Hydrogel-electrospun fiber composite materials for hydrophilic protein release

被引:69
作者
Han, Ning [1 ]
Johnson, Jed [1 ]
Lannutti, John J. [1 ]
Winter, Jessica O. [1 ]
机构
[1] Ohio State Univ, Dept Biomed Engn, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
Hydrogels; Electrospun fibers; Hydrophilic proteins; PEG; NERVE GROWTH-FACTOR; PHEOCHROMOCYTOMA CELLS; BLOCK-COPOLYMERS; DRUG-DELIVERY; PEG HYDROGELS; DNA DELIVERY; ADHESION; DIFFERENTIATION; SCAFFOLDS; ENHANCE;
D O I
10.1016/j.jconrel.2011.09.094
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although hydrogels are widely used in controlled-release systems, obtaining extended, uniform drug release with little initial burst has been challenging. However, recently researchers have shown that combining hydrogels with another drug delivery material can dramatically improve release kinetics. Here we describe a novel hydrogel-based composite material that exhibits stable, near-linear, sustained release of a model hydrophilic protein (e.g., bovine albumin serum, BSA) for over two months with a significant reduction in initial burst release (7% vs. 20%). The composite is comprised of poly(epsilon-caprolactone) (PCL) electrospun fiber mats coupled with poly(ethylene glycol)-poly(epsilon-caprolactone) diacrylate (PEGPCL) hydrogels through photo-polymerization. It is believed that the additional diffusion barrier provided by hydrophobic electrospun fiber mats reduces hydrogel swelling and water penetration rates and increases the diffusion path length, resulting in delayed, more uniform drug release. Further, released proteins remain bioactive as demonstrated by PC12 cell neurite extension in response to released nerve growth factor (NGF). The use of electrospun fiber mats to modulate hydrogel drug release provides a new method to control release kinetics of hydrophilic proteins, reducing burst release and extending the release duration. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:165 / 170
页数:6
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