Template-Free Synthesis of Chemically Asymmetric Silica Nanotubes for Selective Cargo Loading and Sustained Drug Release

被引:21
|
作者
Deng, Chao [1 ,2 ]
Zhang, Qian [1 ,2 ]
Fu, Cong [1 ,2 ]
Zhou, Fangzhou [1 ,2 ]
Yang, Wuli [3 ]
Yi, Deliang [1 ,2 ]
Wang, Xingdong [4 ]
Tang, Yi [1 ,2 ]
Caruso, Frank [5 ,6 ]
Wang, Yajun [1 ,2 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Fudan Univ, State Key Lab Mol Engn Polymers, Dept Macromol Sci, Shanghai 200433, Peoples R China
[4] CSIRO Mfg, Private Bag 10, Clayton, Vic 3169, Australia
[5] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic, Australia
[6] Univ Melbourne, Dept Chem Engn, Parkville, Vic, Australia
基金
澳大利亚研究理事会; 国家重点研发计划; 澳大利亚国家健康与医学研究理事会; 中国国家自然科学基金;
关键词
MESOPOROUS MATERIALS; SCALE SYNTHESIS; NANOPARTICLES; DELIVERY; SIZE; PERFORMANCE; REDUCTION; NANOWIRES; MEMBRANE; CATALYST;
D O I
10.1021/acs.chemmater.9b01530
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
SiO2 nanotubes (NTs), with uniform diameter (similar to 25 nm) and tailored shell thickness (1-5 nm), and featuring chemically asymmetric surfaces (a silane-functionalized exterior surface and a negatively charged (-Si-O-) interior surface) are prepared by a facile, template-free approach. Owing to their chemically asymmetric properties, positively charged cargoes can be selectively loaded with high content into the SiO2 NTs via electrostatic interaction. Mediated by polyamidoamine dendrimers preassembled in the NTs, different noble metal nanoparticles can be selectively deposited inside the NTs with high density and uniform size. Owing to their high specific surface area and elongated pore structure with lengths up to several micrometers, the SiO2 NTs exhibit a high loading capacity (80 wt %) for positively charged therapeutic agents, which exhibit sustained cargo release properties on the order of several months if the NTs are assembled into a membrane structure.
引用
收藏
页码:4291 / 4298
页数:8
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