A compact, low-cost, quantitative and multiplexed fluorescence detection platform for point-of-care applications

被引:34
|
作者
Obahiagbon, Uwadiae [1 ]
Smith, Joseph T. [1 ,2 ]
Zhu, Meilin [2 ]
Katchman, Benjamin A. [2 ]
Arafa, Hany [1 ]
Anderson, Karen S. [2 ]
Christen, Jennifer M. Blain [1 ]
机构
[1] Arizona State Univ, Sch Elect Comp & Energy Engn, Goldwater Ctr, Suite 334, Tempe, AZ 85287 USA
[2] Arizona State Univ, Ctr Personalized Diagnost, Biodesign Inst, Tempe, AZ 85281 USA
来源
基金
美国国家科学基金会;
关键词
Point-of-care; Diagnostics; Multiplexed; Fluorescence; Colorimetry; Limit of detection; INTEGRATION; SENSITIVITY; SENSORS;
D O I
10.1016/j.bios.2018.04.002
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An effective method of combating infectious diseases is the deployment of hand-held devices at the point-of-care (POC) for screening or self-monitoring applications. There is a need for very sensitive, low-cost and quantitative diagnostic devices. In this study, we present a low-cost, multiplexed fluorescence detection platform that has a high sensitivity and wide dynamic range. Our system features inexpensive 3 x 3 mm interference filters with a high stopband rejection, sharp transition edges, and greater than 90% transmission in the passband. In addition to the filters, we improve signal-to-noise ratio by leveraging time for accuracy using a charge-integration-based readout. The fluorescence sensing platform provides a sensitivity to photon flux of similar to 1 x 10(4) photons/mm(2) sec and has the potential for 2-3 orders of magnitude improvement in sensitivity over standard colorimetric detection that uses colored latex microspheres. We also detail the design, development, and characterization of our low-cost fluorescence detection platform and demonstrate 100% and 97.96% reduction in crosstalk probability and filter cost, respectively. This is achieved by reducing filter dimensions and ensuring appropriate channel isolation in a 2 x 2 array configuration. Practical considerations with low-cost interference filter system design, analysis, and system performance are also discussed. The performance of our platform is compared to that of a standard laboratory array scanner. We also demonstrate the detection of antibodies to human papillomavirus (HPV16) E7 protein, as a potential biomarker for early cervical cancer detection in human plasma.
引用
收藏
页码:153 / 160
页数:8
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