Preparation and characterization of gelatin-hydroxyapatite composite microspheres for hard tissue repair

被引:77
作者
Chao, Shao Ching [1 ,2 ,3 ]
Wang, Ming-Jia [1 ]
Pai, Nai-Su [1 ]
Yen, Shiow-Kang [1 ]
机构
[1] Natl Chung Hsing Univ, Dept Mat Sci & Engn, Taichung 40227, Taiwan
[2] Taichung Vet Gen Hosp, Neurol Inst, Dept Minimally Invas Skull Neurosurg, Taichung, Taiwan
[3] Minist Hlth & Welf, ChangHua Hosp, Dept Neurosurg, Changhua 500, Taiwan
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2015年 / 57卷
关键词
Gelatin; Hydroxyapatite; Osteoconductivity; Cell culture; Bioactivity; Biocompatibility; IN-VITRO RELEASE; HYDROTHERMAL SYNTHESIS; BONE REGENERATION; DELIVERY-SYSTEM; GENTAMICIN; COLLAGEN;
D O I
10.1016/j.msec.2015.07.047
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Gelatin-hydroxyapatite composite microspheres composed of 21% gelatin (G) and 79% hydroxyapatite (HA) with uniform morphology and controllable size were synthesized from a mixed solution of Ca(NO3)(2), NH4H2PO4 and gelatin by a wet-chemical method. Material analyses such as X-ray diffraction (XRD), scanning/transmission electron microscopy examination (SEM/TEM) and inductively coupled plasma-mass spectroscopy (ICP-MS) were used to characterize G-HA microspheres by analyzing their crystalline phase, microstructure, morphology and composition. HA crystals precipitate along G fibers to form nano-rods with diameters of 6-10 nm and tangle into porous microspheres after blending. The cell culture indicates that G-HA composite microspheres without any toxicity could enhance the proliferation and differentiation of osteoblast-like cells. In a rat calvarial defect model, G-HA bioactive scaffolds were compared with fibrin glue (F) and Osteoset (R) Bone Graft Substitute (OS) for their capacity of regenerating bone. Four weeks post-implantation, new bone, mineralization, and expanded blood vessel area were found in G-HA scaffolds, indicating greater osteoconductivity and bioactivity than F and OS. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 122
页数:10
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