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Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy

Label-free live cell imaging was performed using a custom-built high-speed confocal Raman microscopy system. For various cell types, cell-intrinsic Raman bands were monitored. The high-resolution temporal Raman images clearly delineated the intracellular distribution of biologically important molecu...

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Detalles Bibliográficos
Autores principales: Kang, Jeon Woong, Nguyen, Freddy T., Lue, Niyom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269874/
https://www.ncbi.nlm.nih.gov/pubmed/34279303
http://dx.doi.org/10.3390/ma14133732
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author Kang, Jeon Woong
Nguyen, Freddy T.
Lue, Niyom
author_facet Kang, Jeon Woong
Nguyen, Freddy T.
Lue, Niyom
author_sort Kang, Jeon Woong
collection PubMed
description Label-free live cell imaging was performed using a custom-built high-speed confocal Raman microscopy system. For various cell types, cell-intrinsic Raman bands were monitored. The high-resolution temporal Raman images clearly delineated the intracellular distribution of biologically important molecules such as protein, lipid, and DNA. Furthermore, optical phase delay measured using quantitative phase microscopy shows similarity with the image reconstructed from the protein Raman peak. This reported work demonstrates that Raman imaging is a powerful label-free technique for studying various biomedical problems in vitro with minimal sample preparation and external perturbation to the cellular system.
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spelling pubmed-82698742021-07-10 Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy Kang, Jeon Woong Nguyen, Freddy T. Lue, Niyom Materials (Basel) Article Label-free live cell imaging was performed using a custom-built high-speed confocal Raman microscopy system. For various cell types, cell-intrinsic Raman bands were monitored. The high-resolution temporal Raman images clearly delineated the intracellular distribution of biologically important molecules such as protein, lipid, and DNA. Furthermore, optical phase delay measured using quantitative phase microscopy shows similarity with the image reconstructed from the protein Raman peak. This reported work demonstrates that Raman imaging is a powerful label-free technique for studying various biomedical problems in vitro with minimal sample preparation and external perturbation to the cellular system. MDPI 2021-07-03 /pmc/articles/PMC8269874/ /pubmed/34279303 http://dx.doi.org/10.3390/ma14133732 Text en © 2021 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 Article
Kang, Jeon Woong
Nguyen, Freddy T.
Lue, Niyom
Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title_full Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title_fullStr Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title_full_unstemmed Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title_short Temporal Imaging of Live Cells by High-Speed Confocal Raman Microscopy
title_sort temporal imaging of live cells by high-speed confocal raman microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269874/
https://www.ncbi.nlm.nih.gov/pubmed/34279303
http://dx.doi.org/10.3390/ma14133732
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