期刊文献+

负载bFGF的壳聚糖微球制备及其体外缓释性能测定 被引量:1

Preparation and in vitro release properties of bFGF-loaded chitosan microspheres
原文传递
导出
摘要 目的:制备负载碱性成纤维细胞生长因子(bFGF)的壳聚糖微球,并测其体外释药特性。方法:采用乳化交联法制备壳聚糖空白微球,再进行bFGF吸附,制成负载bFGF的壳聚糖微球,并对微球进行扫描电镜观察。ELISA法测定其载药量与包封率,以及bFGF的体外释放情况。并测定壳聚糖空白微球的吸水膨胀率。结果:负载bFGF的壳聚糖微球直径约4μm,载药量为1.06μg/mg,包封率为84.8%。体外释放实验初期释放bFGF速度较快,随后逐渐趋于平缓。壳聚糖空白微球的吸水膨胀率为650%。结论:采用乳化交联法制备包裹bFGF的壳聚糖缓释微球,简单易行,成球性好,得率高,具有良好的缓释效果。 Objective:To prepare basic fibroblast growth factor (bFGF) loaded chitosan microspheres, and to an- alyze the property of controlled release of bFGF in vitro. Methods: Firstly, chitosan blank microspheres were pre- pared with emulsification cross - linking method, then bFGF - loaded chitosan microspheres were prepared by the ch- itosan blank microspheres absorbing bFGF. The microspheres were observed by scanning electron microscopy, and the drug loading, encapsulation efficiency and in vitro controlled release of the bFGF - loaded chitosan microspheres were measured by ELISA. Furthermore, the water absorption expansion rate of microspheres were measured. Results: The mean diameter of the bFGF - loaded chitosan microspheres was about 4 μm, and the drug loading and encapsulation efficiency of the bFGF - loaded chitosan microspheres were 1.06 μg/mg and 84.8% , respectively. The micro- spheres released quickly at initial 12 hours, and then slowed gradually in vitro. The absorbing water expansion rate of the blank microspheres was 650%. Conclusion: Chitosan microspheres encapsulating bFGF prepared by emulsifica- tion cross -linking method exhibit high yield and good controlled -release effect.
出处 《中国卫生检验杂志》 北大核心 2013年第2期265-267,共3页 Chinese Journal of Health Laboratory Technology
基金 国家自然科学基金面上项目(81071467) 浙江省医学重点学科群项目(XKQ-010-001)生物医药重点学科群 浙江省医药卫生科技计划项目(2010KYB001 2011KYA001)
关键词 碱性成纤维细胞生长因子 壳聚糖 缓释微球 体外释放 Basic fibroblast growth factor Chitosan Sustained- release microspheres Release in vitro
  • 相关文献

参考文献11

  • 1Zhao Y, Liu Z, Pan C, et al. Preparation of gelatin microspheres encap- sulated with bFGF for therapeutic angiogenesis in a canine ischemic hind limb [ J ]. J Biomater Sci Polym Ed,2011,22 (4 - 6) :665 - 682. 被引量:1
  • 2Demirdogen B, Elcin AE, Elcin YM. NeoVascularization by bFGF relea- sing hyaluronie acid - gelatin microspheres:in vitro and in vivo studies [ J ]. Growth Factors,2010,28 (6) :426 - 436. 被引量:1
  • 3Kimura Y, Hokugo A, Takamoto T, et al. Regeneration of anterior cruel- ate ligament by biodegradable seaffold combined with local eontrolled release of basic fibroblast growth factor and collagen wrapping[ J]. Tis- sue Eng Part C,2008,14 (1) :47 -57. 被引量:1
  • 4Richardson TP, Peters MC. Polymeric system for dual growth factor de- livery[ J]. Nat Biotechno1,2001,19 (9) : 1029 - 1034. 被引量:1
  • 5Mitra A, Dey B. Chitosan microspheres in novel drug delivery systems [J]. Indian J Pharm Sei,2011,73(4) :355 -366. 被引量:1
  • 6Shavi GV, Nayak UY, Reddy MS, et al. Sustained release optimized formulation of anastrozole - loaded chitosan microspheres: in vitro and in vivo evaluation [ J ]. J Mater Sci Mater Med, 2011,22 ( 4 ) : 865 - 878. 被引量:1
  • 7Ochiuz L, Peris JE. Preparation and characterisation of alendronate - loaded chitosan microparticles obtained through the spray drying tech- nique[J]. Med Chem. 2009,5(2) :191 - 196. 被引量:1
  • 8Li FQ,Ji RR,Chen X, et al. Cetirizine dihydrochloride loaded microparti- cles design using ionotropic cross -linked chitesan nanoparticles by spray - drying method[J]. Arch Pharm Res,2010,32(12) :1967 - 1973. 被引量:1
  • 9Zeng W,Huang J,Hu X,et al. Ionically cross - linked chitosan micro- spheres for controlled release of bioactive nerve growth factor[ J]. Int J Pharm,2011,421 (2) :283 -290. 被引量:1
  • 10Calvo P, Remufian - Lopez C, Vila - Jato JL, et al. Novel hydro- philic chitosan - polyethylene oxide nanoparticles as protein carriers [ J]. Journal of Applied Polymer Science, 1997,63 ( 1 ) : 125 - 132. 被引量:1

二级参考文献10

共引文献11

同被引文献8

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部