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Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy

BACKGROUND: Nanotechnology in medicine has greatly expanded the therapeutic strategy that may be explored for cancer treatment by exploiting the specific tumor microenvironment such as mild acidity, high glutathione (GSH) concentration and overproduced hydrogen peroxide (H(2)O(2)). Among them, tumor...

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Autores principales: Tang, Wei, Gao, Hongbo, Ni, Dalong, Wang, QiFeng, Gu, Bingxin, He, Xinhong, Peng, Weijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528315/
https://www.ncbi.nlm.nih.gov/pubmed/31109332
http://dx.doi.org/10.1186/s12951-019-0501-3
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author Tang, Wei
Gao, Hongbo
Ni, Dalong
Wang, QiFeng
Gu, Bingxin
He, Xinhong
Peng, Weijun
author_facet Tang, Wei
Gao, Hongbo
Ni, Dalong
Wang, QiFeng
Gu, Bingxin
He, Xinhong
Peng, Weijun
author_sort Tang, Wei
collection PubMed
description BACKGROUND: Nanotechnology in medicine has greatly expanded the therapeutic strategy that may be explored for cancer treatment by exploiting the specific tumor microenvironment such as mild acidity, high glutathione (GSH) concentration and overproduced hydrogen peroxide (H(2)O(2)). Among them, tumor microenvironment responsive chemodynamic therapy (CDT) utilized the Fenton or Fenton-like reaction to produce excess hydroxyl radical (·OH) for the destruction of tumor cells. However, the produced ·OH is easily depleted by the excess GSH in tumors, which would undoubtedly impair the CDT’s efficiency. To overcome this obstacle and enhance the treatment efficiency, we design the nanoplatforms for magnetic resonance imaging (MRI)-guided CDT. RESULTS: In this study, we applied the bovine serum albumin (BSA)-templated CuS:Gd nanoparticles (CuS:Gd NPs) for MRI-guided CDT. The Cu(2+) in the CuS:Gd NPs could be reduced to Cu(+) by GSH in tumors, which further reacted with H(2)O(2) and triggered Fenton-like reaction to simultaneously generate abundant ·OH and deplete GSH for tumor enhanced CDT. Besides, the Gd(3+) in CuS:Gd NPs endowed them with excellent MRI capability, which could be used to locate the tumor site and monitor the therapy process preliminarily. CONCLUSIONS: The designed nanoplatforms offer a major step forward in CDT for effective treatment of tumors guided by MRI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0501-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-65283152019-05-28 Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy Tang, Wei Gao, Hongbo Ni, Dalong Wang, QiFeng Gu, Bingxin He, Xinhong Peng, Weijun J Nanobiotechnology Research BACKGROUND: Nanotechnology in medicine has greatly expanded the therapeutic strategy that may be explored for cancer treatment by exploiting the specific tumor microenvironment such as mild acidity, high glutathione (GSH) concentration and overproduced hydrogen peroxide (H(2)O(2)). Among them, tumor microenvironment responsive chemodynamic therapy (CDT) utilized the Fenton or Fenton-like reaction to produce excess hydroxyl radical (·OH) for the destruction of tumor cells. However, the produced ·OH is easily depleted by the excess GSH in tumors, which would undoubtedly impair the CDT’s efficiency. To overcome this obstacle and enhance the treatment efficiency, we design the nanoplatforms for magnetic resonance imaging (MRI)-guided CDT. RESULTS: In this study, we applied the bovine serum albumin (BSA)-templated CuS:Gd nanoparticles (CuS:Gd NPs) for MRI-guided CDT. The Cu(2+) in the CuS:Gd NPs could be reduced to Cu(+) by GSH in tumors, which further reacted with H(2)O(2) and triggered Fenton-like reaction to simultaneously generate abundant ·OH and deplete GSH for tumor enhanced CDT. Besides, the Gd(3+) in CuS:Gd NPs endowed them with excellent MRI capability, which could be used to locate the tumor site and monitor the therapy process preliminarily. CONCLUSIONS: The designed nanoplatforms offer a major step forward in CDT for effective treatment of tumors guided by MRI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0501-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-20 /pmc/articles/PMC6528315/ /pubmed/31109332 http://dx.doi.org/10.1186/s12951-019-0501-3 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Tang, Wei
Gao, Hongbo
Ni, Dalong
Wang, QiFeng
Gu, Bingxin
He, Xinhong
Peng, Weijun
Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title_full Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title_fullStr Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title_full_unstemmed Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title_short Bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
title_sort bovine serum albumin-templated nanoplatform for magnetic resonance imaging-guided chemodynamic therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528315/
https://www.ncbi.nlm.nih.gov/pubmed/31109332
http://dx.doi.org/10.1186/s12951-019-0501-3
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