化学
复式(建筑)
重组酶聚合酶扩增
微流控
DNA
检出限
荧光
聚合酶链反应
工作流程
计算生物学
重组酶
炸薯条
污染
色谱法
灵敏度(控制系统)
纳米技术
杂交探针
生物系统
实时聚合酶链反应
食品安全
放射性检测
信号(编程语言)
STR分析
DNA分析
作者
Hongyan Liu,Junjie Chen,Leshan Xiu,Yang Liu,Ting-Ting Wei,Yue Wang,Liang Shi,Xu Wang,Xiang Li,Kun Yin
标识
DOI:10.1021/acs.analchem.6c02717
摘要
Species fingerprinting is crucial to ensure food safety and human health, which requires a rapid, simple, multiplex, and field-deployable detection technique. In response, a lab-on-a-disc microfluidic chip with CRISPR/Cas12a that integrates target preamplification and signal readout enhanced by tetrahedral DNA frameworks (TDFs) has been developed in this study. This platform automates the workflow from recombinase polymerase amplification (RPA) through signal readout. In addition, a portable heating module was developed specifically for colorimetric detection, providing a complete field-deployable solution. The performance of the CRISPR/Cas12a platform was evaluated by detecting cow's milk adulteration in buffalo milk. The platform demonstrated high sensitivity, achieving detection limits of 1% (v/v) and 5% (v/v) for fluorescence and colorimetric detection within 1 h, respectively. The results agree well with those from real-time quantitative polymerase chain reaction (qPCR) in real-sample analysis. The integrated CRISPR/Cas12a-based duplex detection platform features high sensitivity and specificity, reaction automation, minimal aerosol contamination risk, and decentralized operation, which demonstrates significant potential for field-deployable species fingerprinting and risk prediction.
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