Bioinspired Core-Shell Nanoparticles for Hydrophobic Drug Delivery

被引:86
|
作者
Yang, Guangze [1 ]
Liu, Yun [1 ]
Wang, Haofei [1 ]
Wilson, Russell [1 ]
Hui, Yue [1 ]
Yu, Lei [1 ]
Wibowo, David [1 ]
Zhang, Cheng [1 ,2 ]
Whittaker, Andrew K. [1 ,2 ]
Middelberg, Anton P. J. [1 ,3 ]
Zhao, Chun-Xia [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[2] Univ Queensland, Arc Ctr Excellence Convergent Bionano Sci & Techn, St Lucia, Qld 4072, Australia
[3] Univ Adelaide, Fac Engn Comp & Math Sci, Adelaide, SA 5005, Australia
基金
澳大利亚研究理事会;
关键词
biomimetic synthesis; cancer; drug delivery; nanoparticles; peptides; SILICA NANOCAPSULES; MICELLES; IMPROVES;
D O I
10.1002/anie.201908357
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A large range of nanoparticles have been developed to encapsulate hydrophobic drugs. However, drug loading is usually less than 10 % or even 1 %. Now, core-shell nanoparticles are fabricated having exceptionally high drug loading up to 65 % (drug weight/the total weight of drug-loaded nanoparticles) and high encapsulation efficiencies (>99 %) based on modular biomolecule templating. Bifunctional amphiphilic peptides are designed to not only stabilize hydrophobic drug nanoparticles but also induce biosilicification at the nanodrug particle surface thus forming drug-core silica-shell nanocomposites. This platform technology is highly versatile for encapsulating various hydrophobic cargos. Furthermore, the high drug loading nanoparticles lead to better in vitro cytotoxic effects and in vivo suppression of tumor growth, highlighting the significance of using high drug-loading nanoparticles.
引用
收藏
页码:14357 / 14364
页数:8
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