A microfluidic immunoassay platform for the detection of free prostate specific antigen: a systematic and quantitative approach

被引:20
作者
Madaboosi, Narayanan [1 ,2 ]
Soares, Ruben R. G. [1 ,2 ,3 ]
Chu, Virginia [1 ,2 ]
Conde, Joao Pedro [1 ,2 ,4 ]
机构
[1] INESC Microsistemas & Nanotecnol, Lisbon, Portugal
[2] IN Inst Nanosci & Nanotechnol, Lisbon, Portugal
[3] Univ Lisbon, Inst Super Tecn, iBB Inst Bioengn & Biosci, P-1699 Lisbon, Portugal
[4] Univ Lisbon, Inst Super Tecn, Dept Bioengn, P-1699 Lisbon, Portugal
关键词
FREE PSA; ULTRASENSITIVE DETECTION; CANCER; BIOMARKERS; FLUORESCENCE; ORIENTATION; DESIGN; FUTURE; ELISA; SERUM;
D O I
10.1039/c5an00364d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
As a leading cause of cancer-related deaths in men globally, prostate cancer (PCa) demands immense attention for theranostic purposes. There is an increasing need for the development of rapid, sensitive, economical, miniaturized and multiplexable assays. Towards this goal, we present a systematic approach for the optimisation of a microfluidic sandwich immunoassay, which can be applied as a generic biosensor platform for PCa detection. Prostate specific antigen (PSA) was used as the model biomarker, and its free form was captured using commercially available antibodies and detected using chemiluminescence, both in spiked buffer and matrix solutions. Along with the optimisation of surface chemistry and microfluidic parameters, we report a bio-affinity amplification strategy based on biotin-streptavidin chemistry to bring the limits of detection for free-PSA from 21.4 ng mL(-1) down to 2.7 ng mL(-1), within the clinically relevant range. An estimate of the surface coverage and simulations of the interactions taking place in the microfluidic biosensor during the assay are also presented. This novel platform using a simple passive adsorption-based bio-affinity strategy, when coupled with multiplexing and integrated detection, can serve as a promising point-of-care diagnostic tool for PCa.
引用
收藏
页码:4423 / 4433
页数:11
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