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Ultrathin gold nanowires to enhance radiation therapy

BACKGROUND: Radiation therapy is a main treatment option for cancer. Due to normal tissue toxicity, radiosensitizers are commonly used to enhance RT. In particular, heavy metal or high-Z materials, such as gold nanoparticles, have been investigated as radiosensitizers. So far, however, the related s...

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Autores principales: Bai, Lin, Jiang, Fangchao, Wang, Renjie, Lee, Chaebin, Wang, Hui, Zhang, Weizhong, Jiang, Wen, Li, Dandan, Ji, Bin, Li, Zibo, Gao, Shi, Xie, Jin, Ma, Qingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488570/
https://www.ncbi.nlm.nih.gov/pubmed/32917209
http://dx.doi.org/10.1186/s12951-020-00678-3
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author Bai, Lin
Jiang, Fangchao
Wang, Renjie
Lee, Chaebin
Wang, Hui
Zhang, Weizhong
Jiang, Wen
Li, Dandan
Ji, Bin
Li, Zibo
Gao, Shi
Xie, Jin
Ma, Qingjie
author_facet Bai, Lin
Jiang, Fangchao
Wang, Renjie
Lee, Chaebin
Wang, Hui
Zhang, Weizhong
Jiang, Wen
Li, Dandan
Ji, Bin
Li, Zibo
Gao, Shi
Xie, Jin
Ma, Qingjie
author_sort Bai, Lin
collection PubMed
description BACKGROUND: Radiation therapy is a main treatment option for cancer. Due to normal tissue toxicity, radiosensitizers are commonly used to enhance RT. In particular, heavy metal or high-Z materials, such as gold nanoparticles, have been investigated as radiosensitizers. So far, however, the related studies have been focused on spherical gold nanoparticles. In this study, we assessed the potential of ultra-thin gold nanowires as a radiosensitizer, which is the first time. METHODS: Gold nanowires were synthesized by the reduction of HAuCl(4) in hexane. The as-synthesized gold nanowires were then coated with a layer of PEGylated phospholipid to be rendered soluble in water. Spherical gold nanoparticles coated with the same phospholipid were also synthesized as a comparison. Gold nanowires and gold nanospheres were first tested in solutions for their ability to enhance radical production under irradiation. They were then incubated with 4T1 cells to assess whether they could elevate cell oxidative stress under irradiation. Lastly, gold nanowires and gold nanoparticles were intratumorally injected into a 4T1 xenograft model, followed by irradiation applied to tumors (3 Gy/per day for three days). Tumor growth was monitored and compared. RESULTS: Our studies showed that gold nanowires are superior to gold nanospheres in enhancing radical production under X-ray radiation. In vitro analysis found that the presence of gold nanowires caused elevated lipid peroxidation and intracellular oxidative stress under radiation. When tested in vivo, gold nanowires plus irradiation led to better tumor suppression than gold nanospheres plus radiation. Moreover, gold nanowires were found to be gradually reduced to shorter nanowires by glutathione, which may benefit fractionated radiation. CONCLUSION: Our studies suggest that gold nanowires are a promising type of radiosensitizer that can be safely injected into tumors to enhance radiotherapy. While the current study was conducted in a breast cancer model, the approach can be extended to the treatment of other cancer types. [Image: see text]
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spelling pubmed-74885702020-09-16 Ultrathin gold nanowires to enhance radiation therapy Bai, Lin Jiang, Fangchao Wang, Renjie Lee, Chaebin Wang, Hui Zhang, Weizhong Jiang, Wen Li, Dandan Ji, Bin Li, Zibo Gao, Shi Xie, Jin Ma, Qingjie J Nanobiotechnology Research BACKGROUND: Radiation therapy is a main treatment option for cancer. Due to normal tissue toxicity, radiosensitizers are commonly used to enhance RT. In particular, heavy metal or high-Z materials, such as gold nanoparticles, have been investigated as radiosensitizers. So far, however, the related studies have been focused on spherical gold nanoparticles. In this study, we assessed the potential of ultra-thin gold nanowires as a radiosensitizer, which is the first time. METHODS: Gold nanowires were synthesized by the reduction of HAuCl(4) in hexane. The as-synthesized gold nanowires were then coated with a layer of PEGylated phospholipid to be rendered soluble in water. Spherical gold nanoparticles coated with the same phospholipid were also synthesized as a comparison. Gold nanowires and gold nanospheres were first tested in solutions for their ability to enhance radical production under irradiation. They were then incubated with 4T1 cells to assess whether they could elevate cell oxidative stress under irradiation. Lastly, gold nanowires and gold nanoparticles were intratumorally injected into a 4T1 xenograft model, followed by irradiation applied to tumors (3 Gy/per day for three days). Tumor growth was monitored and compared. RESULTS: Our studies showed that gold nanowires are superior to gold nanospheres in enhancing radical production under X-ray radiation. In vitro analysis found that the presence of gold nanowires caused elevated lipid peroxidation and intracellular oxidative stress under radiation. When tested in vivo, gold nanowires plus irradiation led to better tumor suppression than gold nanospheres plus radiation. Moreover, gold nanowires were found to be gradually reduced to shorter nanowires by glutathione, which may benefit fractionated radiation. CONCLUSION: Our studies suggest that gold nanowires are a promising type of radiosensitizer that can be safely injected into tumors to enhance radiotherapy. While the current study was conducted in a breast cancer model, the approach can be extended to the treatment of other cancer types. [Image: see text] BioMed Central 2020-09-11 /pmc/articles/PMC7488570/ /pubmed/32917209 http://dx.doi.org/10.1186/s12951-020-00678-3 Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bai, Lin
Jiang, Fangchao
Wang, Renjie
Lee, Chaebin
Wang, Hui
Zhang, Weizhong
Jiang, Wen
Li, Dandan
Ji, Bin
Li, Zibo
Gao, Shi
Xie, Jin
Ma, Qingjie
Ultrathin gold nanowires to enhance radiation therapy
title Ultrathin gold nanowires to enhance radiation therapy
title_full Ultrathin gold nanowires to enhance radiation therapy
title_fullStr Ultrathin gold nanowires to enhance radiation therapy
title_full_unstemmed Ultrathin gold nanowires to enhance radiation therapy
title_short Ultrathin gold nanowires to enhance radiation therapy
title_sort ultrathin gold nanowires to enhance radiation therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488570/
https://www.ncbi.nlm.nih.gov/pubmed/32917209
http://dx.doi.org/10.1186/s12951-020-00678-3
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