H2O2-responsive theranostic nanomedicine

被引:54
作者
Yu, Luodan [1 ,2 ]
Chen, Yu [1 ]
Chen, Hangrong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen peroxide (H2O2); H2O2; responsibility; Stimuli-responsive; Nanomedicine; Theranostic; HYPOXIA-INDUCIBLE FACTORS; OXIDATIVE STRESS; TUMOR HYPOXIA; PHOTODYNAMIC THERAPY; HYDROGEN-PEROXIDE; REACTIVE OXYGEN; DRUG-DELIVERY; ALZHEIMERS-DISEASE; MESOPOROUS SILICA; CONTROLLED-RELEASE;
D O I
10.1016/j.cclet.2017.05.023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The fast progress of stimuli-responsive theranostic nanomedicine can achieve the specific and high-performance diagnosis and therapy of various diseases. Especially, H2O2-responsive theranostic nanomedicine is recently emerging as a new stimuli-responsive modality showing the great potential for the theranostic of diseases with overexpressed H2O2 because H2O2 is associated with several kinds of human diseases as the most stable and abundant reactive oxygen species. This review summarizes and discusses the very-recent developments of H2O2-responsive theranostic nanoplatforms for versatile biomedical applications, including diagnostic imaging, attenuating tumor hypoxia, enhancing the therapeutic efficiency of photodynamic therapy/radiation therapy/chemotherapy and theranostic of inflammation/diabetic. The facing challenges and future developments of H2O2-responisve theranostics are also briefly discussed to further promote the clinical translation of this new responsive theranostic modality. It is highly believed that H2O2-responsive theranostic nanomedicine will be extensively developed a new specific and efficient theranostic modality to benefit the personalized biomedicine in the near future. (C) 2017 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1841 / 1850
页数:10
相关论文
共 111 条
[51]   Targeting Tumor Hypoxia: Suppression of Breast Tumor Growth and Metastasis by Novel Carbonic Anhydrase IX Inhibitors [J].
Lou, Yuanmei ;
McDonald, Paul C. ;
Oloumi, Arusha ;
Chia, Stephen ;
Ostlund, Christina ;
Ahmadi, Ardalan ;
Kyle, Alastair ;
Keller, Ulrich Auf Dem ;
Leung, Samuel ;
Huntsman, David ;
Clarke, Blaise ;
Sutherland, Brent W. ;
Waterhouse, Dawn ;
Bally, Marcel ;
Roskelley, Calvin ;
Overall, Christopher M. ;
Minchinton, Andrew ;
Pacchiano, Fabio ;
Carta, Fabrizio ;
Scozzafava, Andrea ;
Touisni, Nadia ;
Winum, Jean-Yves ;
Supuran, Claudiu T. ;
Dedhar, Shoukat .
CANCER RESEARCH, 2011, 71 (09) :3364-3376
[52]   Multimodality Imaging Probes: Design and Challenges [J].
Louie, Angelique Y. .
CHEMICAL REVIEWS, 2010, 110 (05) :3146-3195
[53]   Activatable Photosensitizers for Imaging and Therapy [J].
Lovell, Jonathan F. ;
Liu, Tracy W. B. ;
Chen, Juan ;
Zheng, Gang .
CHEMICAL REVIEWS, 2010, 110 (05) :2839-2857
[54]   Redox-Activated Manganese-Based MR Contrast Agent [J].
Loving, Galen S. ;
Mukherjee, Shreya ;
Caravan, Peter .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (12) :4620-4623
[55]   The biocompatibility of porous silicon in tissues of the eye [J].
Low, Suet P. ;
Voelcker, Nicolas H. ;
Canham, Leigh T. ;
Williams, Keryn A. .
BIOMATERIALS, 2009, 30 (15) :2873-2880
[56]   Cancer-Targeted Nanotheranostics: Recent Advances and Perspectives [J].
Ma, Yufei ;
Huang, Jie ;
Song, Saijie ;
Chen, Huabing ;
Zhang, Zhijun .
SMALL, 2016, 12 (36) :4936-4954
[57]   FeIII-Doped Two-Dimensional C3N4 Nanofusiform: A New O2-Evolving and Mitochondria-Targeting Photodynamic Agent for MRI and Enhanced Antitumor Therapy [J].
Ma, Zhifang ;
Zhang, Mengchao ;
Jia, Xiaodan ;
Bai, Jing ;
Ruan, Yudi ;
Wang, Chao ;
Sun, Xuping ;
Jiang, Xiue .
SMALL, 2016, 12 (39) :5477-5487
[58]   Bioresponsive, Cell-Penetrating, and Multimeric MR Contrast Agents [J].
Major, Jody L. ;
Meade, Thomas J. .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (07) :893-903
[59]   Transcriptional regulation of vascular endothelial cell responses to hypoxia by HIF-1 [J].
Manalo, DJ ;
Rowan, A ;
Lavoie, T ;
Natarajan, L ;
Kelly, BD ;
Ye, SQ ;
Garcia, JGN ;
Semenza, GL .
BLOOD, 2005, 105 (02) :659-669
[60]   Origin and physiological roles of inflammation [J].
Medzhitov, Ruslan .
NATURE, 2008, 454 (7203) :428-435