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金纳米粒子抗体缀合物比色免疫探测真菌毒素。

Mycotoxin Detection through Colorimetric Immunoprobing with Gold Nanoparticle Antibody Conjugates.

机构信息

School of Food Science and Environmental Health, Technological University Dublin, D07 H6K8 Dublin, Ireland.

Nanolab, Physical to Life Sciences Research Hub, Technological University Dublin, D08 CKP1 Dublin, Ireland.

出版信息

Biosensors (Basel). 2024 Oct 10;14(10):491. doi: 10.3390/bios14100491.

DOI:10.3390/bios14100491
PMID:39451705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11506043/
Abstract

Driven by their exceptional optical characteristics, robust chemical stability, and facile bioconjugation, gold nanoparticles (AuNPs) have emerged as a preferred material for detection and biosensing applications in scientific research. This study involves the development of a simple, rapid, and cost-effective colorimetric immuno-sensing probe to detect aflatoxin B1 and zearalenone using AuNP antibody (AuNP-mAb) conjugates. Anti-toxin antibodies were attached to the AuNPs by using the physical adsorption method. The colorimetric immunosensor developed operates on the principle that the optical properties of the AuNP are very sensitive to aggregation, which can be induced by a critical high salt concentration. Although the presence of antibodies on the AuNP surface inhibits the aggregation, these antibodies bind to the toxin with higher affinity, which leads to exposure of the surface of AuNPs and aggregation in a salt environment. The aggregation triggers a noticeable but variable alteration in color from red to purple and blueish gray, as a result of a red shift in the surface plasmon resonance band of the AuNPs. The extent of the shift is dependent on the toxin exposure dose and can be quantified using a calibration curve through UV-Visible-NIR spectroscopy. The limit of detection using this assay was determined to be as low as 0.15 ng/mL for both zearalenone and aflatoxin B1. The specificity of the prepared immunoprobe was analyzed for a particular mycotoxin in the presence of other mycotoxins. The developed immunoprobe was evaluated for real-world applicability using artificially spiked samples. This colorimetric immunoprobe based on localized surface plasmon resonance (LSPR) has a reduced detection limit compared to other immunoassays, a rapid readout, low cost, and facile fabrication.

摘要

受其出色的光学特性、稳健的化学稳定性以及易于生物偶联的特性的驱动,金纳米粒子(AuNPs)已成为科学研究中用于检测和生物传感应用的首选材料。本研究开发了一种简单、快速且具有成本效益的比色免疫传感探针,用于使用 AuNP 抗体(AuNP-mAb)缀合物检测黄曲霉毒素 B1 和玉米赤霉烯酮。通过物理吸附法将抗毒素抗体附着到 AuNPs 上。所开发的比色免疫传感器基于这样的原理运作:AuNP 的光学性质对聚集非常敏感,而高盐浓度会诱导这种聚集。尽管 AuNP 表面上的抗体抑制了聚集,但这些抗体与毒素的结合具有更高的亲和力,这导致 AuNPs 的表面暴露并在盐环境中聚集。这种聚集会导致 AuNPs 的表面等离子体共振带发生明显但可变的红移,从而导致颜色从红色变为紫色和蓝灰色。该转变的程度取决于毒素暴露剂量,可以通过紫外可见近红外光谱(UV-Visible-NIR spectroscopy)使用校准曲线进行定量。使用该测定法的检测限对于玉米赤霉烯酮和黄曲霉毒素 B1 均低至 0.15 ng/mL。在存在其他真菌毒素的情况下,分析了制备的免疫探针对特定真菌毒素的特异性。使用人工添加的样品评估了开发的免疫探针的实际适用性。与其他免疫分析相比,基于局域表面等离子体共振(LSPR)的这种比色免疫探针具有更低的检测限、快速的读数、低成本和易于制造的特点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/d8e9e5dabdb8/biosensors-14-00491-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/00410ad0a747/biosensors-14-00491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/a2c5f93e3069/biosensors-14-00491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/22ce2fd66ada/biosensors-14-00491-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/c92e4686befa/biosensors-14-00491-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/dd15f151fea0/biosensors-14-00491-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/d8e9e5dabdb8/biosensors-14-00491-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/00410ad0a747/biosensors-14-00491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/a2c5f93e3069/biosensors-14-00491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/22ce2fd66ada/biosensors-14-00491-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/c92e4686befa/biosensors-14-00491-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/dd15f151fea0/biosensors-14-00491-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94c/11506043/d8e9e5dabdb8/biosensors-14-00491-g006.jpg

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