SERS-Based Pump-Free Microfluidic Chip for Highly Sensitive Immunoassay of Prostate-Specific Antigen Biomarkers

被引:105
作者
Gao, Rongke [1 ]
Lv, Zeyuan [1 ]
Mao, Yuanshuo [1 ]
Yu, Liandong [1 ]
Bi, Xiaobai [1 ]
Xu, Shenghao [3 ]
Cui, Jiewu [2 ]
Wu, Yucheng [2 ]
机构
[1] Hefei Univ Technol, Sch Instrument Sci & Optoelect Engn, Hefei 230009, Anhui, Peoples R China
[2] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China
[3] Qingdao Univ Sci & Technol, Shandong Key Lab Biochem Anal, Coll Chem & Mol Engn, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
prostate cancer; pump free microfluidics; SERS; immunoassay; prostate-specific antigen; CANCER; SPECTROSCOPY; PLATFORM; MARKER; SYSTEM; PSA;
D O I
10.1021/acssensors.9b00039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly sensitive analysis of cancer biomarkers demonstrates an important impact in early diagnosis and therapies of cancer. A novel surface-enhanced Raman scattering (SERS) based immunoassay using microfluidic technique was reported for rapid analysis of prostate-specific antigen (PSA) biomarker. It is a useful screening test to discriminate prostate cancer and other diseases related to prostate. A "sandwich" immunoassay based on SERS nanotags, PSA biomarkers, and magnetic beads was applied on a pump-free microfluidic sensor. Magnetic immunocomplexes are isolated and trapped at the detection chamber by a permanent magnet integrated into the chip. The PBS buffer washed magnetic immunocomplexes and brought the free gold nanoparticles to the downsteam channel for waste. Our results show a good linear response in the range from 0.01 to 100 ng mL(-1). The limit of detection of the PSA level is estimated to be below 0.01 ng mL(-1) using this chip. This detection level of PSA biomarker in human serum can be accomplished in 5 min without manual incubation and a heavy syringe pump. To the best of our knowledge, this is the first SERS-based immunoassay which applied a pump-free microfluidic chip as a detection platform. We believe that the proposed method reveals a valuable potential tool for the diagnosis of prostate cancer.
引用
收藏
页码:938 / 943
页数:11
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