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Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875790/ https://www.ncbi.nlm.nih.gov/pubmed/35213967 http://dx.doi.org/10.3390/pharmaceutics14020233 |
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author | Han, Ocean Bromma, Kyle Palmerley, Nicholas Bido, Ariadne T. Monica, Mesa Alhussan, Abdulaziz Howard, Perry L. Brolo, Alexandre G. Beckham, Wayne Alexander, Abraham S. Chithrani, Devika B. |
author_facet | Han, Ocean Bromma, Kyle Palmerley, Nicholas Bido, Ariadne T. Monica, Mesa Alhussan, Abdulaziz Howard, Perry L. Brolo, Alexandre G. Beckham, Wayne Alexander, Abraham S. Chithrani, Devika B. |
author_sort | Han, Ocean |
collection | PubMed |
description | One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offer a two-fold promise as a delivery vehicle for BLM and as a radiosensitizing agent. In this study, GNPs were functionalized and complexed with BLM using a gold-thiol bond (denoted GNP-BLM). Our results show that there was a 40% and 10% decrease in cell growth with GNP-BLM vs. free BLM for the MIA PaCa-2 and PC-3 cell lines, respectively. Testing the GNP-BLM platform with RT showed an 84% and 13% reduction in cell growth in MIA PaCa-2 cells treated with GNP-BLM and GNPs, respectively. Similar results were seen with PC-3 cells. The efficacy of this approach was verified by mapping DNA double-strand breaks (DSBs) as well. Therefore, this proposed incorporation of nanomedicine with RT is promising in achieving a significantly higher therapeutic ratio which is necessary to make a paradigm change to the current clinical approach. |
format | Online Article Text |
id | pubmed-8875790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88757902022-02-26 Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin Han, Ocean Bromma, Kyle Palmerley, Nicholas Bido, Ariadne T. Monica, Mesa Alhussan, Abdulaziz Howard, Perry L. Brolo, Alexandre G. Beckham, Wayne Alexander, Abraham S. Chithrani, Devika B. Pharmaceutics Article One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offer a two-fold promise as a delivery vehicle for BLM and as a radiosensitizing agent. In this study, GNPs were functionalized and complexed with BLM using a gold-thiol bond (denoted GNP-BLM). Our results show that there was a 40% and 10% decrease in cell growth with GNP-BLM vs. free BLM for the MIA PaCa-2 and PC-3 cell lines, respectively. Testing the GNP-BLM platform with RT showed an 84% and 13% reduction in cell growth in MIA PaCa-2 cells treated with GNP-BLM and GNPs, respectively. Similar results were seen with PC-3 cells. The efficacy of this approach was verified by mapping DNA double-strand breaks (DSBs) as well. Therefore, this proposed incorporation of nanomedicine with RT is promising in achieving a significantly higher therapeutic ratio which is necessary to make a paradigm change to the current clinical approach. MDPI 2022-01-20 /pmc/articles/PMC8875790/ /pubmed/35213967 http://dx.doi.org/10.3390/pharmaceutics14020233 Text en © 2022 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 Han, Ocean Bromma, Kyle Palmerley, Nicholas Bido, Ariadne T. Monica, Mesa Alhussan, Abdulaziz Howard, Perry L. Brolo, Alexandre G. Beckham, Wayne Alexander, Abraham S. Chithrani, Devika B. Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title | Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title_full | Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title_fullStr | Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title_full_unstemmed | Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title_short | Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin |
title_sort | nanotechnology driven cancer chemoradiation: exploiting the full potential of radiotherapy with a unique combination of gold nanoparticles and bleomycin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875790/ https://www.ncbi.nlm.nih.gov/pubmed/35213967 http://dx.doi.org/10.3390/pharmaceutics14020233 |
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