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
相关论文
共 48 条
[1]   A lab-in-a-briefcase for rapid prostate specific antigen (PSA) screening from whole blood [J].
Barbosa, Ana I. ;
Castanheira, Ana P. ;
Edwards, Alexander D. ;
Reis, Nuno M. .
LAB ON A CHIP, 2014, 14 (16) :2918-2928
[2]   MOLECULAR-MASS AND CARBOHYDRATE STRUCTURE OF PROSTATE-SPECIFIC ANTIGEN - STUDIES FOR ESTABLISHMENT OF AN INTERNATIONAL PSA STANDARD [J].
BELANGER, A ;
VANHALBEEK, H ;
GRAVES, HCB ;
GRANDBOIS, K ;
STAMEY, TA ;
HUANG, LH ;
POPPE, I ;
LABRIE, F .
PROSTATE, 1995, 27 (04) :187-197
[3]   Mechanisms of self-association of a human monoclonal antibody CNTO607 [J].
Bethea, Deidra ;
Wu, Sheng-Jiun ;
Luo, Jinquan ;
Hyun, Linus ;
Lacy, Eilyn R. ;
Teplyakov, Alexey ;
Jacobs, Steven A. ;
O'Neil, Karyn T. ;
Gilliland, Gary L. ;
Feng, Yiqing .
PROTEIN ENGINEERING DESIGN & SELECTION, 2012, 25 (10) :531-537
[4]  
Bickers B, 2009, ANTICANCER RES, V29, P3289
[5]   Engineering novel binding proteins from nonimmunoglobulin domains [J].
Binz, HK ;
Amstutz, P ;
Plückthun, A .
NATURE BIOTECHNOLOGY, 2005, 23 (10) :1257-1268
[6]   Antibody production, design and use for biosensor-based applications [J].
Conroy, Paul J. ;
Hearty, Stephen ;
Leonard, Paul ;
O'Kennedy, Richard J. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2009, 20 (01) :10-26
[7]   Surface plasmon resonance application in prostate cancer biomarker research [J].
Damborsky, Pavel ;
Madaboosi, Narayanan ;
Chu, Virginia ;
Conde, Joao P. ;
Katrlik, Jaroslav .
CHEMICAL PAPERS, 2015, 69 (01) :143-149
[8]   Perspective: Flicking with flow: Can microfluidics revolutionize the cancer research? [J].
Das, Tamal ;
Chakraborty, Suman .
BIOMICROFLUIDICS, 2013, 7 (01)
[9]   Evaluation of [-2] proPSA and Prostate Health Index (phi) for the detection of prostate cancer: a systematic review and meta-analysis [J].
Filella, Xavier ;
Gimenez, Nuria .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2013, 51 (04) :729-739
[10]  
Garcia-Cordero JL, 2014, LAB CHIP, V14, P2642, DOI [10.1039/C3LC51153G, 10.1039/c3lc51153g]