Mesoporous silica-based versatile theranostic nanoplatform constructed by layer-by-layer assembly for excellent photodynamic/chemo therapy

被引:171
作者
Chen, Wei-Hai [1 ,2 ]
Luo, Guo-Feng [1 ,2 ]
Qiu, Wen-Xiu [1 ,2 ]
Lei, Qi [1 ,2 ]
Liu, Li-Han [1 ,2 ]
Wang, Shi-Bo [1 ,2 ,3 ]
Zhang, Xian-Zheng [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Inst Adv Studies, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesoporous silica nanoparticle; Tumor-target; Supramolecular photosensitizer; Dual-modal imaging; Photodynamic/chemo therapy; DRUG-DELIVERY; HYALURONIC-ACID; SINGLET OXYGEN; CANCER-THERAPY; TUMOR; NANOPARTICLES; PHOTOSENSITIZER; PORPHYRIN; WATER; CYCLODEXTRIN;
D O I
10.1016/j.biomaterials.2016.11.057
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Supramolecular photosensitizers (supraPSs) have emerged as effective photodynamic therapy (PDT) agents. Here, we propose the assembling capacity of supraPSs as a new strategy to construct theranostic nanoplatform with versatile functions aming at high-performance tumor therapy. By coating tirapazamine (TPZ)-loaded mesoporous silica nanoparticles (MSNs) with layer-by-layer (LbL) assembled multilayer, the versatile nanoplatform (TPZ@MCMSN-Gd3+) was obtained with the formation of supraPSs via host-guest interaction and the chelation with paramagnetic Gd3+. The TPZ@MCMSN-Gd3+ could be specifically uptaken by CD44 receptor overexpressed tumor cells and respond to hyaluronidase (HAase) to trigger the release of therapeutics. As confirmed by in vivo studies, TPZ@MCMSN-Gd3+ showed preferential accumulation in tumor site and significantly inhibited the tumor progression by the collaboration of PDT and bioreductive chemotherapy under NIR fluorescence/MR imaging guidance. Taken together, this supraPSs based strategy paves a new paradigm of the way for the construction of theranostic nanoplatform. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:54 / 65
页数:12
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