An integrated paper-based sample-to-answer biosensor for nucleic acid testing at the point of care

被引:243
作者
Choi, Jane Ru [1 ,2 ,3 ]
Hu, Jie [1 ,3 ]
Tang, Ruihua [1 ,3 ,4 ]
Gong, Yan [1 ,3 ]
Feng, Shangsheng [3 ,5 ,6 ]
Ren, Hui [3 ,7 ,8 ]
Wen, Ting
Li, XiuJun [9 ,10 ,11 ]
Abas, Wan Abu Bakar Wan [2 ]
Pingguan-Murphy, Belinda [2 ]
Xu, Feng [1 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Minist Educ, Key Lab Biomed Informat Engn, Xian 710049, Peoples R China
[2] Univ Malaya, Fac Engn, Dept Biomed Engn, Kuala Lumpur 50603, Malaysia
[3] Xi An Jiao Tong Univ, BEBC, Xian 710049, Peoples R China
[4] Northwestern Polytech Univ, Key Lab Space Biosci & Biotechnol, Xian 710072, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Aerosp, EMOE Key Lab Multifunct Mat & Struct LMMS, Xian 710049, Peoples R China
[6] Xi An Jiao Tong Univ, Sch Aerosp, State Key Lab Mech Struct Strength & Vibrat, Xian 710049, Peoples R China
[7] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Resp & Crit Care Med, Xian 710061, Peoples R China
[8] Xian Diandi Biotech Co, Xian 710049, Peoples R China
[9] Univ Texas El Paso, Dept Chem, Coll Hlth Sci, El Paso, TX 79968 USA
[10] Univ Texas El Paso, Biomed Engn, El Paso, TX 79968 USA
[11] Univ Texas El Paso, Border Biomed Res Ctr, El Paso, TX 79968 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
LATERAL FLOW ASSAY; ESCHERICHIA-COLI O157H7; ISOTHERMAL AMPLIFICATION; SENSITIVE DETECTION; DISEASE; BIOLOGY; STRIP;
D O I
10.1039/c5lc01388g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With advances in point-of-care testing (POCT), lateral flow assays (LFAs) have been explored for nucleic acid detection. However, biological samples generally contain complex compositions and low amounts of target nucleic acids, and currently require laborious off-chip nucleic acid extraction and amplification processes (e.g., tube-based extraction and polymerase chain reaction (PCR)) prior to detection. To the best of our knowledge, even though the integration of DNA extraction and amplification into a paper-based biosensor has been reported, a combination of LFA with the aforementioned steps for simple colorimetric readout has not yet been demonstrated. Here, we demonstrate for the first time an integrated paper-based biosensor incorporating nucleic acid extraction, amplification and visual detection or quantification using a smartphone. A handheld battery-powered heating device was specially developed for nucleic acid amplification in POC settings, which is coupled with this simple assay for rapid target detection. The biosensor can successfully detect Escherichia coli (as a model analyte) in spiked drinking water, milk, blood, and spinach with a detection limit of as low as 10-1000 CFU mL(-1), and Streptococcus pneumonia in clinical blood samples, highlighting its potential use in medical diagnostics, food safety analysis and environmental monitoring. As compared to the lengthy conventional assay, which requires more than 5 hours for the entire sample-to-answer process, it takes about 1 hour for our integrated biosensor. The integrated biosensor holds great potential for detection of various target analytes for wide applications in the near future.
引用
收藏
页码:611 / 621
页数:11
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