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Development of a Lateral Flow Strip with a Positive Readout for the On-Site Detection of Aflatoxin B(1)
Aflatoxin B(1) is one of the contamination indicators for food safety monitoring. The rapid and effective assessment and determination of AFB(1) in food is of great importance to dietary safety. The lateral flow assay shows advantages in its simplicity, and rapidity, and provides a visual readout, w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9370625/ https://www.ncbi.nlm.nih.gov/pubmed/35956902 http://dx.doi.org/10.3390/molecules27154949 |
Sumario: | Aflatoxin B(1) is one of the contamination indicators for food safety monitoring. The rapid and effective assessment and determination of AFB(1) in food is of great importance to dietary safety. The lateral flow assay shows advantages in its simplicity, and rapidity, and provides a visual readout, while the available lateral flow assay for AFB(1) requires a competitive format that produces readings inversely proportional to the AFB(1) concentration, which is counterintuitive and may lead to a potential misinterpretation of the results. Herein, we developed a positive readout aptamer-based lateral flow strip (Apt-strip) for the detection of AFB(1). This Apt-strip relies on the competition between AFB(1) and fluorescein-labeled complementary DNA strands (FAM-cDNA) for affinity binding to limited aptamers against AFB(1) (AFB(1)-Apt). In the absence of AFB(1), AFB(1)-Apt hybridizes with FAM-cDNA. No signal at the T-line of the Apt-strip was observed. In contrast, AFB(1)-Apt binds to AFB(1) in the sample, and then a part of the FAM-cDNA is hybridized with the free AFB(1)-Apt, at which time the other unreacted FAM-cDNA is captured by A35-Apt on the T-line. The signal was observed. This method achieved fast detection of AFB(1) with a detection limit (DL) of 0.1 ng/mL, positive readout, and increased sensitivity. |
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