Smartphone-imaged multilayered paper-based analytical device for colorimetric analysis of carcinoembryonic antigen

被引:58
作者
Wang, Kan [1 ]
Yang, Jinchuan [1 ]
Xu, Hao [2 ]
Cao, Bo [1 ]
Qin, Qi [1 ]
Liao, Xinmei [1 ]
Wo, Yan [3 ]
Jin, Qinghui [4 ,5 ]
Cui, Daxiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Engn Res Ctr Intelligent Diag & Treatmen, Dept Instrument Sci & Engn,Sch Elect Informat & E, Key Lab Thin Film & Microfabricat,Ministry Educ, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Naval Architecture Ocean & Civil Engn, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Plast & Reconstruct Surg, Shanghai 200011, Peoples R China
[4] Chinese Acad Sci, State Key Lab Transducer Technol, Shanghai Inst Microsyst & Informat Technol, Shanghai 200050, Peoples R China
[5] Ningbo Univ, Fac Elect Engn & Comp Sci, Ningbo 315211, Peoples R China
基金
中国国家自然科学基金;
关键词
Microfluidic paper-based analytical device (mu PAD); Carcinoembryonic antigen (CEA); Smartphone; Point-of-care testing (POCT); GASTRIC-CANCER PATIENTS; TUMOR-MARKER; SENSITIVE DETECTION; LOW-COST; IMMUNOCHROMATOGRAPHIC ASSAY; QUANTITATIVE DETECTION; IMMUNOSORBENT-ASSAY; RAPID DETECTION; IMMUNOASSAY; FABRICATION;
D O I
10.1007/s00216-020-02475-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Paper-based immunoassays are effective methods that employ microfluidic paper-based analytical devices (mu PADs) for the rapid, simple, and accurate quantification of analytes in point-of-care diagnosis. In this study, we developed a wax-printed multilayered mu PAD for the colorimetric detection of carcinoembryonic antigen (CEA), where the device contained a movable and rotatable detection layer to allow the mu PAD to switch the state of the sample solutions, i.e., flowing or storing in the sensing zones. A smartphone with a custom-developed program served as an automated colorimetric reader to capture and analyze images from the mu PAD, before calculating and displaying the test results. After optimizing the crucial conditions for the assay, the proposed method exhibited a wide linear dynamic range from 0.5 to 70 ng/mL, with a low CEA detection limit of 0.015 ng/mL. The clinical performance of this method was successfully validated using 50 positive and 40 negative human serum samples, thereby demonstrating the high sensitivity of 98.0% and specificity of 97.5% in the detection of CEA. The proposed method is greatly simplified compared with the cumbersome steps required for traditional immunoassays, but without any loss of accuracy and stability, as well as reducing the time needed to detect CEA. Complex and bulky instruments are replaced with a smartphone. The proposed detection platform could potentially be applied in point-of-care testing. Graphical abstract
引用
收藏
页码:2517 / 2528
页数:12
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