A SERS and Fluorescence Dual-Signal Aptasensor for AFB1 Detection Based on DTNB Labeled AuNPs and CdTe Quantum Dots

IF 2.6 3区 农林科学 Q2 FOOD SCIENCE & TECHNOLOGY
Xiaoyuan Ma, Jinxiang Wei, Caiyun Jiang, Zhouping Wang
{"title":"A SERS and Fluorescence Dual-Signal Aptasensor for AFB1 Detection Based on DTNB Labeled AuNPs and CdTe Quantum Dots","authors":"Xiaoyuan Ma,&nbsp;Jinxiang Wei,&nbsp;Caiyun Jiang,&nbsp;Zhouping Wang","doi":"10.1007/s12161-024-02715-5","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, an aptasensor with stable surface-enhanced Raman scattering (SERS) and fluorescence dual-signal output had been developed for the detection of aflatoxin B<sub>1</sub> (AFB<sub>1</sub>). The quantum dots were encapsulated within silica to ensure the stability of fluorescence signal. The gold nanoparticles (AuNPs) were modified with SERS signal molecule DTNB and the complementary sequence (cDNA) of AFB<sub>1</sub> aptamer and then connected on the surface of silica to obtain the signal probes. In the meantime, Fe<sub>3</sub>O<sub>4</sub> was coated with silica which was modified with aptamer to gain capture probes. The two probes could bind specifically based on the base complementary pairing principle. Then, the mixture was separated and gathered by an external magnet. At this time, the maximum SERS signal could be detected in the precipitate, and there was no fluorescence signal in the supernatant. Upon introduction of AFB<sub>1</sub> into the system, the signal probes would be released, resulting in fluorescence recovery in the supernatant while SERS signal weakened in the precipitate. The developed method showed a linear relationship of AFB<sub>1</sub> for the SERS signal in the range of 10<sup>−4</sup>–10<sup>3</sup> ng/mL, with a detection limit of 0.087 pg/mL. The linear range for the fluorescence signal was from 10<sup>−4</sup> to 10<sup>2</sup> ng/mL, with a detection limit of 0.100 pg/mL. The proposed technique was highly sensitive and accurate, which showed promising application prospects in food safety detection.</p></div>","PeriodicalId":561,"journal":{"name":"Food Analytical Methods","volume":"18 2","pages":"293 - 304"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Analytical Methods","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s12161-024-02715-5","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Herein, an aptasensor with stable surface-enhanced Raman scattering (SERS) and fluorescence dual-signal output had been developed for the detection of aflatoxin B1 (AFB1). The quantum dots were encapsulated within silica to ensure the stability of fluorescence signal. The gold nanoparticles (AuNPs) were modified with SERS signal molecule DTNB and the complementary sequence (cDNA) of AFB1 aptamer and then connected on the surface of silica to obtain the signal probes. In the meantime, Fe3O4 was coated with silica which was modified with aptamer to gain capture probes. The two probes could bind specifically based on the base complementary pairing principle. Then, the mixture was separated and gathered by an external magnet. At this time, the maximum SERS signal could be detected in the precipitate, and there was no fluorescence signal in the supernatant. Upon introduction of AFB1 into the system, the signal probes would be released, resulting in fluorescence recovery in the supernatant while SERS signal weakened in the precipitate. The developed method showed a linear relationship of AFB1 for the SERS signal in the range of 10−4–103 ng/mL, with a detection limit of 0.087 pg/mL. The linear range for the fluorescence signal was from 10−4 to 102 ng/mL, with a detection limit of 0.100 pg/mL. The proposed technique was highly sensitive and accurate, which showed promising application prospects in food safety detection.

基于DTNB标记AuNPs和CdTe量子点的AFB1检测的SERS和荧光双信号适体传感器
本文研制了一种具有稳定表面增强拉曼散射(SERS)和荧光双信号输出的适体传感器,用于黄曲霉毒素B1 (AFB1)的检测。量子点被封装在二氧化硅中,以保证荧光信号的稳定性。用SERS信号分子DTNB和AFB1适配体的互补序列cDNA修饰金纳米粒子(AuNPs),然后连接在二氧化硅表面得到信号探针。同时,在Fe3O4表面包覆二氧化硅,二氧化硅经适体修饰后获得捕获探针。基于碱基互补配对原理,两个探针可以特异性结合。然后,混合物被一个外部磁铁分离和聚集。此时沉淀中可检测到最大的SERS信号,上清中无荧光信号。在系统中引入AFB1后,信号探针会被释放,导致上清中的荧光恢复,而沉淀中的SERS信号减弱。在10−4 ~ 103 ng/mL范围内,AFB1对SERS信号呈线性关系,检出限为0.087 pg/mL。荧光信号线性范围为10−4 ~ 102 ng/mL,检出限为0.100 pg/mL。该方法灵敏度高,准确度高,在食品安全检测中具有广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Food Analytical Methods
Food Analytical Methods 农林科学-食品科技
CiteScore
6.00
自引率
3.40%
发文量
244
审稿时长
3.1 months
期刊介绍: Food Analytical Methods publishes original articles, review articles, and notes on novel and/or state-of-the-art analytical methods or issues to be solved, as well as significant improvements or interesting applications to existing methods. These include analytical technology and methodology for food microbial contaminants, food chemistry and toxicology, food quality, food authenticity and food traceability. The journal covers fundamental and specific aspects of the development, optimization, and practical implementation in routine laboratories, and validation of food analytical methods for the monitoring of food safety and quality.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信