期刊文献+

包埋载药微球的羟基磷灰石/聚氨酯复合组织工程支架的研究 被引量:5

Studies on Hydroxyapatite/Polyurethane Scaffold Containing Drug-loaded Microspheres for Bone Tissue Engineering
下载PDF
导出
摘要 研制具有药物缓释功能的骨组织工程支架,对载药微球包埋于羟基磷灰石/聚氨酯(HA/PU)支架中的药物缓释体系进行了可行性研究.首先将盐酸环丙沙星作为模型药物,包裹于乙基纤维素(EC)微球中,然后将EC微球与HA/PU材料进行复合,制备了抗生素药物缓释支架.结果显示EC微球均匀地分布在HA/PU支架基质中,未对支架的开孔结构和孔隙形貌构成影响.与单纯将药物载入HA/PU支架中相比,复合载药EC微球的HA/PU支架的初期药物暴释明显降低,药物缓释时间延长.体外药物释放实验和抑菌实验结果表明,该载药微球支架具有良好的药物缓释功能和抑菌性能,是一种集骨修复和治疗于一体的新型组织工程支架材料. To explore and develop scaffold for bone regeneration or tissue engineering with the capacity of con-trolled drug delivery,the feasibility of hydroxyapatite/polyurethane(HA/PU) scaffold containing drug-loaded mi-crospheres for controlled drug delivery system was demonstrated.Ciprofloxacin hydrochlorid as a model drug was encapsulated in ethyl cellulose(EC) microspheres,which were subsequently incorporated into HA/PU composite scaffold to generate an antibiotic drug delivery system.The results show that EC microspheres are uniformly dis-tributed in the HA/PU scaffold matrix and display no significant effect on the pore structure of the scaffold.Com-pared with incorporating ciprofloxacin hydrochlorid into scaffolds directly,embedding microspheres into scaffolds significantly reduces the initial burst drug release and extends the release time of drug delivery.In vitro drug deliv-ery tests and antibacterial activity tests prove that drug-loaded microsphere/scaffold system has good drug delivery properties and effective antibacterial properties.These results suggest that the novel drug-loaded microsphere/ scaffold composites developed in this study is a good candidate scaffold with the function of bone repair and infec-tion treatment for bone tissue engineering.
出处 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2011年第10期1073-1077,共5页 Journal of Inorganic Materials
基金 国家863计划项目(2007AA03Z328766) 广州大学新苗计划~~
关键词 聚氨酯 支架 微球 药物缓释 乙基纤维素 polyurethane scaffold microspheres drug delivery ethyl cellulose
  • 相关文献

参考文献17

  • 1Tabata Y. Significance of release technology in tissue engineering. Drug Discovery Today, 2005, 10(23/24): 1639-1646.
  • 2楼伟建,章辉,韩钢.缓慢释放bFGF壳聚糖多孔支架的构建及对细胞生长的影响[J].中国生物医学工程学报,2007,26(3):441-444. 被引量:1
  • 3Habraken W, Wolke J, Mikos A, et al. PLGA microsphere/calcium phosphate cement composites for tissue engineering: in vitro release and degradation characteristics. Journal of Biomaterials Science, Polymer Edition, 2008, 19(9): 1171-1188.
  • 4Liu W, Griffith M, Li F. Alginate microsphere-collagen composite hydrogel for ocular drug delivery and implantation. Journal of Materials Science: Materials in Medicine, 2008, 19(11): 3365-3371.
  • 5Dass C, Walker T, Kalle W, et al. A microsphere-liposome (microplex) vector for targeted gene therapy of cancer. II. In vivo biodistribution study in a solid tumor model. Drug Delivery, 2000, 7(1): 15-19.
  • 6Lee J, Kim S, Kwon I, et al. Effects of a chitosan scaffold containing TGF-β1 encapsulated chitosan microspheres on in vitro chondrocyte culture. Artificial Organs, 2004, 28(9): 829-839.
  • 7Rowe R C, Kotaras A D, White E F T. An evaluation of the plasticizing efficiency of the dialkyl phthalates in ethyl cellulose films using the torsional braid pendulum. International Journal of Parmaceutics, 1984, 22(1): 57-62.
  • 8Porter S C. The effect of additives on the properties of an aqueous film coating. Pharm.Tech., 1980(4): 67-75.
  • 9Hypp-l- R, Husson I, Sundholm F. Evaluation of physical properties of plasticized ethyl cellulose films cast from ethanol solution Part I. International Journal of Pharmaceutics, 1996, 133(1/2): 161-170.
  • 10刘浩怀,张利,左奕,李吉东,邹琴,李玉宝.脂肪族聚氨酯/磷灰石复合材料的原位制备及性能[J].功能材料,2010,41(2):241-244. 被引量:6

二级参考文献38

  • 1郑彩虹,梁文权,虞和永.海藻酸壳聚糖聚乳酸羟乙醇酸复合微球的制备及其对蛋白释放的调节[J].药学学报,2005,40(2):182-186. 被引量:20
  • 2Lamba N M K, Woodhouse K A, Cooper S L. Polyurethanes in Biomedical Applications[M]. New York: CRC Press, 1998.
  • 3Kavlock K, Pechar T, Hollinger J, et al. [J]. Acta Biomaterialia, 2007, 3(4): 475-484.
  • 4Guan J J, Sacks M S, Beckman E J, et al. [J]. J Biomed Mater Res, 2002, 61(3): 493-503.
  • 5Guan J J, Fujimoto K L, Sacks M S, et al. [J]. Biomaterials, 2005, 26(18): 3961-3971.
  • 6Shackelford J F. [J]. Mater Sci Forum, 1999, 293:99 - 106.
  • 7Cerroni L, Filocamo R, Fabbri M, et al. [J]. Biomolecular Engineering, 2002, 19(2-6):119-124.
  • 8Li J D, Zuo Y, Cheng X M, et al. [J]. Materials Research Innovations, 2008, 12(2) : 98-101.
  • 9Li J D, Zuo Y, Cheng X M, et al. [J]. Materials Research Innovations, 2008, 12(2) : 98-101.
  • 10Li Y, Klein CPAT, Meer S, et al. [J]. Journal of Materials Science: Materials in Medicine 1994, 5: 252-255.

共引文献14

同被引文献41

引证文献5

二级引证文献17

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