Back to Search Start Over

Probeless and label-free impedimetric biosensing of D-dimer using gold nanoparticles conjugated with dihexadecylphosphate on screen-printed carbon electrodes

Authors :
Márcio Sousa Góes
Nikola Tasić
Thiago R.L.C. Paixão
Luís Moreira Gonçalves
Letícia Cavalcante
Elenice Deffune
Universidade de São Paulo (USP)
Universidade Estadual Paulista (UNESP)
Universidade Federal da Integração Latino-Americana (UNILA)
Source :
Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP, Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual), Universidade de São Paulo (USP), instacron:USP
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Made available in DSpace on 2022-05-01T09:47:13Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-11-20 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Fundação Araucária D-dimer (DD) is a clinical biomarker of emerging significance. Its fast analysis and quantification, preferably by the bedside, helps a medical doctor make crucial decisions. Electrochemical biosensors are point-of-care technologies that can address such issues. Herein, it is developed a probeless and label-free impedimetric DD biosensor. Gold nanoparticles (AuNPs) are dispersed along with dihexadecylphosphate (DHP) on the surface of screen-printed carbon electrodes (SPCEs) to attach anti-DD monoclonal antibody as sensing recognition element, and the measurements are performed using electrochemical impedance spectroscopy (EIS). Two different analytical models are used to interpret raw impedance spectra. The first model is based on the capacitive response within the DHP monolayer and its electrochemical occupancy described by the complex capacitance value at the frequency of 200 mHz, noted as M1. The second model is based on the charge transfer resistance changes (Rct) occurring upon the mAb-DD binding event, fitted by two different Randles types of the equivalent circuits (noted as M2a and M2b). The models are compared, and with the obtained high linearity in the clinically relevant range (up to 500 ng mL−1) and low levels of detection (as low as 8.92 ng mL−1), a potential POC sensor is demonstrated. Additionally, the proposed sensor is applied in real whole blood samples showing good recovery values with certain discrepancies from the standard laboratory assay result, making a cheap and straightforward way for semi-quantitative bedside clinical evaluation. Departamento de Química Fundamental Instituto de Química Universidade de São Paulo (USP) São Paulo State Univ UNESP Botucatu Medical School Blood Transfusion Center Cell Engineering Lab Centro Interdisciplinar de Ciências da Natureza Instituto Latino-Americano de Ciências da Vida e da Natureza Universidade Federal da Integração Latino-Americana (UNILA) São Paulo State Univ UNESP Botucatu Medical School Blood Transfusion Center Cell Engineering Lab CAPES: 001 FAPESP: 2018/08782-1 FAPESP: 2018/13922-7 FAPESP: 2018/14425-7 Fundação Araucária: FA: 09/2016/PRPPG-42/2016 FAPESP: FAPESP: 2017/10522-5

Details

ISSN :
00134686
Volume :
397
Database :
OpenAIRE
Journal :
Electrochimica Acta
Accession number :
edsair.doi.dedup.....f1dd3dbeac701ef901d0cd23cc40d2c1