2-N, 6-O-sulfated chitosan-assisted BMP-2 immobilization of PCL scaffolds for enhanced osteoinduction

被引:39
作者
Cao, Lingyan [1 ,2 ,3 ,4 ]
Yu, Yuanman [1 ,2 ]
Wang, Jing [1 ,2 ]
Werkmeister, Jerome A. [3 ]
McLean, Keith M. [3 ]
Liu, Changsheng [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Engn Res Ctr Biomed Mat, Minist Educ, Shanghai 200237, Peoples R China
[3] CSIRO Mfg, Bayview Ave, Clayton, Vic 3168, Australia
[4] Shanghai Jiao Tong Univ, Dept Prosthodont, Coll Stomatol, Peoples Hosp 9,Sch Med, 639 Zhizaoju Rd, Shanghai 200011, Peoples R China
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 74卷
基金
中国国家自然科学基金;
关键词
Electrospun; Sulfated chitosan; Bmp-2; Release; Bioactivity; BONE MORPHOGENETIC PROTEIN-2; HEPARIN; HYDROGELS; BEHAVIOR;
D O I
10.1016/j.msec.2016.12.004
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
The aim of this study was to develop a 2-N, 6-O-sulfated chitosan (26SCS) modified electrospun fibrous PCL scaffold for bone morphogenetic protein-2 (BMP-2) delivery to improve osteoinduction. The PCL scaffold was modified by an aminolysis reaction using ethylenediamine (ED) and 26SCS was immobilized via electrostatic interactions (PCL-N-S). Scaffolds were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and contact angle measurements. In vitro BMP-2 adsorption and release kinetics indicated that modified PCL-N-S scaffolds showed higher levels of binding of BMP-2 (about 30-100 times), moderative burst release (about one third), and prolonged releasing time compared to the unmodified PCL scaffold. The bioactivity of released BMP-2 determined by alkaline phosphatase (ALP) activity assay was maintained and improved 8-12 times with increasing concentration of immobilized 26SCS on the scaffolds. In vitro studies demonstrated that bone marrow mesenchymal stem cells (BMSCs) attached more readily to the PCL-N-S scaffolds with increased spreading. In conclusion, 26SCS modified PCL scaffolds can be a potent system for the sustained and bioactive delivery of BMP-2. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:298 / 306
页数:9
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