Protein-responsive polymers for point-of-care detection of cardiac biomarker

被引:80
作者
Moreira, Felismina T. C. [1 ,2 ,3 ]
Sharma, Sanjiv [4 ,5 ]
Dutra, Rosa A. F. [6 ]
Noronha, Joao P. C. [3 ]
Cass, Anthony E. G. [4 ,5 ]
Sales, M. Goreti F. [1 ]
机构
[1] Polytech Inst Porto, BioMark ISEP, Sch Engn, Oporto, Portugal
[2] INESC TEC, Oporto, Portugal
[3] Univ Nova Lisboa, REQUIMTE FCT UNL, Fac Ciencias & Tecnol, P-1200 Lisbon, Portugal
[4] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AY, England
[5] Univ London Imperial Coll Sci Technol & Med, Inst Biomed Engn, London, England
[6] Univ Fed Pernambuco, PROCAPE, LAPED, Recife, PE, Brazil
基金
英国工程与自然科学研究理事会;
关键词
Biomimetic antibodies; Screen-printed electrodes; Molecular imprinting; Electropolymerization; Myoglobin; Biosensor; MOLECULARLY IMPRINTED POLYMERS; ACUTE MYOCARDIAL-INFARCTION; PERFORMANCE LIQUID-CHROMATOGRAPHY; SCREEN-PRINTED ELECTRODES; MYOGLOBIN DETECTION; SURFACE; RECOGNITION; AMINOPHENOL; SENSOR; DIAGNOSIS;
D O I
10.1016/j.snb.2014.01.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work describes a novel use for the polymeric film, poly( o-aminophenol) (PAP) that was made responsive to a specific protein. This was achieved through templated electropolymerization of aminophenol (AP) in the presence of protein. The procedure involved adsorbing protein on the electrode surface and thereafter electroploymerizing the aminophenol. Proteins embedded at the outer surface of the polymeric film were digested by proteinase K and then washed away thereby creating vacant sites. The capacity of the template film to specifically rebind protein was tested with myoglobin (Myo), a cardiac biomarker for ischemia. The films acted as biomimetic artificial antibodies and were produced on a gold (Au) screen printed electrode (SPE), as a step towards disposable sensors to enable point-of-care applications. Raman spectroscopy was used to follow the surface modification of the Au-SPE. The ability of the material to rebind Myo was measured by electrochemical techniques, namely electrochemical impedance spectroscopy (EIS) and square wave voltammetry (SWV). The devices displayed linear responses to Myo in EIS and SWV assays down to 4.0 and 3.5 mu g/mL, respectively, with detection limits of 1.5 and 0.8 mu g/mL. Good selectivity was observed in the presence of troponin T (TnT) and creatine kinase (CKMB) in SWV assays, and accurate results were obtained in applications to spiked serum. The sensor described in this work is a potential tool for screening Myo in point-of-care due to the simplicity of fabrication, disposability, short time response, low cost, good sensitivity and selectivity. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
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