环介导等温扩增
注意事项
DNA
点(几何)
等温过程
检测点注意事项
化学
色谱法
计算生物学
生物
医学
物理
生物化学
病理
数学
热力学
几何学
作者
Jane Ru Choi,Jie Hu,Yan Gong,Shangsheng Feng,Wan Abu Bakar Wan Abas,Belinda Pingguan‐Murphy,Feng Xu
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2016-01-01
卷期号:141 (10): 2930-2939
被引量:90
摘要
Lateral flow assays (LFAs) have been extensively explored in nucleic acid testing (NAT) for medical diagnostics, food safety analysis and environmental monitoring. However, the amount of target nucleic acid in a raw sample is usually too low to be directly detected by LFAs, necessitating the process of amplification. Even though cost-effective paper-based amplification techniques have been introduced, they have always been separately performed from LFAs, hence increasing the risk of reagent loss and cross-contaminations. To date, integrating paper-based nucleic acid amplification into colorimetric LFA in a simple, portable and cost-effective manner has not been introduced. Herein, we developed an integrated LFA with the aid of a specially designed handheld battery-powered system for effective amplification and detection of targets in resource-poor settings. Interestingly, using the integrated paper-based loop-mediated isothermal amplification (LAMP)-LFA, we successfully performed highly sensitive and specific target detection, achieving a detection limit of as low as 3 × 10(3) copies of target DNA, which is comparable to the conventional tube-based LAMP-LFA in an unintegrated format. The device may serve in conjunction with a simple paper-based sample preparation to create a fully integrated paper-based sample-to-answer diagnostic device for point-of-care testing (POCT) in the near future.
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