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The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform
Surface enhanced Raman spectroscopy (SERS) is a promising sensing technique that can provide unique chemical and structural fingerprint information, but gaining reliable SERS quantitative data with high sensitivity and stability still remains a challenge. Although using a molecule as an internal sta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033995/ https://www.ncbi.nlm.nih.gov/pubmed/35479874 http://dx.doi.org/10.1039/d1ra01957k |
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author | Wang, Xiao-An Shen, Wei Zhou, Binbin Yu, Daoyang Tang, Xianghu Liu, Jinhuai Huang, Xingjiu |
author_facet | Wang, Xiao-An Shen, Wei Zhou, Binbin Yu, Daoyang Tang, Xianghu Liu, Jinhuai Huang, Xingjiu |
author_sort | Wang, Xiao-An |
collection | PubMed |
description | Surface enhanced Raman spectroscopy (SERS) is a promising sensing technique that can provide unique chemical and structural fingerprint information, but gaining reliable SERS quantitative data with high sensitivity and stability still remains a challenge. Although using a molecule as an internal standard (IS) can improve the SERS quantitative capability, the reliability and SERS measuring conditions for signal fluctuations during calibration based on IS are yet to be explored when the embedded IS molecules and target objects are located in different environments. Herein, a 3D hotspot matrix SERS platform based on Au@4-MPy@AgNPs was constructed in water with the assistance of glycerol and the dynamic signal changes from the IS, i.e. 4-Mpy, and target molecules were monitored during the process of evaporation with high sensitivity and stability. In contrast to the traditional water-dispersed drying film system, the variation trends of IS and target molecules were consistent in the glycerol-assisted liquid film protection system. Therefore, it is reasonable to calibrate the signal fluctuation by utilizing the embedded IS based on the construction strategy of a glycerol-assisted 3D hotspot platform. This work demonstrates a rational, reliable and precise SERS quantitative technique for testing analyte concentrations in practical systems and has great application prospects in the field of analytical chemistry. |
format | Online Article Text |
id | pubmed-9033995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90339952022-04-26 The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform Wang, Xiao-An Shen, Wei Zhou, Binbin Yu, Daoyang Tang, Xianghu Liu, Jinhuai Huang, Xingjiu RSC Adv Chemistry Surface enhanced Raman spectroscopy (SERS) is a promising sensing technique that can provide unique chemical and structural fingerprint information, but gaining reliable SERS quantitative data with high sensitivity and stability still remains a challenge. Although using a molecule as an internal standard (IS) can improve the SERS quantitative capability, the reliability and SERS measuring conditions for signal fluctuations during calibration based on IS are yet to be explored when the embedded IS molecules and target objects are located in different environments. Herein, a 3D hotspot matrix SERS platform based on Au@4-MPy@AgNPs was constructed in water with the assistance of glycerol and the dynamic signal changes from the IS, i.e. 4-Mpy, and target molecules were monitored during the process of evaporation with high sensitivity and stability. In contrast to the traditional water-dispersed drying film system, the variation trends of IS and target molecules were consistent in the glycerol-assisted liquid film protection system. Therefore, it is reasonable to calibrate the signal fluctuation by utilizing the embedded IS based on the construction strategy of a glycerol-assisted 3D hotspot platform. This work demonstrates a rational, reliable and precise SERS quantitative technique for testing analyte concentrations in practical systems and has great application prospects in the field of analytical chemistry. The Royal Society of Chemistry 2021-06-07 /pmc/articles/PMC9033995/ /pubmed/35479874 http://dx.doi.org/10.1039/d1ra01957k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wang, Xiao-An Shen, Wei Zhou, Binbin Yu, Daoyang Tang, Xianghu Liu, Jinhuai Huang, Xingjiu The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title | The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title_full | The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title_fullStr | The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title_full_unstemmed | The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title_short | The rationality of using core–shell nanoparticles with embedded internal standards for SERS quantitative analysis based glycerol-assisted 3D hotspots platform |
title_sort | rationality of using core–shell nanoparticles with embedded internal standards for sers quantitative analysis based glycerol-assisted 3d hotspots platform |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033995/ https://www.ncbi.nlm.nih.gov/pubmed/35479874 http://dx.doi.org/10.1039/d1ra01957k |
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