A sensitive SERS-based assay technique for accurate detection of foodborne pathogens without interference.

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Xiangru Bai, Wei Luo, Wenyu Zhou, Wei Chen, Xinling Guo, Aiguo Shen, Jiming Hu
{"title":"A sensitive SERS-based assay technique for accurate detection of foodborne pathogens without interference.","authors":"Xiangru Bai, Wei Luo, Wenyu Zhou, Wei Chen, Xinling Guo, Aiguo Shen, Jiming Hu","doi":"10.1039/d4ay01555j","DOIUrl":null,"url":null,"abstract":"<p><p>The accurate and sensitive detection of foodborne pathogens is critical for timely food quality supervision and human health. To address this issue, herein, we developed a simple and novel surface-enhanced Raman scattering (SERS) assay using <i>p</i>-mercaptobenzoic acid (MBN)-modified gold nanoparticles (Au NPs) and magnetic beads for interference-free detection of <i>Escherichia coli</i> (<i>E. coli</i>). This assay technique cleverly reduced silver ions (Ag<sup>+</sup>) on the surface of <i>E. coli</i> (bacteria@Ag NPs), and the functionalized magnetic beads (capture probes) captured and enriched bacteria@Ag NPs, forming the structure of the capture probes-bacteria@Ag NPs. Then, the capture probes-bacteria@Ag NPs were dissolved in the acidic medium, and the Ag NPs on the surface of <i>E. coli</i> was converted to Ag<sup>+</sup> again. Due to the special coordination between Ag<sup>+</sup> and MBN-modified Au NPs (functionalized Au NPs), the SERS intensity of MBN exhibited a positive correlation with the <i>E. coli</i> concentration, and the SERS detection assay of <i>E. coli</i> was established. The signal of the functionalized Au NPs located at 2228 cm<sup>-1</sup> perfectly avoided the spectral overlap with coexisting materials in the Raman fingerprint region, which ensured the accuracy of the technique. The controlled aggregation of the functionalized Au NPs ensured the reproducibility and reliability of the detection system; the emergence of MBs greatly reduced the reaction time and made sure the operation was rapid, simple and portable. The limit of detection (LOD) for <i>E. coli</i> was as low as 10 cfu mL<sup>-1</sup>, and the detection assay was successfully applied for the detection of <i>E. coli</i> in bottled water and milk. As a sensitive and accurate analytical technique for the detection of pathogens, this SERS-based method has great potential to be applied in the field of food safety.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Methods","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4ay01555j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The accurate and sensitive detection of foodborne pathogens is critical for timely food quality supervision and human health. To address this issue, herein, we developed a simple and novel surface-enhanced Raman scattering (SERS) assay using p-mercaptobenzoic acid (MBN)-modified gold nanoparticles (Au NPs) and magnetic beads for interference-free detection of Escherichia coli (E. coli). This assay technique cleverly reduced silver ions (Ag+) on the surface of E. coli (bacteria@Ag NPs), and the functionalized magnetic beads (capture probes) captured and enriched bacteria@Ag NPs, forming the structure of the capture probes-bacteria@Ag NPs. Then, the capture probes-bacteria@Ag NPs were dissolved in the acidic medium, and the Ag NPs on the surface of E. coli was converted to Ag+ again. Due to the special coordination between Ag+ and MBN-modified Au NPs (functionalized Au NPs), the SERS intensity of MBN exhibited a positive correlation with the E. coli concentration, and the SERS detection assay of E. coli was established. The signal of the functionalized Au NPs located at 2228 cm-1 perfectly avoided the spectral overlap with coexisting materials in the Raman fingerprint region, which ensured the accuracy of the technique. The controlled aggregation of the functionalized Au NPs ensured the reproducibility and reliability of the detection system; the emergence of MBs greatly reduced the reaction time and made sure the operation was rapid, simple and portable. The limit of detection (LOD) for E. coli was as low as 10 cfu mL-1, and the detection assay was successfully applied for the detection of E. coli in bottled water and milk. As a sensitive and accurate analytical technique for the detection of pathogens, this SERS-based method has great potential to be applied in the field of food safety.

一种基于 SERS 的灵敏检测技术,可在无干扰的情况下准确检测食源性病原体。
准确灵敏地检测食源性病原体对于及时监督食品质量和人类健康至关重要。为了解决这个问题,我们在本文中利用对巯基苯甲酸(MBN)修饰的金纳米粒子(Au NPs)和磁珠开发了一种简单而新颖的表面增强拉曼散射(SERS)检测方法,用于无干扰检测大肠杆菌(E. coli)。该检测技术巧妙地还原了大肠杆菌(细菌@Ag NPs)表面的银离子(Ag+),功能化磁珠(捕获探针)捕获并富集了细菌@Ag NPs,形成了捕获探针-细菌@Ag NPs的结构。然后,将捕获探针-细菌@Ag NPs溶解在酸性培养基中,大肠杆菌表面的Ag NPs就会重新转化为Ag+。由于 Ag+ 与 MBN 修饰的 Au NPs(功能化 Au NPs)之间的特殊配位,MBN 的 SERS 强度与大肠杆菌浓度呈正相关,从而建立了大肠杆菌的 SERS 检测方法。功能化金 NPs 的信号位于 2228 cm-1 处,完美地避免了与拉曼指纹区域共存物质的光谱重叠,确保了该技术的准确性。功能化 Au NPs 的可控聚集保证了检测系统的重现性和可靠性;MBs 的出现大大缩短了反应时间,确保了操作的快速、简单和便携。大肠杆菌的检测限(LOD)低至 10 cfu mL-1,该检测方法已成功应用于瓶装水和牛奶中大肠杆菌的检测。作为一种灵敏、准确的病原体检测分析技术,这种基于 SERS 的方法在食品安全领域有着巨大的应用潜力。
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
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
×
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