Preparation and characterization of electrospun PLGA/gelatin nanofibers as a potential drug delivery system

被引:173
作者
Meng, Z. X. [3 ]
Xu, X. X. [3 ]
Zheng, W. [3 ]
Zhou, H. M. [3 ]
Li, L. [3 ]
Zheng, Y. F. [1 ,3 ]
Lou, X. [2 ,3 ]
机构
[1] Peking Univ, Coll Engn, Dept Adv Mat & Nanotechnol, Beijing 100871, Peoples R China
[2] Curtin Univ Technol, Dept Chem Engn, Bentley, WA 9102, Australia
[3] Harbin Engn Univ, Ctr Biomed Mat & Engn, Harbin 150001, Peoples R China
关键词
Electrospinning; PLGA; Gelatin; Scaffold; Drug delivery; TISSUE ENGINEERING APPLICATIONS; WOUND-DRESSING MATERIALS; ACETATE FIBER MATS; CONTROLLED-RELEASE; POLYMERIC MICELLES; HYDROGEL; GELATIN; SCAFFOLDS; COLLAGEN; BLEND;
D O I
10.1016/j.colsurfb.2010.12.022
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Drug (Fenbufen, FBF)-loaded poly(D,L-lactide-co-glycolide) (PLGA) and PLGA/gelatin nanofibrous scaffolds were fabricated via electrospinning technique. The influences of gelatin content, fiber arrangement, crosslinking time and pH value of the buffer solution on FBF release behavior of the resulting nanofibrous scaffolds were investigated, with the corresponding FBF-loaded PLGA and PLGA/gelatin solvent-cast films as controls. The release rate of FBF was found to be increased with the increment of gelatin content for all the composite samples, and the FBF release rate of aligned nanofibrous scaffold was lower than that of randomly oriented scaffold. Moreover, the crosslinking treatment depressed effectively the burst release of FBF at initial release stage of PLGA/gelatin (9/1) nanofibrous scaffold. In addition, the pH value of the buffer solution could change the physical state of the polymer and affect the FBF release rate. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 102
页数:6
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