无机材料学报 ›› 2014, Vol. 29 ›› Issue (12): 1327-1332.DOI: 10.15541/jim20140167

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纳米羟基磷灰石/壳聚糖复合微球的原位仿生制备及表征

李 健1, 韩志军1, 魏 延1, 牛璐璐1, 刘 宇1, 路国运2, 黄 棣1   

  1. (太原理工大学 1. 力学学院, 材料强度与结构冲击山西省重点实验室; 2. 应用力学与生物医学工程研究所, 太原 030024)
  • 收稿日期:2014-04-03 修回日期:2014-06-12 出版日期:2014-12-20 网络出版日期:2014-11-20
  • 作者简介:李 健(1989–), 女, 硕士研究生. E-mail: 18503512013@163.com
  • 基金资助:
    国家自然科学基金(11372209, 51203028);山西省青年科技基金(2013021014-2);山西省高等学校科技创新项目(2013111)

In situ Biomimetic Fabrication and Characterization of Nano-hydroxyapatite/ Chitosan Composite Microspheres

LI Jian1, HAN Zhi-Jun1, WEI Yan1, NIU Lu-Lu1, LIU Yu1, LU Guo-Yun2, HUANG Di1   

  1. (1. College of Mechanics, Shanxi Key Laboratory of Material Strength & Structural Impact, Taiyuan University of Technology, Taiyuan 030024, China; 2. Institute of Applied Mechanics & Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China)
  • Received:2014-04-03 Revised:2014-06-12 Published:2014-12-20 Online:2014-11-20
  • About author:LI Jian. E-mail: 18503512013@163.com
  • Supported by:
    National Natural Science Foundation of China (11372209, 51203028);Natural Science Foundation of Shanxi Province (2013021014-2);Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (2013111)

摘要:

为解决纳米羟基磷灰石/壳聚糖(nHA/CS)复合微球中nHA团聚及分散不均的问题, 本研究在油包水的乳液体系中, 原位仿生制备了nHA/CS复合微球, 并与共混法制备的nHA/CS复合微球进行了对比研究。利用扫描电镜(SEM)、X射线能谱(EDS)、X射线衍射(XRD)、红外(FTIR)和激光粒度仪等手段对不同微球的理化性能进行表征。结果表明: 相比共混法, 原位仿生制备的nHA/CS复合微球形态圆整均匀, 分散性好, 粒径分布较窄, 平均粒径为8.62 μm, nHA晶体均匀分布在微球内部及表面, 并与CS基质以化学键结合。该复合微球有望用于骨组织工程及药物控制释放。

关键词: 原位仿生, 纳米羟基磷灰石, 壳聚糖, 复合微球

Abstract:

To solve the problem that nano-hydroxyapatite (nHA) crystals aggregation and non-uniformly distribution in nano-hydroxyapatite/chitosan (CS) composite microspheres, nHA/CS microspheres were prepared through in situ biomimetic method in water-in-oil (W/O) emulsions. The physical and chemical properties of the composite microspheres were investigated by scanning electronic microscopy (SEM), X-ray energy-dispersive spectroscope (EDS), X-ray diffraction (XRD), fourier transform infrared spectroscope (FTIR) and laser particle size analyzer. The results indicate that the composite microspheres are spherical with average size of 8.62 μm and disperse uniformly. Moreover, the nHA crystals are dispersed uniformly within composite microspheres and bonded with CS matrix. The composite microspheres have great potential in bone tissue engineering and drug delivery system.

Key words: in situ biomimetic, nano-hydroxyapatite, chitosan, composite microspheres

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