清脆的
DNA
数字聚合酶链反应
污染
注意事项
核糖核酸
计算生物学
病毒学
计算机科学
生物
聚合酶链反应
医学
遗传学
基因
生态学
护理部
作者
Sheng Li,Haofan Yin,Jiale Zheng,Yunzhu Wan,Ke Wang,Chongguang Yang,Jianhua Zhou,Meng Zhao,Xiaopeng Yuan,Jiasi Wang
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2024-07-20
卷期号:9 (8): 4256-4264
被引量:1
标识
DOI:10.1021/acssensors.4c01248
摘要
Rapid and precise nucleic acid testing at the point-of-care (POC) is essential for effective screening and management of infectious diseases. Current polymerase-based molecular diagnostics often suffer from potential cross-contamination issues, particularly in POC settings. Here, we introduce DECODE, a contamination-free nucleic acid detection platform integrating digital microfluidics (DMF) for nucleic acid extraction and a digital CRISPR amplification-free assay for pathogen detection. The digital CRISPR assay demonstrates sensitivity, detecting target DNA and RNA in the reaction mixture at concentrations of 10 and 5 copies/μL, respectively. Leveraging DMF-extracted samples enhances the performance of the digital CRISPR amplification-free assay. DECODE offers a sample-to-result workflow of 75 min using compact devices. Validation studies using clinical samples confirm DECODE's robust performance, achieving 100% sensitivity and specificity in detecting HPV18 from cervical epithelial cells and influenza A from nasal swabs. DECODE represents a versatile, contamination-free detection platform poised to enhance integrated public health surveillance efforts.
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