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Multicolor Photoluminescent Carbon Dots à La Carte for Biomedical Applications
[Image: see text] Dual-emission fluorescence probes that provide high sensitivity are key for biomedical diagnostic applications. Nontoxic carbon dots (CDs) are an emerging alternative to traditional fluorescent probes; however, robust and reproducible synthetic strategies are still needed to access...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540137/ https://www.ncbi.nlm.nih.gov/pubmed/37715711 http://dx.doi.org/10.1021/acsami.3c08200 |
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author | Garcia-Millan, Teodoro Ramos-Soriano, Javier Ghirardello, Mattia Liu, Xia Santi, Cristina Manuela Eloi, Jean-Charles Pridmore, Natalie Harniman, Robert L. Morgan, David J. Hughes, Stephen Davis, Sean A. Oliver, Thomas A. A. Kurian, Kathreena M. Galan, M. Carmen |
author_facet | Garcia-Millan, Teodoro Ramos-Soriano, Javier Ghirardello, Mattia Liu, Xia Santi, Cristina Manuela Eloi, Jean-Charles Pridmore, Natalie Harniman, Robert L. Morgan, David J. Hughes, Stephen Davis, Sean A. Oliver, Thomas A. A. Kurian, Kathreena M. Galan, M. Carmen |
author_sort | Garcia-Millan, Teodoro |
collection | PubMed |
description | [Image: see text] Dual-emission fluorescence probes that provide high sensitivity are key for biomedical diagnostic applications. Nontoxic carbon dots (CDs) are an emerging alternative to traditional fluorescent probes; however, robust and reproducible synthetic strategies are still needed to access materials with controlled emission profiles and improved fluorescence quantum yields (FQYs). Herein, we report a practical and general synthetic strategy to access dual-emission CDs with FQYs as high as 0.67 and green/blue, yellow/blue, or red/blue excitation-dependent emission profiles using common starting materials such as citric acid, cysteine, and co-dopants to bias the synthetic pathway. Structural and physicochemical analysis using nuclear magnetic resonance, absorbance and fluorescence spectroscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy in addition to transmission electron and atomic force microscopy (TEM and AFM) is used to elucidate the material’s composition which is responsible for the unique observed photoluminescence properties. Moreover, the utility of the probes is demonstrated in the clinical setting by the synthesis of green/blue emitting antibody-CD conjugates which are used for the immunohistochemical staining of human brain tissues of glioblastoma patients, showing detection under two different emission channels. |
format | Online Article Text |
id | pubmed-10540137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105401372023-09-30 Multicolor Photoluminescent Carbon Dots à La Carte for Biomedical Applications Garcia-Millan, Teodoro Ramos-Soriano, Javier Ghirardello, Mattia Liu, Xia Santi, Cristina Manuela Eloi, Jean-Charles Pridmore, Natalie Harniman, Robert L. Morgan, David J. Hughes, Stephen Davis, Sean A. Oliver, Thomas A. A. Kurian, Kathreena M. Galan, M. Carmen ACS Appl Mater Interfaces [Image: see text] Dual-emission fluorescence probes that provide high sensitivity are key for biomedical diagnostic applications. Nontoxic carbon dots (CDs) are an emerging alternative to traditional fluorescent probes; however, robust and reproducible synthetic strategies are still needed to access materials with controlled emission profiles and improved fluorescence quantum yields (FQYs). Herein, we report a practical and general synthetic strategy to access dual-emission CDs with FQYs as high as 0.67 and green/blue, yellow/blue, or red/blue excitation-dependent emission profiles using common starting materials such as citric acid, cysteine, and co-dopants to bias the synthetic pathway. Structural and physicochemical analysis using nuclear magnetic resonance, absorbance and fluorescence spectroscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy in addition to transmission electron and atomic force microscopy (TEM and AFM) is used to elucidate the material’s composition which is responsible for the unique observed photoluminescence properties. Moreover, the utility of the probes is demonstrated in the clinical setting by the synthesis of green/blue emitting antibody-CD conjugates which are used for the immunohistochemical staining of human brain tissues of glioblastoma patients, showing detection under two different emission channels. American Chemical Society 2023-09-16 /pmc/articles/PMC10540137/ /pubmed/37715711 http://dx.doi.org/10.1021/acsami.3c08200 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Garcia-Millan, Teodoro Ramos-Soriano, Javier Ghirardello, Mattia Liu, Xia Santi, Cristina Manuela Eloi, Jean-Charles Pridmore, Natalie Harniman, Robert L. Morgan, David J. Hughes, Stephen Davis, Sean A. Oliver, Thomas A. A. Kurian, Kathreena M. Galan, M. Carmen Multicolor Photoluminescent Carbon Dots à La Carte for Biomedical Applications |
title | Multicolor
Photoluminescent Carbon Dots à La
Carte for Biomedical Applications |
title_full | Multicolor
Photoluminescent Carbon Dots à La
Carte for Biomedical Applications |
title_fullStr | Multicolor
Photoluminescent Carbon Dots à La
Carte for Biomedical Applications |
title_full_unstemmed | Multicolor
Photoluminescent Carbon Dots à La
Carte for Biomedical Applications |
title_short | Multicolor
Photoluminescent Carbon Dots à La
Carte for Biomedical Applications |
title_sort | multicolor
photoluminescent carbon dots à la
carte for biomedical applications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540137/ https://www.ncbi.nlm.nih.gov/pubmed/37715711 http://dx.doi.org/10.1021/acsami.3c08200 |
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