An optimised electrochemical biosensor for the label-free detection of C-reactive protein in blood

被引:183
作者
Bryan, Thomas [1 ]
Luo, Xiliang [1 ,2 ]
Bueno, Paulo R. [3 ]
Davis, Jason J. [1 ]
机构
[1] Univ Oxford, Dept Chem, Oxford OX1 3QZ, England
[2] Qingdao Univ Sci & Technol, Key Lab Biochem Anal, Minist Educ, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[3] Univ Estadual Paulista, Inst Quim, BR-14800900 Sao Paulo, Brazil
关键词
C-reactive protein; Electrochemical impedance spectroscopy; Resistance; Biosensor; Self-assembly; Blood; SELF-ASSEMBLED MONOLAYERS; EPIDEMIOLOGIC APPLICATIONS; IMPEDANCE SPECTROSCOPY; CARDIOVASCULAR-DISEASE; IMMUNOSENSOR DETECTION; CRP DETECTION; HUMAN SERUM; SURFACE; GOLD; ELECTRODES;
D O I
10.1016/j.bios.2012.06.051
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
C-reactive protein (CRP) is an acute phase protein whose levels are increased in many disorders. There exists, in particular, a great deal of interest in the correlation between blood serum levels and the severity of risk for cardiovascular disease. A sensitive, label-free, non-amplified and reusable electrochemical impedimetric biosensor for the detection of CRP in blood serum was developed herein based on controlled and coverage optimised antibody immobilization on standard polycrystalline gold electrodes. Charge transfer resistance changes were highly target specific, linear with log CRP concentration across a 0.5-50 nM range and associated with a limit of detection of 176 pM. Significantly, the detection limits are better than those of current CRP clinical methods and the assays are potentially cheap, relatively automated, reusable, multiplexed and highly portable. The generated interfaces were capable not only of comfortably quantifying CRP across a clinically relevant range of concentrations but also of doing this in whole blood serum with interfaces that were, subsequently, reusable. The importance of optimising receptor layer resistance in maximising assay sensitivity is also detailed. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 98
页数:5
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