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Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy
Gas‐mediated sonodynamic therapy (SDT) has the potential to become an effective strategy to improve the therapeutic outcome and survival rate of cancer patients. Herein, titanium sulfide nanosheets (TiS (X) NSs) are prepared as cascade bioreactors for sequential gas–sonodynamic cancer therapy. TiS (...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596849/ https://www.ncbi.nlm.nih.gov/pubmed/36026580 http://dx.doi.org/10.1002/advs.202201069 |
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author | Li, Guangqiang Lei, Huali Yang, Yuqi Zhong, Xiaoyan Gong, Fei Gong, Yuehan Zhou, Yangkai Zhang, Yuqi Shi, Haibin Xiao, Zhidong Dong, Zhiqiang Cheng, Liang |
author_facet | Li, Guangqiang Lei, Huali Yang, Yuqi Zhong, Xiaoyan Gong, Fei Gong, Yuehan Zhou, Yangkai Zhang, Yuqi Shi, Haibin Xiao, Zhidong Dong, Zhiqiang Cheng, Liang |
author_sort | Li, Guangqiang |
collection | PubMed |
description | Gas‐mediated sonodynamic therapy (SDT) has the potential to become an effective strategy to improve the therapeutic outcome and survival rate of cancer patients. Herein, titanium sulfide nanosheets (TiS (X) NSs) are prepared as cascade bioreactors for sequential gas–sonodynamic cancer therapy. TiS (X) NSs themselves as hydrogen sulfide (H(2)S) donors can burst release H(2)S gas. Following H(2)S generation, TiS (X) NSs are gradually degraded to become S‐defective and partly oxidized into TiO (X) on their surface, which endows TiS (X) NSs with high sonodynamic properties under ultrasound (US) irradiation. In vitro and in vivo experiments show the excellent therapeutic effects of TiS (X) NSs. In detail, large amounts of H(2)S gas and reactive oxygen species (ROS) can simultaneously inhibit mitochondrial respiration and ATP synthesis, leading to cancer cell apoptosis. Of note, H(2)S gas also plays important roles in modulating and activating the immune system to effectively inhibit pulmonary metastasis. Finally, the metabolizable TiS (X) NSs are excreted out of the body without inducing any significant long‐term toxicity. Collectively, this work establishes a cascade bioreactor of TiS (X) NSs with satisfactory H(2)S release ability and excellent ROS generation properties under US irradiation for programmed gas–sonodynamic cancer therapy. |
format | Online Article Text |
id | pubmed-9596849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95968492022-10-27 Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy Li, Guangqiang Lei, Huali Yang, Yuqi Zhong, Xiaoyan Gong, Fei Gong, Yuehan Zhou, Yangkai Zhang, Yuqi Shi, Haibin Xiao, Zhidong Dong, Zhiqiang Cheng, Liang Adv Sci (Weinh) Research Articles Gas‐mediated sonodynamic therapy (SDT) has the potential to become an effective strategy to improve the therapeutic outcome and survival rate of cancer patients. Herein, titanium sulfide nanosheets (TiS (X) NSs) are prepared as cascade bioreactors for sequential gas–sonodynamic cancer therapy. TiS (X) NSs themselves as hydrogen sulfide (H(2)S) donors can burst release H(2)S gas. Following H(2)S generation, TiS (X) NSs are gradually degraded to become S‐defective and partly oxidized into TiO (X) on their surface, which endows TiS (X) NSs with high sonodynamic properties under ultrasound (US) irradiation. In vitro and in vivo experiments show the excellent therapeutic effects of TiS (X) NSs. In detail, large amounts of H(2)S gas and reactive oxygen species (ROS) can simultaneously inhibit mitochondrial respiration and ATP synthesis, leading to cancer cell apoptosis. Of note, H(2)S gas also plays important roles in modulating and activating the immune system to effectively inhibit pulmonary metastasis. Finally, the metabolizable TiS (X) NSs are excreted out of the body without inducing any significant long‐term toxicity. Collectively, this work establishes a cascade bioreactor of TiS (X) NSs with satisfactory H(2)S release ability and excellent ROS generation properties under US irradiation for programmed gas–sonodynamic cancer therapy. John Wiley and Sons Inc. 2022-08-26 /pmc/articles/PMC9596849/ /pubmed/36026580 http://dx.doi.org/10.1002/advs.202201069 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Li, Guangqiang Lei, Huali Yang, Yuqi Zhong, Xiaoyan Gong, Fei Gong, Yuehan Zhou, Yangkai Zhang, Yuqi Shi, Haibin Xiao, Zhidong Dong, Zhiqiang Cheng, Liang Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title | Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title_full | Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title_fullStr | Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title_full_unstemmed | Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title_short | Titanium Sulfide Nanosheets Serve as Cascade Bioreactors for H(2)S‐Mediated Programmed Gas–Sonodynamic Cancer Therapy |
title_sort | titanium sulfide nanosheets serve as cascade bioreactors for h(2)s‐mediated programmed gas–sonodynamic cancer therapy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596849/ https://www.ncbi.nlm.nih.gov/pubmed/36026580 http://dx.doi.org/10.1002/advs.202201069 |
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