amplification, PCR reagent can be spontaneously and repeatedly circulated between hot and cool zones of the reactor for space-domain thermal cycling based on pseudo-isothermal heating. A handheld real-time CPCR device is developed to perform nucleic acid amplification and in-situ detection. To extend the detection throughput, multiple handheld real-time CPCR devices can be grouped together by a common control system. It is demonstrated that influenza A (H1N1) viruses with the reasonable concentration down to 1.0 TCID50/ml can be successfully detected with the microfluidic system.
引用
收藏
页数:9
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