4.6 Article

Colloidal Au sphere and nanoflower-based immunochromatographic strips for sensitive detection of zearalenone in cereals

Journal

ANALYTICAL METHODS
Volume 14, Issue 39, Pages 3831-3839

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ay01365g

Keywords

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Funding

  1. National Natural Science Foundation of China [61301037]
  2. Program for Science and Technology Innovation Talents in Universities of Henan Province [20HASTIT002]
  3. Natural Science Foundation of Henan Province of China [212300410338]
  4. Innovative Funds Plan of the Henan University of Technology [2021ZKCJ13]
  5. Open Fund from the Research Platform of the Grain Information Processing Center in the Henan University of Technology [KFJJ-2021-106]
  6. Master's Degree Thesis Cultivation Project of the Henan University of Technology

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In this study, colloidal Au spheres and Au nanoflowers were used as signal labels to detect ZEN in cereals. The sensitivity of the immunochromatographic strip was optimized by adjusting the volume of antigen, antibody, and probe quantities. The use of Au nanoflowers as signal labels showed higher sensitivity compared to traditional colloidal Au spheres, with a low limit of detection of 0.08 ng mL(-1). The Au nanoflowers immunochromatographic strip demonstrated high specificity and sensitivity for ZEN detection.
Zearalenone (ZEN), also known as an F-2 toxin, is a secondary metabolite in the toxic Fusarium species with estrogen properties. ZEN and its derivatives can cause developmental and reproductive disorders in humans and other mammals. In this study, colloidal Au spheres (AuSPs) and Au nanoflowers (AuNFs) were used as signal labels to detect ZEN in cereals, and the critical factors affecting the sensitivity of the immunochromatographic strip (ICS), namely the volume of antigen, antibody, and probe quantities were optimized and compared in detail. Since the large specific surface area of AuNFs reduces the steric hindrance of proteins, it is more conducive to improving the fixation rate of antibodies and proteins. Compared with the traditional colloidal AuSP immunochromatographic strip (AuSP-ICS), the volume of the antibody used in the AuNF immunochromatographic strip (AuNF-ICS) was 0.6 times that in the AuSPs-ICS. At the same antigen volume, a lower amount of probe can achieve the desired visual detection effect and higher sensitivity. For the AuNF-ICS, the limit of detection (LOD) was as low as 0.08 ng mL(-1). ZEN could be detected quickly and accurately from 0.08-10.2 ng mL(-1). And the AuNF-ICS had a high degree of specificity and sensitivity to ZEN. In summary, the AuNF-ICS serves as a valuable tool in large-scale on-site detection of ZEN.

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