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Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics

Stimuli‐responsive nanomedicines have become a recent research focus as a candidate for cancer treatment because of their effectiveness, sensibility, and minimal invasiveness. In this work, a novel nanosystem is developed based on Cu(2−) (x)S@MnS core–shell nanoparticles (CSNPs) in which the Cu(2−)...

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Autores principales: Huang, Xiaojuan, Deng, Guoying, Han, Yong, Yang, Guizhu, Zou, Rujia, Zhang, Zhiyuan, Sun, Shuyang, Hu, Junqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794717/
https://www.ncbi.nlm.nih.gov/pubmed/31637173
http://dx.doi.org/10.1002/advs.201901461
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author Huang, Xiaojuan
Deng, Guoying
Han, Yong
Yang, Guizhu
Zou, Rujia
Zhang, Zhiyuan
Sun, Shuyang
Hu, Junqing
author_facet Huang, Xiaojuan
Deng, Guoying
Han, Yong
Yang, Guizhu
Zou, Rujia
Zhang, Zhiyuan
Sun, Shuyang
Hu, Junqing
author_sort Huang, Xiaojuan
collection PubMed
description Stimuli‐responsive nanomedicines have become a recent research focus as a candidate for cancer treatment because of their effectiveness, sensibility, and minimal invasiveness. In this work, a novel nanosystem is developed based on Cu(2−) (x)S@MnS core–shell nanoparticles (CSNPs) in which the Cu(2−) (x)S core serves as a photosensitizer to generate hyperthermia and reactive oxygen species (ROS), and the MnS shell is used in H(2)O(2)‐responsive O(2) production. Cu(2) (−x)S@MnS CSNPs with an independent core and shell ratio are synthesized by a controllable hot‐injection method, resulting in an optimal photothermal (PT) effect with a PT conversion efficiency of up to 47.9%. An enhanced photodynamic (PD) effect also occurs in an H(2)O(2) environment. More significantly, in vivo experiments demonstrate that Cu(2) (−x)S@MnS CSNPs can mediate tumor shrinkage in both HeLa tumor cell line‐derived xenograft (CDX) and head and neck squamous cell carcinoma (HNSCC) patient‐derived xenograft (PDX) models, with the capability of being used as a T1‐enhanced magnetic resonance (MR) contrast agent. These results suggest the great potential of as‐prepared Cu(2) (−x)S@MnS CSNPs as photo/H(2)O(2)‐responsive therapeutic‐agents against tumors, even in a complicated and heterogeneous environment, thus promoting the clinical translation of nanomedicine.
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spelling pubmed-67947172019-10-21 Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics Huang, Xiaojuan Deng, Guoying Han, Yong Yang, Guizhu Zou, Rujia Zhang, Zhiyuan Sun, Shuyang Hu, Junqing Adv Sci (Weinh) Full Papers Stimuli‐responsive nanomedicines have become a recent research focus as a candidate for cancer treatment because of their effectiveness, sensibility, and minimal invasiveness. In this work, a novel nanosystem is developed based on Cu(2−) (x)S@MnS core–shell nanoparticles (CSNPs) in which the Cu(2−) (x)S core serves as a photosensitizer to generate hyperthermia and reactive oxygen species (ROS), and the MnS shell is used in H(2)O(2)‐responsive O(2) production. Cu(2) (−x)S@MnS CSNPs with an independent core and shell ratio are synthesized by a controllable hot‐injection method, resulting in an optimal photothermal (PT) effect with a PT conversion efficiency of up to 47.9%. An enhanced photodynamic (PD) effect also occurs in an H(2)O(2) environment. More significantly, in vivo experiments demonstrate that Cu(2) (−x)S@MnS CSNPs can mediate tumor shrinkage in both HeLa tumor cell line‐derived xenograft (CDX) and head and neck squamous cell carcinoma (HNSCC) patient‐derived xenograft (PDX) models, with the capability of being used as a T1‐enhanced magnetic resonance (MR) contrast agent. These results suggest the great potential of as‐prepared Cu(2) (−x)S@MnS CSNPs as photo/H(2)O(2)‐responsive therapeutic‐agents against tumors, even in a complicated and heterogeneous environment, thus promoting the clinical translation of nanomedicine. John Wiley and Sons Inc. 2019-08-27 /pmc/articles/PMC6794717/ /pubmed/31637173 http://dx.doi.org/10.1002/advs.201901461 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Huang, Xiaojuan
Deng, Guoying
Han, Yong
Yang, Guizhu
Zou, Rujia
Zhang, Zhiyuan
Sun, Shuyang
Hu, Junqing
Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title_full Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title_fullStr Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title_full_unstemmed Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title_short Right Cu(2−) (x)S@MnS Core–Shell Nanoparticles as a Photo/H(2)O(2)‐Responsive Platform for Effective Cancer Theranostics
title_sort right cu(2−) (x)s@mns core–shell nanoparticles as a photo/h(2)o(2)‐responsive platform for effective cancer theranostics
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794717/
https://www.ncbi.nlm.nih.gov/pubmed/31637173
http://dx.doi.org/10.1002/advs.201901461
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