期刊
CARBON
卷 183, 期 -, 页码 912-928出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2021.07.073
关键词
Mesoporous materials; Multimorphology; Nanoparticles; Controlled synthesis
资金
- Natural Science Foundation of Guangdong Province [2021A1515010334]
- Science and Technology Planned Project of Guangzhou City [202002030171]
- Key Project for Innovation/Enhancing Guangdong Pharmaceutical University [2019KZDXM048, 2020ZDZX2023]
- Special Funds of Key Disciplines Construction from Guangdong and Zhongshan Cooperating
An emulsion-induced interfacial self-assembly strategy has been developed for the fabrication of mesoporous carbon@mesoporous silica nanoparticles with manipulatable morphology. This method allows for the modulation of the cavity number and location of MC@MSs, transforming the internal structure from hollow to multicavity and flower-like, representing a significant breakthrough.
The remarkable architecture of nanoparticles with anisotropy or hierarchically multicavity mesoporous structure is critical for multifunctional application. However, it is still a great challenge to simultaneously tailor their composition, external morphology and interior structure. Herein, an emulsion-induced interfacial self-assembly strategy has been developed for the first time to fabricate mesoporous carbon@mesoporous silica nanoparticles (MC@MSs) with manipulatable morphology from hollow rambutan-like nanospheres to hollow bowl-like MC@MSs (HBMC@MSs) with different concave degree and surface roughness. Impressively, the cavity number and location of MC@MSs can be modulated, i.e., the evolution of internal structure can be transformed from hollow to multicavity and flower-like by varying the solution polarity of primary emulsion, which is a great breakthrough. A novel swelling-double penetration mechanism is proposed to shed light on the growth kinetics of multimorphology nanoparticles. Moreover, the multifunctional platforms ingeniously overcome three disadvantages: (1) the agglomeration during high-temperature annealing process; (2) low biocompatibility caused by high hydrophobicity; (3) poor affinity with hydrophobic drug molecules. Noticeably, the cellular uptake property of HBMC@MSs with red blood cell biomimetic morphology is more favorable than that of spherical nanoparticles. This strategy endows new understanding of fabricating well-defined MC@MSs and rationally designing the nanomedicine carrier for efficient delivery. (C) 2021 Elsevier Ltd. All rights reserved.
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