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Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy
Introduction: Radiotherapy (RT) is one of the key methods for treating breast cancer. However, the effect of single RT is often poor because of insufficient deposition of X-rays in tumor sites and radiation resistance induced by the abnormal tumor microenvironment (overexpression of glutathione (GSH...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361615/ https://www.ncbi.nlm.nih.gov/pubmed/37485315 http://dx.doi.org/10.3389/fbioe.2023.1225937 |
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author | Wang, Shile Fei, Haotian Ma, Yuhong Zhu, Daoming Zhang, Hongtao Li, Xiang Huang, Qinqin |
author_facet | Wang, Shile Fei, Haotian Ma, Yuhong Zhu, Daoming Zhang, Hongtao Li, Xiang Huang, Qinqin |
author_sort | Wang, Shile |
collection | PubMed |
description | Introduction: Radiotherapy (RT) is one of the key methods for treating breast cancer. However, the effect of single RT is often poor because of insufficient deposition of X-rays in tumor sites and radiation resistance induced by the abnormal tumor microenvironment (overexpression of glutathione (GSH)). The development of multifunctional RT sensitizers and synergetic therapeutic strategies is, therefore, a promising area for enhancing the anticancer effect of RT. Methods: In this study, a multifunctional nanozyme hydrogel based on Cu-doped polypyrrole (CuP) was designed to work concertedly with a second near-infrared thermal RT. The CuP-based hydrogel (CH) reached the tumor site when injected in-situ and achieved long-term storage. Results: Once stimulated with 1064-nm laser irradiation, the heated and softened hydrogel system released CuP nanozyme to provide photothermal therapy, thereby inhibiting the repair of DNA damage caused by RT. In addition, CuP with dual nanozyme activity depleted the intracellular GSH to reduce the antioxidant capacity of the tumor. Moreover, CuP converted H(2)O(2) to produce ·OH to directly kill the tumor cells, thus enhancing the capability of low-dose RT to inhibit tumor growth. In vivo experiments showed that the CH system used in combination with a low-power 1064-nm laser and low-dose RT (4 Gy) exhibited good synergistic anticancer effects and biological safety. Discussion: As a new light-responsive hydrogel system, CH holds immense potential for radio-sensitization. |
format | Online Article Text |
id | pubmed-10361615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103616152023-07-22 Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy Wang, Shile Fei, Haotian Ma, Yuhong Zhu, Daoming Zhang, Hongtao Li, Xiang Huang, Qinqin Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Radiotherapy (RT) is one of the key methods for treating breast cancer. However, the effect of single RT is often poor because of insufficient deposition of X-rays in tumor sites and radiation resistance induced by the abnormal tumor microenvironment (overexpression of glutathione (GSH)). The development of multifunctional RT sensitizers and synergetic therapeutic strategies is, therefore, a promising area for enhancing the anticancer effect of RT. Methods: In this study, a multifunctional nanozyme hydrogel based on Cu-doped polypyrrole (CuP) was designed to work concertedly with a second near-infrared thermal RT. The CuP-based hydrogel (CH) reached the tumor site when injected in-situ and achieved long-term storage. Results: Once stimulated with 1064-nm laser irradiation, the heated and softened hydrogel system released CuP nanozyme to provide photothermal therapy, thereby inhibiting the repair of DNA damage caused by RT. In addition, CuP with dual nanozyme activity depleted the intracellular GSH to reduce the antioxidant capacity of the tumor. Moreover, CuP converted H(2)O(2) to produce ·OH to directly kill the tumor cells, thus enhancing the capability of low-dose RT to inhibit tumor growth. In vivo experiments showed that the CH system used in combination with a low-power 1064-nm laser and low-dose RT (4 Gy) exhibited good synergistic anticancer effects and biological safety. Discussion: As a new light-responsive hydrogel system, CH holds immense potential for radio-sensitization. Frontiers Media S.A. 2023-07-07 /pmc/articles/PMC10361615/ /pubmed/37485315 http://dx.doi.org/10.3389/fbioe.2023.1225937 Text en Copyright © 2023 Wang, Fei, Ma, Zhu, Zhang, Li and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Wang, Shile Fei, Haotian Ma, Yuhong Zhu, Daoming Zhang, Hongtao Li, Xiang Huang, Qinqin Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title | Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title_full | Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title_fullStr | Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title_full_unstemmed | Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title_short | Cu-doped polypyrrole hydrogel with tumor catalyst activity for NIR-II thermo-radiotherapy |
title_sort | cu-doped polypyrrole hydrogel with tumor catalyst activity for nir-ii thermo-radiotherapy |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361615/ https://www.ncbi.nlm.nih.gov/pubmed/37485315 http://dx.doi.org/10.3389/fbioe.2023.1225937 |
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