Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies

被引:186
作者
Arno, Maria C. [1 ]
Inam, Maria [1 ]
Coe, Zachary [1 ]
Cambridge, Graeme [1 ]
Macdougall, Laura J. [1 ]
Keogh, Robert [1 ]
Dove, Andrew P. [1 ]
O'Reilly, Rachel K. [1 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 欧洲研究理事会;
关键词
BLOCK-COPOLYMER MICELLES; CYLINDRICAL MICELLES; DIBLOCK COPOLYMERS; CONTROLLED LENGTH; CRYSTALLINE MICELLES; PARTICLE DESIGN; SINGLE-CRYSTALS; DRUG-DELIVERY; WORM GELS; SHAPE;
D O I
10.1021/jacs.7b10199
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The fabrication of monodisperse nanostructures of highly controlled size and morphology with spatially distinct functional regions is a current area of high interest in materials science. Achieving this control directly in a biologically relevant solvent, without affecting cell viability, opens the door to a wide range of biomedical applications, yet this remains a significant challenge. Herein, we report the preparation of biocompatible and biodegradable poly(epsilon-caprolactone) 1D (cylindrical) and 2D (platelet) micelles in water and alcoholic solvents via crystallization-driven self assembly. Using epitaxial growth in an alcoholic solvent, we show exquisite control over the dimensions and dispersity of these nanostructures, allowing access to uniform morphologies and predictable dimensions based on the unimer-to-seed ratio. Furthermore, for the first time, we report epitaxial growth in aqueous solvent, achieving precise control over 1D nanostructures in water, an essential feature for any relevant biological application. Exploiting this further, a strong, biocompatible and fluorescent hydrogel was obtained as a result of living epitaxial growth in aqueous solvent and cell culture medium. MC3T3 and A549 cells were successfully encapsulated, demonstrating high viability (>95% after 4 days) in these novel hydrogel materials.
引用
收藏
页码:16980 / 16985
页数:6
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