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In Situ Shape Control of Thermoplasmonic Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell Detachment
[Image: see text] Gold nanostars (AuNSTs) are biocompatible, have large surface areas, and are characterized by high near-infrared extinction, making them ideal for integration with technologies targeting biological applications. We have developed a robust and simple microfluidic method for the dire...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706095/ https://www.ncbi.nlm.nih.gov/pubmed/33274287 http://dx.doi.org/10.1021/acscentsci.0c01097 |
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author | Vinnacombe-Willson, Gail A. Chiang, Naihao Scarabelli, Leonardo Hu, Yuan Heidenreich, Liv K. Li, Xi Gong, Yao Inouye, Derek T. Fisher, Timothy S. Weiss, Paul S. Jonas, Steven J. |
author_facet | Vinnacombe-Willson, Gail A. Chiang, Naihao Scarabelli, Leonardo Hu, Yuan Heidenreich, Liv K. Li, Xi Gong, Yao Inouye, Derek T. Fisher, Timothy S. Weiss, Paul S. Jonas, Steven J. |
author_sort | Vinnacombe-Willson, Gail A. |
collection | PubMed |
description | [Image: see text] Gold nanostars (AuNSTs) are biocompatible, have large surface areas, and are characterized by high near-infrared extinction, making them ideal for integration with technologies targeting biological applications. We have developed a robust and simple microfluidic method for the direct growth of anisotropic AuNSTs on oxide substrates including indium tin oxide and glass. The synthesis was optimized to yield AuNSTs with high anisotropy, branching, uniformity, and density in batch and microfluidic systems for optimal light-to-heat conversion upon laser irradiation. Surface-enhanced Raman scattering spectra and mesoscale temperature measurements were combined with spatially correlated scanning electron microscopy to monitor nanostar and ligand stability and microbubble formation at different laser fluences. The capability of the platform for generating controlled localized heating was used to explore hyperthermia-assisted detachment of adherent glioblastoma cells (U87-GFP) grafted to the capillary walls. Both flow and laser fluence can be tuned to induce different biological responses, such as ablation, cell deformation, release of intracellular components, and the removal of intact cells. Ultimately, this platform has potential applications in biological and chemical sensing, hyperthermia-mediated drug delivery, and microfluidic soft-release of grafted cells with single-cell specificity. |
format | Online Article Text |
id | pubmed-7706095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77060952020-12-02 In Situ Shape Control of Thermoplasmonic Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell Detachment Vinnacombe-Willson, Gail A. Chiang, Naihao Scarabelli, Leonardo Hu, Yuan Heidenreich, Liv K. Li, Xi Gong, Yao Inouye, Derek T. Fisher, Timothy S. Weiss, Paul S. Jonas, Steven J. ACS Cent Sci [Image: see text] Gold nanostars (AuNSTs) are biocompatible, have large surface areas, and are characterized by high near-infrared extinction, making them ideal for integration with technologies targeting biological applications. We have developed a robust and simple microfluidic method for the direct growth of anisotropic AuNSTs on oxide substrates including indium tin oxide and glass. The synthesis was optimized to yield AuNSTs with high anisotropy, branching, uniformity, and density in batch and microfluidic systems for optimal light-to-heat conversion upon laser irradiation. Surface-enhanced Raman scattering spectra and mesoscale temperature measurements were combined with spatially correlated scanning electron microscopy to monitor nanostar and ligand stability and microbubble formation at different laser fluences. The capability of the platform for generating controlled localized heating was used to explore hyperthermia-assisted detachment of adherent glioblastoma cells (U87-GFP) grafted to the capillary walls. Both flow and laser fluence can be tuned to induce different biological responses, such as ablation, cell deformation, release of intracellular components, and the removal of intact cells. Ultimately, this platform has potential applications in biological and chemical sensing, hyperthermia-mediated drug delivery, and microfluidic soft-release of grafted cells with single-cell specificity. American Chemical Society 2020-10-23 2020-11-25 /pmc/articles/PMC7706095/ /pubmed/33274287 http://dx.doi.org/10.1021/acscentsci.0c01097 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Vinnacombe-Willson, Gail A. Chiang, Naihao Scarabelli, Leonardo Hu, Yuan Heidenreich, Liv K. Li, Xi Gong, Yao Inouye, Derek T. Fisher, Timothy S. Weiss, Paul S. Jonas, Steven J. In Situ Shape Control of Thermoplasmonic Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell Detachment |
title | In Situ Shape Control of Thermoplasmonic
Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell
Detachment |
title_full | In Situ Shape Control of Thermoplasmonic
Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell
Detachment |
title_fullStr | In Situ Shape Control of Thermoplasmonic
Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell
Detachment |
title_full_unstemmed | In Situ Shape Control of Thermoplasmonic
Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell
Detachment |
title_short | In Situ Shape Control of Thermoplasmonic
Gold Nanostars on Oxide Substrates for Hyperthermia-Mediated Cell
Detachment |
title_sort | in situ shape control of thermoplasmonic
gold nanostars on oxide substrates for hyperthermia-mediated cell
detachment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706095/ https://www.ncbi.nlm.nih.gov/pubmed/33274287 http://dx.doi.org/10.1021/acscentsci.0c01097 |
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