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基于近红外荧光分子的 5-羟色氨酸侧向流动免疫分析,作为金纳米粒子的替代标记物。

Lateral flow immunoassay for 5-hydroxyflunixin based on near-infrared fluorescence molecule as an alternative label to gold nanoparticles.

机构信息

State Key Laboratory of Animal Nutrition, and Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing, 100193, China.

NBGen Co Ltd., Building 7, Bodaxing Industry Park, BDA, Beijing, 101111, China.

出版信息

Mikrochim Acta. 2020 Jun 3;187(6):368. doi: 10.1007/s00604-020-04338-z.

Abstract

A high-affinity monoclonal antibody (mAb) has been prepared and separately a gold nanoparticle (AuNP)-based and a near-infrared (NIR) fluorescence-based lateral flow immunoassay (LFA) developed for determination of 5-hydroxyflunixin residue in raw milk. The AuNP and IRDye® 800CW were used to label anti-5-hydroxyflunixin mAb to form the AuNP-mAb and NIR dye-mAb conjugates, respectively. Quantitative determination of 5-hydroxyflunixin was achieved by imaging the optical or fluorescence intensity of the AuNP-mAb and NIR dye-mAb captured on the test line. As a result, the detection limits of the AuNP-based LFA and NIR dye-based LFA were 0.82 and 0.073 ng/mL in raw milk, respectively. The considerable improvement on assay sensitivity of the NIR-based LFA can be attributed to the lower background and less antibody consumption per test than that of the AuNP-based LFA. The spiking experiment by the NIR-based LFA yielded 85.7-112.6% recovery with a relative standard deviation below 14%, indicating that it has satisfactory assay accuracy and precision. Furthermore, the analytical results of actual samples by the NIR dye-based LFA were consistent with that by instrumental analysis. Therefore, these results demonstrated that the NIR dye is an ideal alternative label to the conventional AuNP for the development of LFA for veterinary drugs in animal-origin food. Graphical abstract.

摘要

已制备出一种高亲和力的单克隆抗体 (mAb),并分别开发了基于金纳米粒子 (AuNP) 和近红外 (NIR) 荧光的侧向流动免疫分析 (LFA),用于测定生乳中的 5-羟色氨酸残留量。AuNP 和 IRDye® 800CW 分别用于标记抗 5-羟色氨酸 mAb,形成 AuNP-mAb 和 NIR 染料-mAb 缀合物。通过对测试线上捕获的 AuNP-mAb 和 NIR 染料-mAb 的光学或荧光强度进行成像,实现了 5-羟色氨酸的定量测定。结果,基于 AuNP 的 LFA 和基于 NIR 染料的 LFA 的检测限分别为生乳中的 0.82 和 0.073ng/mL。与基于 AuNP 的 LFA 相比,基于 NIR 的 LFA 的检测灵敏度有了显著提高,这归因于其背景更低,每个测试的抗体消耗更少。基于 NIR 的 LFA 的加标实验回收率为 85.7-112.6%,相对标准偏差低于 14%,表明其具有令人满意的分析准确性和精密度。此外,基于 NIR 染料的 LFA 对实际样品的分析结果与仪器分析结果一致。因此,这些结果表明,与传统的 AuNP 相比,NIR 染料是开发动物源性食品中兽药 LFA 的理想替代标记物。

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