期刊文献+

改进粒子沥滤法制备PLA径向梯度多孔支架 被引量:2

Preparation of Poly(Lactic Acid) Scaffolds with a Radial Gradient Structure by a Modified Solvent Casting/porgen Leaching Method
下载PDF
导出
摘要 采用溶剂浇铸/真空挥发/粒子沥滤法制备了径向梯度聚乳酸(PLA)多孔支架材料,对支架孔的形貌、孔径、孔隙率、压缩模量及致孔剂和溶剂残留情况等进行了研究.SEM测试结果表明,支架的孔分布均匀,孔径呈现梯度变化,且孔与孔间具有良好的相互连通性.梯度多孔支架各层的平均孔径在(175±30)~(341±23)μm之间;孔隙率均大于(87.9±1.2)%,结果表明:径向各层的孔径、孔隙率可通过致孔剂用量和粒径进行控制.压缩模量在(1.96±0.24)~(2.40±0.1)MPa之间,致孔剂用量和致孔剂粒径的变化均会导致支架力学性能的变化;TGA测试结果证实支架不存在致孔剂和溶剂残留. PLA porous gradient materials were prepared by a solvent casting/vacuum volatilization/porogenleaching (SC/VV/PL) method. The pore morphology, pore size, porosity and compression modulus ofthe scaffolds were studied. The TGA was used to test the quantities of salts and solvent remained insidethe graded scaffold. The results of SEM showed that the scaffold had homogeneous pores distribution, anda better connectivity was found between pores and pores. The average pore sizes of each layer are from 175±30μm to 341±23μm, and the porosity is up to 87.9±1.2%, which showed that each layer's pore sizeand porosity can be controlled by changing the particle size and the amount of the porogen. The compres-sion moduli are between 1.96±0.24MPa and 2.40±0.1MPa. The results of TGA confirmed that therewas no obvious residual of salts and solvent in the resultant scaffolds. This method allows the fabricationof radial grade macroporous PLA scaffold in a simple, homogenous, and fast way.
出处 《湖北工业大学学报》 2012年第1期100-103,共4页 Journal of Hubei University of Technology
基金 国家自然科学基金项目(51173039) 归国留学人员择优资助项目(2008-86)
关键词 溶剂浇铸 多孔支架 梯度材料 solvent casting porous scaffolds gradient materials
  • 相关文献

参考文献12

  • 1Kafri T, Blomer U, Peterson DA, et al. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors.Nat Genet, 1997,17: 314
  • 2Perletti G, Osti D, Marras E, et al. Generation of VSV-G pseudotyped lentiviral particles in 293T cells. J Cell Mol Med, 2004,8:142
  • 3Naldini L, Blomer U, Gage FH, et al. Efficient transfer, integration,and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector. Proc Natl Acad Sci,1996,93:11382
  • 4Kahl CA, Marsh J, Fyffe J, et al. Human immunodeficiency virus type 1-derived lentivirus vectors pseudotyped with envelope glycoproteins derived from Ross River virus and Semliki Forest virus. J Virol, 2004 , 78 :1421
  • 5Wu XY, Wakefield JK, Liu HM, et al. Development of a novel trans-lentiviral vector that affords predictable safety. Mol Ther,2000,2:47
  • 6Abe A, Chen ST, Miyanohara A, et al. In vitro cell-free conversion of noninfectious moloney retrovirus particles to an infectious form by the addition of the vesicular stomatitis virus surrogate envelope G protein. J Virol, 1998,72: 6356
  • 7Curiel DT. High-efficiency gene transfer employing adenoviruspolylysine -DNA complexes. Nat Immun, 1994,13:141
  • 8龚兴厚,邓泽贤,张裕刚,等.一种制备聚合物三维多孔支架的方法:中国,CNl01773682A[P].2010-07-14.
  • 9Naldini L,Blomer U, Gallay P, et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science,1996,272: 263
  • 10Kafri T, Morgan D, Krahl T, et al. Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: Implications for gene therapy. Proc Natl Acad Sci,1998,95:11377

共引文献2

同被引文献14

引证文献2

二级引证文献3

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