4.8 Article

A homogeneous immunosensor for AFB1 detection based on FRET between different-sized quantum dots

Journal

BIOSENSORS & BIOELECTRONICS
Volume 56, Issue -, Pages 144-150

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2014.01.007

Keywords

Fluorescence resonance energy transfer; Quantum dots; Aflatoxin B-1; Quantitative immunoassay

Funding

  1. National Basic Research Program of China [2013CB127804]
  2. Twelfth Five-Year Plan for National Science and Technology Support Program [2013BAD19B02, 2012BAK17B02]
  3. Jiangxi Province Main Science and Technology Leader Project [2013BCB22007]
  4. Research Program of the State Key Laboratory of Food Science and Technology, Nanchang University [SKLF-ZZB-201306]

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Mycotoxins are fatal threats in food safety due to their strong carcinogenesis and toxicity, thus requiring highly sensitive detections. Herein, different-sized quantum dots (QDs) were used to construct a Forster resonance energy transfer (FRET) based immunosensor for sensitive detection of aflatoxin B-1 (AFB(1)) in rice grains. To avoid irregular aggregation between two kinds of QDs, monovalent monoclonal antibody (mAb)-labeled red QDs (similar to 0.84 anti-AFB(1) mAbs per QD) and multivalent hapten-labeled green QDs (similar to 6.8 AFB(1) per QD) were designed as acceptor and donor, respectively. The anti-AFB(1) mAbs and AFB(1) interactions promoted one or more acceptors bound with a multivalent AFB(1)-labeled donor, resulting in energy transfer from the green QDs to the red QDs. Various parameters that influence the immunoassay including reactant ratio of donor to acceptor, buffer pH value, buffer ionic strength and immunoreaction time were systematically investigated and optimized. With optimal conditions, the obtained energy transfer efficiency is proportional to the logarithm of AFB(1) concentration in a range over 0.19-16 pM (0.06-5 ng/mL), while offering a limit of detection of 0.13 pM (0.04 ng/mL) in rice extracts. The recovery rates of the intra-assay for spiked samples at AFB(1) concentrations of 0.1, 1.0, and 5.0 ng/mL were 83.27% +/- 3.27%, 97.36% +/- 4.55% and 83.04% +/- 4.94%, respectively, and those for the inter-assay were 81.28% +/- 6.11%, 95.97% +/- 7.07%, and 82.78% +/- 5.99%, respectively. Statistical analysis using t-test had no significant difference between the proposed FRET-based immunoassay and the commercial enzyme-linked immunosorbent assay kit. (C) 2014 Elsevier B.V. All rights reserved.

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