4.7 Article

Universal fluorescence nanoprobes to enhance the sensitivity of immunochromatographic assay for detection of 17β-estradiol in milk

Journal

FOOD CHEMISTRY
Volume 370, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2021.131027

Keywords

17 beta-Estradiol; Immunoassay; Rapid detection; Estrogen pollution; ICA

Funding

  1. National Research Program of China [2018YFC1602802]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20-1864]
  3. National First-class Discipline Program of Food Science and Technology [JUFSTR20180303]
  4. Collaborative Innovation Center for Food Safety and Quality Control

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This study focused on the detection of estrogens in the environment and food using on-site immunochromatographic assay method. They developed universal probes based on quantum dot nanobeads and recombinant protein A, achieving enhanced sensitivity for the detection system. The proposed ICA system showed promising results for the rapid and sensitive detection of small-molecule pollutants in environmental and food samples.
The pollution caused by estrogens in the environment and food has received increasing attention. It is still challenging for on-site immunochromatographic assay (ICA) detection of estrogens. The performance of the prepared probes plays a decisive role in the sensitivity and stability of the ICA system. The published probes usually directly couple the detection antibody to the label, ignoring the influence of the label on the activity of the antibody. In this study, 17 beta-estradiol (E-2) was used as a model analyte for the ICA system. Two universal probes were constructed based on quantum dot nanobeads (QBs), recombinant protein A (SPA, from Staphylococcus aureus), and rabbit anti-mouse immunoglobulin G antibody (anti-IgG). The probes were prepared by coupling QBs with SPA, releasing anti-E-2 monoclonal antibody (mAb), and maintaining its activity. The prepared universal probes can orient recognize the Fc region of mAb and fully expose its Fab region, improving the detection sensitivity of the ICA system. The free anti-E-2 mAb and the universal probe (QBs@SPA or QBs@SPA@anti-IgG) were used as the detection antibodies and signal donors, respectively. The results show that the proposed ICA based on QBs@SPA and QBs@SPA@anti-IgG probes could detect E-2 with IC50 of 8.83 and 0.93 ng/mL, respectively, within 15 min under optimal conditions. The recovery results of ICA based on QBs@SPA and QBs@SPA@anti-IgG probes showed good agreement with the findings of the high-performance liquid chromatography (HPLC) analysis for spiked samples. The developed ICA system based on universal probes was superior in terms of sensitivity, rapidity, and applicability, and held great promise for its implementation in detecting environmental and food small-molecule pollutants.

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