An integrated lateral flow assay for effective DNA amplification and detection at the point of care

被引:80
作者
Choi, Jane Ru [1 ,2 ,3 ]
Hu, Jie [2 ,3 ]
Gong, Yan [2 ,3 ]
Feng, Shangsheng [3 ,4 ,5 ]
Abas, Wan Abu Bakar Wan [1 ]
Pingguan-Murphy, Belinda [1 ]
Xu, Feng [2 ,3 ]
机构
[1] Univ Malaya, Fac Engn, Dept Biomed Engn, Kuala Lumpur 50603, Malaysia
[2] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Minist Educ, Key Lab Biomed Informat Engn, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, BEBC, Xian 710049, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Aerosp, MOE Key Lab Multifunct Mat & Struct LMMS, Xian 710049, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Aerosp, State Key Lab Mech Struct Strength & Vibrat, Xian 710049, Peoples R China
基金
对外科技合作项目(国际科技项目);
关键词
MEDIATED ISOTHERMAL AMPLIFICATION; LINKED-IMMUNOSORBENT-ASSAY; DENGUE VIRUS; SENSITIVE DETECTION; LABORATORY DIAGNOSIS; IMMUNOGLOBULIN-M; PAPER; PLATFORM; BIOLOGY; FUTURE;
D O I
10.1039/c5an02532j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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 x 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.
引用
收藏
页码:2930 / 2939
页数:10
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