A new methodology for sub-femtomolar detection of organic molecules through the combination of surface-enhanced Raman spectroscopy and a superhydrophobic fluidic concentrator

IF 3 Q2 CHEMISTRY, ANALYTICAL
Victor Fabre, Franck Carcenac, Adrian Laborde, Jean-Baptiste Doucet, Christophe Vieu, Philippe Louarn, Emmanuelle Trevisiol
{"title":"A new methodology for sub-femtomolar detection of organic molecules through the combination of surface-enhanced Raman spectroscopy and a superhydrophobic fluidic concentrator","authors":"Victor Fabre,&nbsp;Franck Carcenac,&nbsp;Adrian Laborde,&nbsp;Jean-Baptiste Doucet,&nbsp;Christophe Vieu,&nbsp;Philippe Louarn,&nbsp;Emmanuelle Trevisiol","doi":"10.1002/ansa.202400013","DOIUrl":null,"url":null,"abstract":"<p>A specific device that combines (1) surface-enhanced Raman spectroscopy (SERS) and (2) superhydrophobic surfaces is developed to detect traces of analytes diluted at sub-femtomolar concentration in water solutions. The first step of the analysis consists in the evaporation of a drop of the solution on the device, designed to concentrate all the analytes on a central functionalized small area (80 µm diameter). This analytical zone is covered with Ag nanoparticles dedicated to enhance Raman signals. In a second step, this zone is scanned pixel by pixel to accumulate around 2200 Raman spectra. The third step is an algorithmic analysis of the pile of spectra to identify Raman peaks that are specific to the targeted molecules. We detail an original analysis method that allows (1) to select spectra that are significantly different from those obtained when a pure solvent is evaporated (control experiment), (2) to classify the spectra by a criterion of similarity and, finally, (3) to select the SERS spectra of the analytes. This method uses hierarchical correlation clustering techniques, the originality being to classify the different spectra on the basis of their peak positions, with all peaks being normalized at the same intensity and bandwidth. The method leads to a convincing identification of spectra of the targeted molecules (i.e. rhodamine B), down to atto-molar concentrations.</p>","PeriodicalId":93411,"journal":{"name":"Analytical science advances","volume":"6 1","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ansa.202400013","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical science advances","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ansa.202400013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A specific device that combines (1) surface-enhanced Raman spectroscopy (SERS) and (2) superhydrophobic surfaces is developed to detect traces of analytes diluted at sub-femtomolar concentration in water solutions. The first step of the analysis consists in the evaporation of a drop of the solution on the device, designed to concentrate all the analytes on a central functionalized small area (80 µm diameter). This analytical zone is covered with Ag nanoparticles dedicated to enhance Raman signals. In a second step, this zone is scanned pixel by pixel to accumulate around 2200 Raman spectra. The third step is an algorithmic analysis of the pile of spectra to identify Raman peaks that are specific to the targeted molecules. We detail an original analysis method that allows (1) to select spectra that are significantly different from those obtained when a pure solvent is evaporated (control experiment), (2) to classify the spectra by a criterion of similarity and, finally, (3) to select the SERS spectra of the analytes. This method uses hierarchical correlation clustering techniques, the originality being to classify the different spectra on the basis of their peak positions, with all peaks being normalized at the same intensity and bandwidth. The method leads to a convincing identification of spectra of the targeted molecules (i.e. rhodamine B), down to atto-molar concentrations.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.60
自引率
0.00%
发文量
0
×
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