分析与检测

基于普鲁士蓝纳米粒子的免疫层析法检测小麦中的呕吐毒素

  • 章铜 ,
  • 沈央红 ,
  • 张雯 ,
  • 朱军莉 ,
  • 陆海霞 ,
  • 刘兴泉
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  • 1(浙江工商大学 食品与生物工程学院,浙江省食品安全重点实验室,浙江 杭州,310018)
    2(浙江农林大学 食品与健康学院,浙江 杭州,311300)
第一作者:硕士研究生(朱军莉教授和陆海霞副教授为共同通信作者,E-mail:junlizhu0305@163.com;luhaixia77@zjgsu.edu.cn)

收稿日期: 2023-03-20

  修回日期: 2023-05-19

  网络出版日期: 2024-03-15

基金资助

省“三农九方”科技计划协作项目(2022SNJF011);省尖兵领雁研发攻关计划项目(2023C02026)

Based on Prussian blue nanoparticles for immunochromatographic detection of deoxynivalenol in wheat

  • ZHANG Tong ,
  • SHEN Yanghong ,
  • ZHANG Wen ,
  • ZHU Junli ,
  • LU Haixia ,
  • LIU Xingquan
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  • 1(School of Food Science & Biotechnology, Zhejiang Gongshang University, Zhejiang Key Laboratory of Food Safety, Hangzhou 310018, China)
    2(School of Food and Health, Zhejiang A&F University, Hangzhou 311300, China)

Received date: 2023-03-20

  Revised date: 2023-05-19

  Online published: 2024-03-15

摘要

该研究采用普鲁士蓝纳米粒子(Prussian blue nanoparticles,PBNPs)作为信号标签,通过制备PBNPs和聚多巴胺包裹普鲁士蓝纳米粒子(polydopamine coated Prussian blue nanoparticles,PB@PDA),优化测试参数、测试试纸条灵敏度和特异性等,研究PBNPs和PB@PDA对呕吐毒素(deoxynivalenol,DON)的检测性能。结果表明,在最优实验条件下,所构建的基于PBNPs和PB@PDA的免疫层析试纸条对DON标准溶液视觉检出限分别为1.0 ng/mL和 0.2 ng/mL,在0.1~0.5 ng/mL保持良好的线性关系,PB@PDA比PBNPs-LFIA检测灵敏度提高5倍,2种试纸条均显示良好的特异性。将PBNPs和PB@PDA两种试纸条应用于小麦样品检测,显示试纸条能排除小麦基质干扰,其检测限分别为20 ng/g和5 ng/g,且PB@PDA检测灵敏度高于商品化胶体金试纸条(10 ng/g)。可见,PB@PDA试纸条表现高灵敏性和抗干扰性,可满足呕吐毒素国家安全标准的限量检测要求,为现场快速筛查小麦中呕吐毒素污染提供一种新方法。

本文引用格式

章铜 , 沈央红 , 张雯 , 朱军莉 , 陆海霞 , 刘兴泉 . 基于普鲁士蓝纳米粒子的免疫层析法检测小麦中的呕吐毒素[J]. 食品与发酵工业, 2024 , 50(4) : 286 -293 . DOI: 10.13995/j.cnki.11-1802/ts.035542

Abstract

Mycotoxin contamination such as deoxynivalenol (DON) in cereals and feed is still serious, and rapid detection of DON is a prerequisite for effective control. In this study, Prussian blue nanoparticles (PBNPs) were used as signal tags in the immunochromatographic detection of DON. PBNPs and polydopamine-coated PBNPs (PB@PDA) were prepared for the sensitive detection of DON in wheat. The test parameters, sensitivity and specificity of test strips were optimized. The results showed that under the optimal experimental conditions, the visual detection limits of DON standard solution based on PBNPs and PB@PDA were 1.0 ng/mL and 0.2 ng/mL, respectively, and maintained a good linear relationship between 0.1 and 0.5 ng/mL. Compared with PBNPs, the sensitivity of PB@PDA increased by 5 times, and both test strips showed good specificity. PBNPs and PB@PDA strips were applied in the detection of DON in wheat samples, with detection limits of 1 ng/g and 0.3 ng/g, respectively. The sensitivity of PB@PDA was also higher than that of commercial colloidal gold strips. Thus, these results indicated that PB@PDA strips with high sensitivity and strong tolerance could reach the limit requirements of national safety standards, which would provide a new method for rapid screening of DON on site.

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