Spatially-controlled distribution of HACC in mineralized collagen coatings for improving rhBMP-2 loading and release behavior

被引:6
|
作者
Chen, Lu [1 ]
Lin, Jun [2 ]
Li, Juan [2 ]
Wang, Xiaozhao [1 ]
Zhuang, Junjun [1 ]
Wang, Huiming [2 ]
Cheng, Kui [1 ]
Weng, Wenjian [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Mineralized collagen coating; Electrochemical deposition; HACC location; rhBMP-2; loading; Cytocompatibility; IN-VITRO; ELECTROCHEMICAL DEPOSITION; CHITOSAN NANOSPHERES; DRUG-DELIVERY; RGD PEPTIDE; TITANIUM; OSSEOINTEGRATION; ANTIBACTERIAL; STABILITY; SCAFFOLDS;
D O I
10.1016/j.colsurfb.2016.04.047
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this study, mineralized collagen (COL) coatings with controlled loading and release of bone morphogenetic protein (rhBMP-2) as well as enhanced osteogenic differentiation were successfully achieved via the spatially-control of hydroxypropyltrimethyl ammonium chloride chitosan (HACC) within the coatings. The distribution of HACC in the inner part (HACC-IN) or the outer part (HACC-OUT) of the coatings were adjusted by different potential values and negative/positive alternations during alternating potentials assisted electrochemical deposition (AP-ECD). It was found that rhBMP-2 loading capacity was remarkably enhanced with the increased incorporation of HACC due to their strong interaction, and the release behavior was also tuned by HACC location. In general, HACC-IN coatings showed a prominent improvement in cytocompatibility and osteogenic differentiation. The main reason is considered that the inner location of HACC can eliminate the negative effect of HACC to initial cellular adhesion and bring to a sustained rhBMP-2 release behavior due to kinetic modification. An optimized coating in this work could load as high as 4644 ng/cm(2) rhBMP-2 and release only 25% for 14 days, which consequently leads to a better osteogenic differentiation. This study has thus inspired another promising protocol for designing growth factor incorporated bioactive coatings for bone implants with improved osteointegration. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:114 / 121
页数:8
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