Paper-based (bio)sensor for label-free detection of 3-nitrotyrosine in human urine samples using molecular imprinted polymer

被引:35
|
作者
Martins, Gabriela V. [1 ,2 ,3 ,4 ,5 ]
Marques, Ana C. [1 ,2 ,3 ,4 ]
Fortunato, Elvira [3 ,4 ]
Sales, M. Goreti F. [1 ,2 ,5 ]
机构
[1] Univ Coimbra, Fac Sci & Technol, BioMark UC, Coimbra, Portugal
[2] Polytech Sch, Sch Engn, BioMark ISEP, Porto, Portugal
[3] Univ Nova Lisboa, Fac Sci & Technol, Dept Mat Sci, i3N CENIMAT, Campus Caparica, Setubal, Portugal
[4] Univ Nova Lisboa, CEMOP, Campus Caparica, Setubal, Portugal
[5] Univ Minho, CEB Ctr Biol Engn, P-4710057 Braga, Portugal
基金
欧盟地平线“2020”;
关键词
3-nitrotyrosine; Molecular imprinted polymer; Electrochemical (bio)sensor; Urine biomarker; Carbon-printed electrode; ELECTROCHEMICAL DETECTION; OXIDATIVE STRESS; HUMAN PLASMA; SENSOR; BIOMARKER; ELECTRODES; COMPOSITE; RECEPTOR; DEVICE; 8-HYDROXY-2'-DEOXYGUANOSINE;
D O I
10.1016/j.sbsr.2020.100333
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Over the last years, paper technology has been widely spread as a more affordable, sustainable and reliable support material to be incorporated in the design of point-of-care (POC) diagnostic devices. However, the single work employing a paper-based device for 3-nitrotyrosine (3-NT), a relevant biomarker for oxidative stress (OS) that is a major origin for many diseases, is incapable of reading successfully complex samples because every species that oxidizes before similar to 0.75 V will also contribute to the final response. Thus, the introduction of a selective element was made into this set-up by including a molecularly-imprinted polymer (MIP) tailored in-situ. Herein, a novel MIP for 3-NT was assembled directly on a paper platform, made conductive with carbon ink and suitable for an electrochemical transduction. The biomimetic material was produced by electropolymerization of phenol after optimizing several experimental parameters, such a scan-rate, number of cycles, range of potential applied, monomer and template concentrations. Under optimal conditions, the label-free sensor was able to respond to 3-NT from 500 nM to 1 mM, yielding a limit of detection of 22.3 nM. Finally, the applicability of the (bio)sensor was tested by performing calibration assays in human urine samples and a good performance was obtained in terms of sensitivity, selectivity and reproducibility. Overall, the attributes of the herein described sensing approach can be compared to a very limited number of other electrochemical devices, that are still using a conventional three electrode system, making this paper-sustained device the first electrochemical (bio)sensor with potential to become a portable and low-cost diagnostic tool for 3-NT. In general, the incorporation of molecular imprinting technology coupled to electrochemical transduction enabled the fabrication of suitable smart sensors for wide screening approaches.
引用
收藏
页数:9
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