Multistimuli Responsive Core-Shell Nanoplatform Constructed from Fe3O4@MOF Equipped with Pillar[6]arene Nanovalves

被引:195
作者
Wu, Ming-Xue [1 ]
Gao, Jia [1 ]
Wang, Fang [2 ,3 ,4 ]
Yang, Jie [1 ]
Song, Nan [1 ]
Jin, Xiaoyu [1 ]
Mi, Peng [2 ,3 ,4 ]
Tian, Jian [5 ]
Luo, Jiayan [6 ]
Liang, Feng [7 ]
Yang, Ying-Wei [1 ]
机构
[1] Jilin Univ, Int Joint Res Lab Nanomicro Architecture Chem NMA, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, 2699 Qianjin St, Changchun 130012, Jilin, Peoples R China
[2] Sichuan Univ, Collaborat Innovat Ctr Biotherapy, West China Hosp, State Key Lab Biotherapy, 17 Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, Collaborat Innovat Ctr Biotherapy, West China Hosp, Canc Ctr, 17 Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, Collaborat Innovat Ctr Biotherapy, West China Hosp, Dept Cardiovasc Surg, 17 Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[5] Wuhan Univ, Hubei Prov Engn & Technol Res Ctr Fluorinated Pha, Sch Pharmaceut Sci, Wuhan 430071, Hubei, Peoples R China
[6] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Sch Chem Engn & Technol, Key Lab Green Chem Technol,Minist Educ, Tianjin 300072, Peoples R China
[7] Wuhan Univ Sci & Technol, Sch Chem & Chem Engn, State Key Lab Refractories & Met, Wuhan 430081, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
mechanized metal-organic frameworks; pillarene; supramolecular switches; targeted drug release; Zn2+ triggers; METAL-ORGANIC-FRAMEWORK; MECHANIZED SILICA NANOPARTICLES; ONE-POT SYNTHESIS; DRUG-DELIVERY; SUPRAMOLECULAR NANOVALVES; CONTROLLABLE SYNTHESIS; MAGNETIC-RESONANCE; CANCER; THERAPY; TUMOR;
D O I
10.1002/smll.201704440
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An intelligent theranostic nanoplatform based on nanovalve operated metal-organic framework (MOF) core-shell hybrids, incorporating tumorous microenvironment-triggered drug release, magnetic resonance imaging (MRI) guidance, sustained release, and effective chemotherapy in one pot is reported. The core-shell hybrids are constructed by an in situ growth method, in which Fe3O4 particles with superior abilities of MRI and magnetic separation form the core and UiO-66 MOF with high loading capacity compose the shell, and then are surface-installed with pillararene-based pseudorotaxanes as tightness-adjustable nanovalves. This strategy endows the system with the ability of targeted, multistimuli responsive drug release in response to pH changes, temperature variations, and competitive agents. Water-soluble carboxylatopillar[6]arene system achieved sustained drug release over 7 days due to stronger host-guest binding, suggesting that the nanovalve tightness further reinforces the desirable release of anticancer agent over a prolonged time at the lesion site.
引用
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页数:6
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