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Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
Stimulated Raman scattering (SRS) microscopy in tandem with bioorthogonal Raman labelling strategies is set to revolutionise the direct visualisation of intracellular drug uptake. Rational evaluation of a series of Raman-active labels has allowed the identification of highly active labels which have...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103005/ https://www.ncbi.nlm.nih.gov/pubmed/30155229 http://dx.doi.org/10.1039/c7sc01837a |
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author | Tipping, William J. Lee, Martin Serrels, Alan Brunton, Valerie G. Hulme, Alison N. |
author_facet | Tipping, William J. Lee, Martin Serrels, Alan Brunton, Valerie G. Hulme, Alison N. |
author_sort | Tipping, William J. |
collection | PubMed |
description | Stimulated Raman scattering (SRS) microscopy in tandem with bioorthogonal Raman labelling strategies is set to revolutionise the direct visualisation of intracellular drug uptake. Rational evaluation of a series of Raman-active labels has allowed the identification of highly active labels which have minimal perturbation on the biological efficacy of the parent drug. Drug uptake has been correlated with markers of cellular composition and cell cycle status, and mapped across intracellular structures using dual-colour and multi-modal imaging. The minimal phototoxicity and low photobleaching associated with SRS microscopy has enabled real-time imaging in live cells. These studies demonstrate the potential for SRS microscopy in the drug development process. |
format | Online Article Text |
id | pubmed-6103005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-61030052018-08-28 Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy Tipping, William J. Lee, Martin Serrels, Alan Brunton, Valerie G. Hulme, Alison N. Chem Sci Chemistry Stimulated Raman scattering (SRS) microscopy in tandem with bioorthogonal Raman labelling strategies is set to revolutionise the direct visualisation of intracellular drug uptake. Rational evaluation of a series of Raman-active labels has allowed the identification of highly active labels which have minimal perturbation on the biological efficacy of the parent drug. Drug uptake has been correlated with markers of cellular composition and cell cycle status, and mapped across intracellular structures using dual-colour and multi-modal imaging. The minimal phototoxicity and low photobleaching associated with SRS microscopy has enabled real-time imaging in live cells. These studies demonstrate the potential for SRS microscopy in the drug development process. Royal Society of Chemistry 2017-08-01 2017-05-24 /pmc/articles/PMC6103005/ /pubmed/30155229 http://dx.doi.org/10.1039/c7sc01837a Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Tipping, William J. Lee, Martin Serrels, Alan Brunton, Valerie G. Hulme, Alison N. Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy |
title | Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
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title_full | Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
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title_fullStr | Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
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title_full_unstemmed | Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
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title_short | Imaging drug uptake by bioorthogonal stimulated Raman scattering microscopy
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title_sort | imaging drug uptake by bioorthogonal stimulated raman scattering microscopy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103005/ https://www.ncbi.nlm.nih.gov/pubmed/30155229 http://dx.doi.org/10.1039/c7sc01837a |
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