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Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells

This study describes the use of highly versatile, lithographically defined magnetic microdiscs. Gold covered magnetic microdiscs are used in both radiosensitizing cancer cells, acting as intracellular emitters of secondary electrons during radiotherapy, and as well as inducing mechanical damage by e...

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Detalles Bibliográficos
Autores principales: Leulmi Pichot, Selma, Bentouati, Sabrina, Ahmad, Saif S., Sotiropoulos, Marios, Jena, Raj, Cowburn, Russell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092955/
https://www.ncbi.nlm.nih.gov/pubmed/35558340
http://dx.doi.org/10.1039/d0ra00164c
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author Leulmi Pichot, Selma
Bentouati, Sabrina
Ahmad, Saif S.
Sotiropoulos, Marios
Jena, Raj
Cowburn, Russell
author_facet Leulmi Pichot, Selma
Bentouati, Sabrina
Ahmad, Saif S.
Sotiropoulos, Marios
Jena, Raj
Cowburn, Russell
author_sort Leulmi Pichot, Selma
collection PubMed
description This study describes the use of highly versatile, lithographically defined magnetic microdiscs. Gold covered magnetic microdiscs are used in both radiosensitizing cancer cells, acting as intracellular emitters of secondary electrons during radiotherapy, and as well as inducing mechanical damage by exerting a mechanical torque when exposed to a rotating magnetic field. This study reveals that lithographically defined microdiscs with a uniform size of 2 microns in diameter highly increase the DNA damage and reduce the glioblastoma colony formation potential compared to conventional radiation therapy. Furthermore, the addition of mechanical disruption mediated by the magnetic component of the discs increased the efficiency of brain cancer cell killing.
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spelling pubmed-90929552022-05-11 Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells Leulmi Pichot, Selma Bentouati, Sabrina Ahmad, Saif S. Sotiropoulos, Marios Jena, Raj Cowburn, Russell RSC Adv Chemistry This study describes the use of highly versatile, lithographically defined magnetic microdiscs. Gold covered magnetic microdiscs are used in both radiosensitizing cancer cells, acting as intracellular emitters of secondary electrons during radiotherapy, and as well as inducing mechanical damage by exerting a mechanical torque when exposed to a rotating magnetic field. This study reveals that lithographically defined microdiscs with a uniform size of 2 microns in diameter highly increase the DNA damage and reduce the glioblastoma colony formation potential compared to conventional radiation therapy. Furthermore, the addition of mechanical disruption mediated by the magnetic component of the discs increased the efficiency of brain cancer cell killing. The Royal Society of Chemistry 2020-02-25 /pmc/articles/PMC9092955/ /pubmed/35558340 http://dx.doi.org/10.1039/d0ra00164c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Leulmi Pichot, Selma
Bentouati, Sabrina
Ahmad, Saif S.
Sotiropoulos, Marios
Jena, Raj
Cowburn, Russell
Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title_full Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title_fullStr Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title_full_unstemmed Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title_short Versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
title_sort versatile magnetic microdiscs for the radio enhancement and mechanical disruption of glioblastoma cancer cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092955/
https://www.ncbi.nlm.nih.gov/pubmed/35558340
http://dx.doi.org/10.1039/d0ra00164c
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