期刊文献+

精氨酸修饰的磁性纳米基因载体的研究 被引量:1

Study on arginine modifying magnetic nanoparticles as gene vector
下载PDF
导出
摘要 采用多层修饰方法制备出精氨酸修饰的磁性纳米基因载体,对样品进行了粒度分析、Zeta电位分析、耐酸性能、生物相容性、体外细胞转染性能研究。结果显示,精氨酸修饰的磁性纳米颗粒均匀,分散性好,大多呈圆球型,平均粒径为15nm,粒径范围10~20nm,其Zeta电位为+29.3mV;多层修饰的纳米磁粒在pH2.0的酸中具有很好的耐酸性能,而未处理的纳米粒子在酸溶液中发生了溶解。MTT实验结果显示,纳米颗粒与细胞有良好的生物相容性;体外细胞转染的结果表明,精氨酸修饰的纳米磁粒能介导pEGFP-N1质粒转染HepC2细胞,并在细胞中表达绿色荧光蛋白。因此,精氨酸修饰的磁性纳米颗粒作为一种新型非病毒基因载体具有介导核酸类生物大分子的应用价值。 An arginine modifying magnetic nanoparticles (AMMN) as gene vector was synthesized by multilay-modifying technique. The AMMN was investigated using granularity analysis, Zeta-potential measurement, acid resistance, biocompatibility and in-vitro transfection. The results showed the morphology of AMMN was mostly spherical and well-distributed,the mean diameter of the nanoparticles was 15 nm and the diameter ranged from 10 ~ 20 nm and its Zeta potential was about + 29.3 mV. These nanoparticles had tremendous durability in acid solution at pH 2.0 while the untreated particles are corroded in acid solution. MTT assay showed the nanoparticles had excellent biocompatibility with cells. The in vitro transfection of AMMN was efficient in HepG2 cells and the expression of green fluorescent proteins was observed under fluorescent microscope. The AMMN may be served as a new-type and effective non-viral carrier for delivery of nueleotides into cells.
出处 《应用化工》 CAS CSCD 2008年第8期844-846,864,共4页 Applied Chemical Industry
基金 国家自然科学基金项目(30671846) 湖南省自然科学基金项目(07jj4008)
关键词 精氨酸 纳米磁粒 基因载体 修饰 arginine magnetic nanoparticles gene vector modifying
  • 相关文献

参考文献11

二级参考文献55

  • 1潘一峰,张阳德,王吉伟,翟登高,王绍闯,王渊璄.PLGA纳米载体介导的端粒酶反义核酸体外转染率及对肝肿瘤细胞的影响[J].中国现代医学杂志,2005,15(23):3540-3543. 被引量:8
  • 2何晓晓,刘芳,王柯敏,葛佳,秦迪岚,龚萍,谭蔚泓.不同功能化基团修饰的硅纳米颗粒与人皮肤角质形成细胞系(HaCaT)的生物效应[J].科学通报,2006,51(10):1156-1162. 被引量:10
  • 3Li Y,Zhang X. PEGylated PLGA nanoparticles as protein carriers:synthesis,preparation and biodistribution in rats.J Control Release,2001;71(2)∶203
  • 4Shirkhanzadeh M. Bioactive calcium phosphate coating prepared by electrodeposition. J Mater Sci Lett, 1991;10∶1415
  • 5Berg K Hansen MB,Nielsen SE. A new sensitive bioassay for precise quantification of interferon activity as measured via the mitochondrial dehydrogenase function in cells (MTT-method). APMIS,1990;98 (2)∶156
  • 6Bloomfield VA. DNA condensation. Curr Opin Struct Biol,1996;6∶334
  • 7Chalfie M. Green fluorescent protein as a marker for gene expression. Science. 1994;263∶802
  • 8Luo D, Saltzman WM. Synthetic DNA delivery systems, Nat Biotechnol,2000;18∶33
  • 9Mosqueira V. C. F, Legrand P, Morgat J,et al. Biodistribution of long-circulating PEG-grafted nanocapsules in mice: effects of PEG chain length and density. Pharm Res, 2001;18∶1411
  • 10Brown WE, Chow LC. A new calcium phosphate, watersetting cement. American Ceramic Society, Ohio, 1987:352-379

共引文献51

同被引文献4

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