Controlled drug release from biodegradable thermoresponsive physical hydrogel nanofibers

被引:194
作者
Loh, Xian Jun [1 ,2 ,3 ]
Peh, Priscilla [1 ]
Liao, Susan [1 ,4 ]
Sng, Colin [3 ]
Li, Jun [1 ,2 ,3 ]
机构
[1] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 117574, Singapore
[2] NUS Grad Sch Integrat Sci & Engn NGS, Singapore 117456, Singapore
[3] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[4] Natl Univ Singapore, Fac Engn, Dept Mech Engn, Singapore 117576, Singapore
关键词
Nanofiber; Hydrogel; Controlled release; Thermosensitive; Block copolymers; Human dermal fibroblast cells; Tissue engineering; TRIBLOCK COPOLYMERIC MICROSPHERES; PROTEIN RELEASE; POLY(ETHYLENE GLYCOL); POLY(ESTER URETHANE)S; IN-VITRO; HYDROLYTIC DEGRADATION; POLY(PROPYLENE GLYCOL); GRAPHITE NANOFIBERS; SUSTAINED-RELEASE; BEHAVIOR;
D O I
10.1016/j.jconrel.2009.12.030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogel nanofiber mats based on thermoresponsive multiblock poly(ester urethane)s comprising poly (ethylene glycol) (PEG), poly(propylene glycol) (PPG), and poly(epsilon-caprolactone) (PCL) segments were fabricated by electrospinning. The hydrogel nanofiber mats were more water absorbent under cold conditions and shrunk when exposed to higher temperatures. The rate of protein release could be controlled by changing the temperature of the nanofiber environment. Cell culture studies on the nanofiber mats were carried out using human dermal fibroblasts, and healthy cell morphology was observed. The adherent viable cells were quantified by MTS after rinsing in excess buffer solution. The results showed that these nanofiber scaffolds supported excellent cell adhesion, comparable with the pure PCL nanofibers. The increased hydrophilicity of these hydrogel nanofiber mats led to a more rapid hydrolytic degradation, compared with the pure PCL nanofiber mats. These hydrogel nanofiber scaffolds could potentially be used as thermoresponsive biodegradable supporting structures for skin tissue engineering applications. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 182
页数:8
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