4.7 Article

GO-amplified fluorescence polarization assay for high-sensitivity detection of aflatoxin B1 with low dosage aptamer probe

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 411, Issue 5, Pages 1107-1115

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-018-1540-6

Keywords

Aptamer; Fluorescence polarization; Graphene oxide; Signal amplifier; Aflatoxin B-1

Funding

  1. Science & Technology Support Program of Jiangsu Province [BE2017623]
  2. Jiangsu Agricultural Science and Technology Innovation Fund [CX(18)2025]
  3. National Natural Science Fund of China [31871881]
  4. Fundamental Research Funds for Central Universities [JUSRP51714B]
  5. Distinguished Professor Program of Jiangsu Province
  6. Jiangnan University Postgraduate Overseas Research Project

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Aflatoxin B-1 (AFB(1)) is the most toxic mycotoxin of the aflatoxins (AFs) and shows carcinogenic, teratogenic and mutagenic effects in humans and animals. AFB(1) is widely seen in cereal products such as rice and wheat. This research proposed a low-cost, high-sensitivity fluorescence polarization (FP) assay for detection of AFB(1) using aptamer biosensors based on graphene oxide (GO). The aptamers labelled with fluorescein amidite (FAM) were adsorbed on the surface of GO through - stacking and electrostatic interaction, thus forming aptamer/GO macromolecular complexes. Under these conditions, the local rotation of fluorophores was limited and the system had a high FP value. When there was AFB(1) in the system, aptamers were dissociated from the GO surface and combined with AFB(1) owing to their specificity to form aptamer/AFB(1) complexes. As a result, large changes were observed in the molecular weights of aptamers before, and after, the combination, therefore leading to the apparent changes in FP value. The results showed that when only 10nM of aptamer was used, the changes in FP and the AFB(1) concentration had a favourable linear relationship within 0.05 to 5nM of AFB(1), and the lowest detection limit (LOD) was 0.05nM. In addition, the recoveries of rice sample extract ranged from 89.2% to 112%. The method is simple, highly sensitive, cost-efficient and shows potential application prospects.

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