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Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets
The biodegradability and clearance of metal-based nanomaterials have been questioned worldwide, which have greatly limited their clinical translation. Herein, ultrathin manganese dioxide (MnO(2)) nanosheets with broad near-infrared (NIR) absorption and pH-dependent degradation properties were prepar...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610525/ https://www.ncbi.nlm.nih.gov/pubmed/31257941 http://dx.doi.org/10.1080/10717544.2019.1631409 |
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author | Zeng, Dewang Wang, Lei Tian, Lu Zhao, Shili Zhang, Xianfeng Li, Hongyan |
author_facet | Zeng, Dewang Wang, Lei Tian, Lu Zhao, Shili Zhang, Xianfeng Li, Hongyan |
author_sort | Zeng, Dewang |
collection | PubMed |
description | The biodegradability and clearance of metal-based nanomaterials have been questioned worldwide, which have greatly limited their clinical translation. Herein, ultrathin manganese dioxide (MnO(2)) nanosheets with broad near-infrared (NIR) absorption and pH-dependent degradation properties were prepared. After being modified with polyethylene glycol-cyclic arginine-glycineaspartic acid tripeptide (PEG-cRGD), the MnO(2) nanosheets were then used as photothermal agent and nanocarrier to encapsulate chlorin e6 (Ce6) for targeted photothermal (PTT) and photodynamic (PDT) of cancer. As expected, the MnO(2)-PEG-cRGD nanosheets show high Ce6 loading capacity (351 mg/g), superb photothermal conversion performance (37.2%) and excellent colloidal stability. These nanosheets also exhibit pH-dependent and NIR-induced Ce6 release. Furthermore, the MnO(2) nanosheets can be degraded by reacting with hydrogen peroxide in the acidic microenvironment, which are able to elevate the oxygen concentration in situ and thus reverses the tumor hypoxia. Thanks to these favorable properties and the cRGD-mediated tumor-targeted ability, the fabricated MnO(2)-PEG-cRGD/Ce6 nanocomposites can be effectively up taken by alpha-v beta-3 (α(v)β(3)) integrin over-expressed prostatic carcinoma PC3 cells and achieve favorable therapeutic outcomes under a single 660 nm NIR laser, which is also verified by in vitro studies. The biodegradable MnO(2)-PEG-cRGD/Ce6 nanosheets developed in this work can be a promising nanoplatform for synergetic PTT/PDT cancer therapy. |
format | Online Article Text |
id | pubmed-6610525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-66105252019-07-12 Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets Zeng, Dewang Wang, Lei Tian, Lu Zhao, Shili Zhang, Xianfeng Li, Hongyan Drug Deliv Research Article The biodegradability and clearance of metal-based nanomaterials have been questioned worldwide, which have greatly limited their clinical translation. Herein, ultrathin manganese dioxide (MnO(2)) nanosheets with broad near-infrared (NIR) absorption and pH-dependent degradation properties were prepared. After being modified with polyethylene glycol-cyclic arginine-glycineaspartic acid tripeptide (PEG-cRGD), the MnO(2) nanosheets were then used as photothermal agent and nanocarrier to encapsulate chlorin e6 (Ce6) for targeted photothermal (PTT) and photodynamic (PDT) of cancer. As expected, the MnO(2)-PEG-cRGD nanosheets show high Ce6 loading capacity (351 mg/g), superb photothermal conversion performance (37.2%) and excellent colloidal stability. These nanosheets also exhibit pH-dependent and NIR-induced Ce6 release. Furthermore, the MnO(2) nanosheets can be degraded by reacting with hydrogen peroxide in the acidic microenvironment, which are able to elevate the oxygen concentration in situ and thus reverses the tumor hypoxia. Thanks to these favorable properties and the cRGD-mediated tumor-targeted ability, the fabricated MnO(2)-PEG-cRGD/Ce6 nanocomposites can be effectively up taken by alpha-v beta-3 (α(v)β(3)) integrin over-expressed prostatic carcinoma PC3 cells and achieve favorable therapeutic outcomes under a single 660 nm NIR laser, which is also verified by in vitro studies. The biodegradable MnO(2)-PEG-cRGD/Ce6 nanosheets developed in this work can be a promising nanoplatform for synergetic PTT/PDT cancer therapy. Taylor & Francis 2019-07-01 /pmc/articles/PMC6610525/ /pubmed/31257941 http://dx.doi.org/10.1080/10717544.2019.1631409 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zeng, Dewang Wang, Lei Tian, Lu Zhao, Shili Zhang, Xianfeng Li, Hongyan Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title | Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title_full | Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title_fullStr | Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title_full_unstemmed | Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title_short | Synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable MnO(2) nanosheets |
title_sort | synergistic photothermal/photodynamic suppression of prostatic carcinoma by targeted biodegradable mno(2) nanosheets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610525/ https://www.ncbi.nlm.nih.gov/pubmed/31257941 http://dx.doi.org/10.1080/10717544.2019.1631409 |
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