期刊
MICROPOROUS AND MESOPOROUS MATERIALS
卷 228, 期 -, 页码 318-328出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2016.03.040
关键词
Multi-shelled mesoporous silica nanoparticles (MMSNs); Dual-templating route; Growth mechanism; Catalyst; Drug carrier
类别
资金
- National Natural Science Foundation of China [11275121, 21471096, 21371116]
- Program for Innovative Research Team in University [IRT13078]
A facile vesicle-templating approach has been developed for synthesis of multi-shelled mesoporous silica nanoparticles (MMSNs) through a self-assembly of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl benzene sulfonate (SDBS). The obtained MMSNs displayed a spherical morphology, relatively uniform size distribution with an average diameter of 185 nm and a good biocompatibility. Controlled experiments demonstrated that the morphology and structure of MMSNs were mainly determined by the mass ratio of CTAB/SDBS in the reagents. A possible growth mechanism of MMSNs was proposed based on TEM, SEM, and N-2 sorption analysis, etc. Moreover, the Au-decorated MMSNs (Au@MMSNs) were constructed as the catalyst, which exhibited superior catalytic activity and good cycle stability for the reduction of 4-nitrophenol (4-NP). Additionally, the MMSNs also showed high drug loading efficiency and the controlled pH-responsive release behavior for doxorubicin hydrochloride (DOX). More importantly, the anticancer effect of DOX@MMSNs towards A549 cell further confirmed MMSNs could be employed as an ideal drug carrier. As a consequence, the MMSNs prepared are potential excellent candidates for various applications including nanoreactors, drug delivery, and cancer therapy. (C) 2016 Elsevier Inc. All rights reserved.
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