Design and synthesis of periodic mesoporous organosilica materials with a multi-compartment structure

被引:3
|
作者
Lin, Chun Xiang Cynthia [1 ]
Jambhrunkar, Siddharth [1 ]
Yuan, Pei [2 ]
Zhou, Chun Hui Clayton [3 ]
Zhao, George Xiu Song [4 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
[2] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[3] Zhejiang Univ Technol, Coll Chem Engn, Res Grp Adv Mat & Sustainable Catalysis AMSC, Hangzhou 310014, Zhejiang, Peoples R China
[4] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
CANCER-CELLS; TARGETED DELIVERY; ORGANIC GROUPS; IN-VITRO; ARTEMISININ; NANOPARTICLES; DERIVATIVES; MICELLES; SILICA; CARRIERS;
D O I
10.1039/c5ra16497d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently many scientists are interested in replicating the unique structure and function of multi-compartments found in natural cells. Despite the success in recreating multi-compartment structures for organic materials, it is a great challenge to translate a similar concept into inorganic and hybrid materials for more versatile applications. Here, as the first example in the organosilica family, we present a facile synthesis route to create hybrid materials with a multi-compartment structure through the spontaneous assembly of fluorocarbon (FC) and hydrocarbon (HC) surfactants with the addition of co-solvent. The formation of multi-compartment periodic mesoporous organosilica (MCPMO) is triggered by the presence of organic co-solvent that induces an osmotic pressure difference in the system. The MCPMO demonstrates a high loading capacity of the antimalarial and anticancer drug artemisinin (47%) with a sustainable release profile attributed to the unique compartmentalized structure and hydrophobic properties. This synthesis strategy can be extended to design various materials with different compositions and morphologies for wider applications including microelectronics, biomedicine, catalysis and energy storage.
引用
收藏
页码:89397 / 89406
页数:10
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