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Fluorescent Carbon Dots for Super-Resolution Microscopy

Conventional fluorescence microscopy is limited by the optical diffraction of light, which results in a spatial resolution of about half of the light’s wavelength, approximately to 250–300 nm. The spatial resolution restricts the utilization of microscopes for studying subcellular structures. In ord...

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Detalles Bibliográficos
Autores principales: Sun, Xiangcheng, Mosleh, Nazanin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917526/
https://www.ncbi.nlm.nih.gov/pubmed/36769896
http://dx.doi.org/10.3390/ma16030890
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author Sun, Xiangcheng
Mosleh, Nazanin
author_facet Sun, Xiangcheng
Mosleh, Nazanin
author_sort Sun, Xiangcheng
collection PubMed
description Conventional fluorescence microscopy is limited by the optical diffraction of light, which results in a spatial resolution of about half of the light’s wavelength, approximately to 250–300 nm. The spatial resolution restricts the utilization of microscopes for studying subcellular structures. In order to improve the resolution and to shatter the diffraction limit, two general approaches were developed: a spatially patterned excitation method and a single-molecule localization strategy. The success of super-resolution imaging relies on bright and easily accessible fluorescent probes with special properties. Carbon dots, due to their unique properties, have been used for super-resolution imaging. Considering the importance and fast development of this field, this work focuses on the recent progress and applications of fluorescent carbon dots as probes for super-resolution imaging. The properties of carbon dots for super-resolution microscopy (SRM) are analyzed and discussed. The conclusions and outlook on this topic are also presented.
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spelling pubmed-99175262023-02-11 Fluorescent Carbon Dots for Super-Resolution Microscopy Sun, Xiangcheng Mosleh, Nazanin Materials (Basel) Review Conventional fluorescence microscopy is limited by the optical diffraction of light, which results in a spatial resolution of about half of the light’s wavelength, approximately to 250–300 nm. The spatial resolution restricts the utilization of microscopes for studying subcellular structures. In order to improve the resolution and to shatter the diffraction limit, two general approaches were developed: a spatially patterned excitation method and a single-molecule localization strategy. The success of super-resolution imaging relies on bright and easily accessible fluorescent probes with special properties. Carbon dots, due to their unique properties, have been used for super-resolution imaging. Considering the importance and fast development of this field, this work focuses on the recent progress and applications of fluorescent carbon dots as probes for super-resolution imaging. The properties of carbon dots for super-resolution microscopy (SRM) are analyzed and discussed. The conclusions and outlook on this topic are also presented. MDPI 2023-01-17 /pmc/articles/PMC9917526/ /pubmed/36769896 http://dx.doi.org/10.3390/ma16030890 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sun, Xiangcheng
Mosleh, Nazanin
Fluorescent Carbon Dots for Super-Resolution Microscopy
title Fluorescent Carbon Dots for Super-Resolution Microscopy
title_full Fluorescent Carbon Dots for Super-Resolution Microscopy
title_fullStr Fluorescent Carbon Dots for Super-Resolution Microscopy
title_full_unstemmed Fluorescent Carbon Dots for Super-Resolution Microscopy
title_short Fluorescent Carbon Dots for Super-Resolution Microscopy
title_sort fluorescent carbon dots for super-resolution microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917526/
https://www.ncbi.nlm.nih.gov/pubmed/36769896
http://dx.doi.org/10.3390/ma16030890
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