4.7 Article

Plasmonic ELISA for naked-eye detection of ochratoxin A based on the tyramine-H2O2 amplification system

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 259, 期 -, 页码 162-169

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2017.12.004

关键词

Immunoassay; Ochratoxin A; Hydrogen peroxide; Gold nanoparticle aggregation; Tyraminea

资金

  1. National Natural Science Foundation of China [31760485]
  2. National Basic Research Program of China [2013CB127804]
  3. Natural Science Foundation of Jiangxi province, China [20161ACB20002]
  4. Nanchang University, China [cx2015107]

向作者/读者索取更多资源

A novel direct competitive plasmonic enzyme-linked immunosorbent assay (dc-pELISA) was applied to detect ochratoxin A (OTA) with naked eyes. In this assay, horseradish peroxidase (HRP) + hydrogen peroxide (H2O2) + tyramine (TYR)-induced gold nanoparticle (AuNP) aggregation was considered as a signal output; AuNP aggregation could be triggered through the phenol polymerization of TYR, which was induced by hydroxyl radicals from HRP-catalyzed H2O2; OTA-labeled catalase (CAT) was used as a competing antigen to consume H2O2. Owing to the combined advantages of ultrahigh CAT catalytic activity for H2O2 and dual-color responses (red and blue) generated through AuNP aggregation, the proposed method was highly sensitive and thus could be employed with naked eyes to detect OTA qualitatively with a cutoff limit of 150 pg/mL. Our method also demonstrated a good dynamic linear range (12.5-150 pg/mL) for quantitative OTA determination with a reliable correlation coefficient of R-2 = 0.992, a half-maximal inhibitory concentration of 84.75 pg/mL, and a detection limit of 17.8 pg/mL. In brief, this newly-designed technique is considerably suitable for high-throughput screening detection or point-of-care diagnostics in resource-constrained regions because of the easy readout of results by naked eyes without the use of advanced detection equipment. (C) 2017 Elsevier B.V. All rights reserved.

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