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一种侧向流条带的开发,具有正向读出功能,用于现场检测黄曲霉毒素 B。

Development of a Lateral Flow Strip with a Positive Readout for the On-Site Detection of Aflatoxin B.

机构信息

Department of Preventive Medicine, Changzhi Medical College, Changzhi 046000, China.

Department of Chemistry, Changzhi University, Changzhi 046011, China.

出版信息

Molecules. 2022 Aug 3;27(15):4949. doi: 10.3390/molecules27154949.

Abstract

Aflatoxin B is one of the contamination indicators for food safety monitoring. The rapid and effective assessment and determination of AFB 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 requires a competitive format that produces readings inversely proportional to the AFB 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. This Apt-strip relies on the competition between AFB and fluorescein-labeled complementary DNA strands (FAM-cDNA) for affinity binding to limited aptamers against AFB (AFB-Apt). In the absence of AFB, AFB-Apt hybridizes with FAM-cDNA. No signal at the T-line of the Apt-strip was observed. In contrast, AFB-Apt binds to AFB in the sample, and then a part of the FAM-cDNA is hybridized with the free AFB-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 with a detection limit (DL) of 0.1 ng/mL, positive readout, and increased sensitivity.

摘要

黄曲霉毒素 B 是食品安全监测的污染指标之一。快速有效地评估和测定食品中的 AFB 对于饮食安全至关重要。侧向流动分析在其简单性和快速性方面表现出优势,并提供直观的读数,而现有的 AFB 侧向流动分析需要竞争格式,其读数与 AFB 浓度成反比,这有违直觉,可能导致对结果的潜在误解。在此,我们开发了一种基于正读码的适体侧向流动条(Apt-strip)用于检测 AFB。该 Apt-strip 依赖于 AFB 与荧光素标记的互补 DNA 链(FAM-cDNA)之间的竞争,以有限的适体(AFB-Apt)对 AFB 进行亲和结合。在没有 AFB 的情况下,AFB-Apt 与 FAM-cDNA 杂交。在 Apt-strip 的 T 线上未观察到信号。相反,AFB-Apt 在样品中与 AFB 结合,然后一部分 FAM-cDNA 与游离的 AFB-Apt 杂交,此时未反应的其他 FAM-cDNA 被 T 线上的 A35-Apt 捕获。观察到信号。该方法实现了 AFB 的快速检测,检测限(DL)为 0.1ng/mL,具有正读码和更高的灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca3/9370625/57ea5b029c9a/molecules-27-04949-sch001.jpg

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