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Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy
BACKGROUND: Sonodynamic therapy (SDT) is a burgeoning modality for cancer therapy owing to its high tissue-penetrating capability, controllability and safety. Whereas, the undesirable reactive oxygen species (ROS) yield of sonosensitizers and tumor hypoxia are two vulnerable spots of SDT. Therefore,...
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/PMC9003983/ https://www.ncbi.nlm.nih.gov/pubmed/35413839 http://dx.doi.org/10.1186/s12951-022-01398-6 |
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author | Qiao, Xiaohui Xue, Liyun Huang, Hui Dai, Xinyue Chen, Yu Ding, Hong |
author_facet | Qiao, Xiaohui Xue, Liyun Huang, Hui Dai, Xinyue Chen, Yu Ding, Hong |
author_sort | Qiao, Xiaohui |
collection | PubMed |
description | BACKGROUND: Sonodynamic therapy (SDT) is a burgeoning modality for cancer therapy owing to its high tissue-penetrating capability, controllability and safety. Whereas, the undesirable reactive oxygen species (ROS) yield of sonosensitizers and tumor hypoxia are two vulnerable spots of SDT. Therefore, it is an advisable strategy to augment ROS level and simultaneously relieve hypoxia for SDT to arrive its full potential in cancer treatment. RESULTS: In this work, the defected two-dimensional (2D) Pd/H-TiO(2) nanosheets (NSs) with triple antineoplastic properties were dexterously elaborated and engineered using a facile one-pot Pd-catalyzed hydrogenation tactic by loading a tiny amount of Pd and then inletting hydrogen flow at atmospheric pressure and temperature. The 2D black Pd/H-TiO(2) NSs with oxygen defects exerted eximious SDT effect based on the decreased bandgap that made it easier for the separation of electrons and holes when triggered by ultrasound as theoretically guided by density functional theory calculations. Additionally, Pd/H-TiO(2) NSs could serve as Fenton-like agents because of the presence of oxygen defects, facilitating the conversion of hydrogen peroxide into hydroxyl radicals for exerting the chemodynamic therapy (CDT). Simultaneously, the introduced tiny Pd component possessed catalase-like activity responsible for oxygen production to ameliorate hypoxic condition and thus contributed to improving SDT and CDT efficacies. Both in vitro and in vivo results provided compelling evidences of high ROS yield and aggrandized sono-chemodynamic effect of Pd/H-TiO(2) nanosonosensitizers with the detailed underlying mechanism investigation by RNA sequencing. CONCLUSION: This work delves the profound potential of Pd-catalyzed hydrogenated TiO(2) on oncotherapy, and the effective antineoplastic performance and ignorable therapeutic toxicity make it a powerful competitor among a cornucopia of nanosonosensitizers. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01398-6. |
format | Online Article Text |
id | pubmed-9003983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90039832022-04-13 Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy Qiao, Xiaohui Xue, Liyun Huang, Hui Dai, Xinyue Chen, Yu Ding, Hong J Nanobiotechnology Research BACKGROUND: Sonodynamic therapy (SDT) is a burgeoning modality for cancer therapy owing to its high tissue-penetrating capability, controllability and safety. Whereas, the undesirable reactive oxygen species (ROS) yield of sonosensitizers and tumor hypoxia are two vulnerable spots of SDT. Therefore, it is an advisable strategy to augment ROS level and simultaneously relieve hypoxia for SDT to arrive its full potential in cancer treatment. RESULTS: In this work, the defected two-dimensional (2D) Pd/H-TiO(2) nanosheets (NSs) with triple antineoplastic properties were dexterously elaborated and engineered using a facile one-pot Pd-catalyzed hydrogenation tactic by loading a tiny amount of Pd and then inletting hydrogen flow at atmospheric pressure and temperature. The 2D black Pd/H-TiO(2) NSs with oxygen defects exerted eximious SDT effect based on the decreased bandgap that made it easier for the separation of electrons and holes when triggered by ultrasound as theoretically guided by density functional theory calculations. Additionally, Pd/H-TiO(2) NSs could serve as Fenton-like agents because of the presence of oxygen defects, facilitating the conversion of hydrogen peroxide into hydroxyl radicals for exerting the chemodynamic therapy (CDT). Simultaneously, the introduced tiny Pd component possessed catalase-like activity responsible for oxygen production to ameliorate hypoxic condition and thus contributed to improving SDT and CDT efficacies. Both in vitro and in vivo results provided compelling evidences of high ROS yield and aggrandized sono-chemodynamic effect of Pd/H-TiO(2) nanosonosensitizers with the detailed underlying mechanism investigation by RNA sequencing. CONCLUSION: This work delves the profound potential of Pd-catalyzed hydrogenated TiO(2) on oncotherapy, and the effective antineoplastic performance and ignorable therapeutic toxicity make it a powerful competitor among a cornucopia of nanosonosensitizers. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01398-6. BioMed Central 2022-04-12 /pmc/articles/PMC9003983/ /pubmed/35413839 http://dx.doi.org/10.1186/s12951-022-01398-6 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 Qiao, Xiaohui Xue, Liyun Huang, Hui Dai, Xinyue Chen, Yu Ding, Hong Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title | Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title_full | Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title_fullStr | Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title_full_unstemmed | Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title_short | Engineering defected 2D Pd/H-TiO(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
title_sort | engineering defected 2d pd/h-tio(2) nanosonosensitizers for hypoxia alleviation and enhanced sono-chemodynamic cancer nanotherapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9003983/ https://www.ncbi.nlm.nih.gov/pubmed/35413839 http://dx.doi.org/10.1186/s12951-022-01398-6 |
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