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Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study
PURPOSE: The purpose of this study was to determine dose enhancement (DE) and the possible clinical benefits associated with the inclusion of gold nanoparticles (AuNPs) in cancer cells irradiated by either an (192)Ir brachytherapy source or a Xoft(®) Axxent(®) Electronic (eBx™) Brachytherapy. PATIEN...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165788/ https://www.ncbi.nlm.nih.gov/pubmed/30310276 http://dx.doi.org/10.2147/IJN.S174624 |
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author | Shahhoseini, Elham Ramachandran, Prabhakar Patterson, William Roy Geso, Moshi |
author_facet | Shahhoseini, Elham Ramachandran, Prabhakar Patterson, William Roy Geso, Moshi |
author_sort | Shahhoseini, Elham |
collection | PubMed |
description | PURPOSE: The purpose of this study was to determine dose enhancement (DE) and the possible clinical benefits associated with the inclusion of gold nanoparticles (AuNPs) in cancer cells irradiated by either an (192)Ir brachytherapy source or a Xoft(®) Axxent(®) Electronic (eBx™) Brachytherapy. PATIENTS AND METHODS: Brachytherapy DE caused by AuNPs is investigated using two methods, namely (192)Ir and eBx™ Brachytherapy. The second method, which was recently introduced clinically, operates at ~50 kV, which is also the optimal beam energy for DE. In this in vitro study, two cancer cell lines, lung (A549) and prostate (DU145), were used. Cells were incubated with 1 mM (2% w/w) concentration of AuNPs of ~15 nm in size. The control groups were exposed to a range of doses from 0 (control) to 6 Gy, with eBx™ and (192)Ir sources separately. A clonogenic assay was conducted to determine cell survival curves. RESULTS: High dose enhancement factor (DEF) values were achieved in treated groups with low concentration of AuNPs with the 50 kV energy associated with the eBx™. The DE levels in eBx™ for Du145 and A549 cells were found to be 2.90 and 2.06, respectively. The results showed DEFs measured for the same cell lines using (192)Ir brachytherapy to be 1.67 and 1.54 for Du145 and A549 cancer cells, respectively. This clearly indicates that much higher DE values are obtained in the case of eBx™ X-ray brachytherapy compared to (192)Ir gamma brachytherapy. CONCLUSION: The higher DE values obtained with eBx™ compared to (192)Ir brachytherapy can be attributed to the lower average energy of the former and being closer to the optimal energy for DE. This could potentially be utilized by medical practitioners and clinicians to achieve the same tumor control with a significantly lower dose from the eBx™ compared to the (192)Ir brachytherapy treatment, thus bringing huge benefits to the brachytherapy-treated patients. |
format | Online Article Text |
id | pubmed-6165788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61657882018-10-11 Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study Shahhoseini, Elham Ramachandran, Prabhakar Patterson, William Roy Geso, Moshi Int J Nanomedicine Original Research PURPOSE: The purpose of this study was to determine dose enhancement (DE) and the possible clinical benefits associated with the inclusion of gold nanoparticles (AuNPs) in cancer cells irradiated by either an (192)Ir brachytherapy source or a Xoft(®) Axxent(®) Electronic (eBx™) Brachytherapy. PATIENTS AND METHODS: Brachytherapy DE caused by AuNPs is investigated using two methods, namely (192)Ir and eBx™ Brachytherapy. The second method, which was recently introduced clinically, operates at ~50 kV, which is also the optimal beam energy for DE. In this in vitro study, two cancer cell lines, lung (A549) and prostate (DU145), were used. Cells were incubated with 1 mM (2% w/w) concentration of AuNPs of ~15 nm in size. The control groups were exposed to a range of doses from 0 (control) to 6 Gy, with eBx™ and (192)Ir sources separately. A clonogenic assay was conducted to determine cell survival curves. RESULTS: High dose enhancement factor (DEF) values were achieved in treated groups with low concentration of AuNPs with the 50 kV energy associated with the eBx™. The DE levels in eBx™ for Du145 and A549 cells were found to be 2.90 and 2.06, respectively. The results showed DEFs measured for the same cell lines using (192)Ir brachytherapy to be 1.67 and 1.54 for Du145 and A549 cancer cells, respectively. This clearly indicates that much higher DE values are obtained in the case of eBx™ X-ray brachytherapy compared to (192)Ir gamma brachytherapy. CONCLUSION: The higher DE values obtained with eBx™ compared to (192)Ir brachytherapy can be attributed to the lower average energy of the former and being closer to the optimal energy for DE. This could potentially be utilized by medical practitioners and clinicians to achieve the same tumor control with a significantly lower dose from the eBx™ compared to the (192)Ir brachytherapy treatment, thus bringing huge benefits to the brachytherapy-treated patients. Dove Medical Press 2018-09-25 /pmc/articles/PMC6165788/ /pubmed/30310276 http://dx.doi.org/10.2147/IJN.S174624 Text en © 2018 Shahhoseini et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Shahhoseini, Elham Ramachandran, Prabhakar Patterson, William Roy Geso, Moshi Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title | Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title_full | Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title_fullStr | Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title_full_unstemmed | Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title_short | Determination of dose enhancement caused by AuNPs with Xoft(®) Axxent(®) Electronic (eBx™) and conventional brachytherapy: in vitro study |
title_sort | determination of dose enhancement caused by aunps with xoft(®) axxent(®) electronic (ebx™) and conventional brachytherapy: in vitro study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165788/ https://www.ncbi.nlm.nih.gov/pubmed/30310276 http://dx.doi.org/10.2147/IJN.S174624 |
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