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Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy
Radiation therapy is one of the most commonly used methods in clinical cancer treatment, and radiosensitizers could achieve enhanced therapeutic efficacy by incorporating heavy elements into structures. However, the secondary excitation of these high-Z elements-doped nanosensitizers still imply intr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210653/ https://www.ncbi.nlm.nih.gov/pubmed/35729553 http://dx.doi.org/10.1186/s12951-022-01494-7 |
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author | Chen, Lei Zhang, Jinghui Xu, Lihua Zhu, Luchao Jing, Jinpeng Feng, Yushuo Wang, Zongzhang Liu, Peifei Sun, Wenjing Liu, Xiangmei Li, Yimin Chen, Hongmin |
author_facet | Chen, Lei Zhang, Jinghui Xu, Lihua Zhu, Luchao Jing, Jinpeng Feng, Yushuo Wang, Zongzhang Liu, Peifei Sun, Wenjing Liu, Xiangmei Li, Yimin Chen, Hongmin |
author_sort | Chen, Lei |
collection | PubMed |
description | Radiation therapy is one of the most commonly used methods in clinical cancer treatment, and radiosensitizers could achieve enhanced therapeutic efficacy by incorporating heavy elements into structures. However, the secondary excitation of these high-Z elements-doped nanosensitizers still imply intrinsic defects of low efficiency. Herein, we designed Bi-doped titanium dioxide nanosensitizers in which high-Z Bi ions with adjustable valence state (Bi(3+) or Bi(4+)) replaced some positions of Ti(4+) of anatase TiO(2), increasing both X-rays absorption and oxygen vacancies. The as-prepared TiO(2):Bi nanosensitizers indicated high ionizing radiation energy-transfer efficiency and photocatalytic activity, resulting in efficient electron–hole pair separation and reactive oxygen species production. After further modification with cancer cell targeting peptide, the obtained nanoplatform demonstrated good performance in U87MG cell uptakes and intracellular radicals-generation, severely damaging the vital subcellular organs of U87MG cells, such as mitochondrion, membrane lipid, and nuclei etc. These combined therapeutic actions mediated by the composition-tunable nanosensitizers significantly inhibited the U87MG tumor growth, providing a refreshing strategy for X-ray induced dynamic therapy of malignant tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01494-7. |
format | Online Article Text |
id | pubmed-9210653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92106532022-06-22 Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy Chen, Lei Zhang, Jinghui Xu, Lihua Zhu, Luchao Jing, Jinpeng Feng, Yushuo Wang, Zongzhang Liu, Peifei Sun, Wenjing Liu, Xiangmei Li, Yimin Chen, Hongmin J Nanobiotechnology Research Radiation therapy is one of the most commonly used methods in clinical cancer treatment, and radiosensitizers could achieve enhanced therapeutic efficacy by incorporating heavy elements into structures. However, the secondary excitation of these high-Z elements-doped nanosensitizers still imply intrinsic defects of low efficiency. Herein, we designed Bi-doped titanium dioxide nanosensitizers in which high-Z Bi ions with adjustable valence state (Bi(3+) or Bi(4+)) replaced some positions of Ti(4+) of anatase TiO(2), increasing both X-rays absorption and oxygen vacancies. The as-prepared TiO(2):Bi nanosensitizers indicated high ionizing radiation energy-transfer efficiency and photocatalytic activity, resulting in efficient electron–hole pair separation and reactive oxygen species production. After further modification with cancer cell targeting peptide, the obtained nanoplatform demonstrated good performance in U87MG cell uptakes and intracellular radicals-generation, severely damaging the vital subcellular organs of U87MG cells, such as mitochondrion, membrane lipid, and nuclei etc. These combined therapeutic actions mediated by the composition-tunable nanosensitizers significantly inhibited the U87MG tumor growth, providing a refreshing strategy for X-ray induced dynamic therapy of malignant tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01494-7. BioMed Central 2022-06-21 /pmc/articles/PMC9210653/ /pubmed/35729553 http://dx.doi.org/10.1186/s12951-022-01494-7 Text en © The Author(s) 2022 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 Chen, Lei Zhang, Jinghui Xu, Lihua Zhu, Luchao Jing, Jinpeng Feng, Yushuo Wang, Zongzhang Liu, Peifei Sun, Wenjing Liu, Xiangmei Li, Yimin Chen, Hongmin Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title | Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title_full | Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title_fullStr | Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title_full_unstemmed | Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title_short | Composition tunability of semiconductor radiosensitizers for low-dose X-ray induced photodynamic therapy |
title_sort | composition tunability of semiconductor radiosensitizers for low-dose x-ray induced photodynamic therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210653/ https://www.ncbi.nlm.nih.gov/pubmed/35729553 http://dx.doi.org/10.1186/s12951-022-01494-7 |
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