Self-Assembled Metal-Phenolic Networks on Emulsions as Low-Fouling and pH-Responsive Particles

被引:68
作者
Besford, Quinn A. [1 ,2 ]
Ju, Yi [1 ,2 ]
Wang, Ting-Yi [3 ]
Yun, Gyeongwon [1 ,2 ]
Cherepanov, PavelV. [1 ,2 ]
Hagemeyer, Christoph E. [3 ]
Cavalieri, Francesca [1 ,2 ]
Caruso, Frank [1 ,2 ]
机构
[1] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Dept Chem Engn, Parkville, Vic 3010, Australia
[3] Monash Univ, Australian Ctr Blood Dis, NanoBiotechnol Lab, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
drug delivery; emulsion; metal-phenolic networks; nanomaterials; self-assembly; DRUG-DELIVERY; LIPID NANOEMULSIONS; SURFACE-CHEMISTRY; IN-VITRO; NANOPARTICLES; CAPSULES; SIZE; NANOMEDICINE; NANOCARRIERS; RELEASE;
D O I
10.1002/smll.201802342
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Interfacial self-assembly is a powerful organizational force for fabricating functional nanomaterials, including nanocarriers, for imaging and drug delivery. Herein, the interfacial self-assembly of pH-responsive metal-phenolic networks (MPNs) on the liquid-liquid interface of oil-in-water emulsions is reported. Oleic acid emulsions of 100-250 nm in diameter are generated by ultrasonication, to which poly(ethylene glycol) (PEG)-based polyphenolic ligands are assembled with simultaneous crosslinking by metal ions, thus forming an interfacial MPN. PEG provides a protective barrier on the emulsion phase and renders the emulsion low fouling. The MPN-coated emulsions have a similar size and dispersity, but an enhanced stability when compared with the uncoated emulsions, and exhibit a low cell association in vitro, a blood circulation half-life of approximate to 50 min in vivo, and are nontoxic to healthy mice. Furthermore, a model anticancer drug, doxorubicin, can be encapsulated within the emulsion phase at a high loading capacity (approximate to 5 fg of doxorubicin per emulsion particle). The MPN coating imparts pH-responsiveness to the drug-loaded emulsions, leading to drug release at cell internalization pH and a potent cell cytotoxicity. The results highlight a straightforward strategy for the interfacial nanofabrication of pH-responsive emulsion-MPN systems with potential use in biomedical applications.
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页数:9
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