期刊文献+

壳聚糖修饰的神经毒素纳米粒的制备及体外释放研究

Preparation and in vitro release of neurotoxin-loaded PLA nanoparticles modified with chitosan
下载PDF
导出
摘要 目的:制备粒径小、形态均匀、包封率较高、带稳定正电荷的神经毒素纳米粒并研究其体外释放行为。方法:选用聚乳酸为载体,壳聚糖为修饰物,采用复乳法制备神经毒素纳米粒,在单因素试验的基础上结合正交试验优化纳米粒的制备工艺,并对其体外释药特性进行研究。结果:采用优化方法制备的纳米粒粒径较小(140.5nm),形态规则,大小均匀,包封率高(83.5%),Zeta电位为+30.5mV;体外释药行为符合Weibull方程。结论:建立的制备工艺可行,所得纳米粒包封率高,大小均匀,体外释药具有明显的缓释特征。 Aim: To prepare the neurotoxin chitosan-modified PLA nanoparticles with small diameter, good mor- phology, high drug-loading encapsulation efficiency and positive Zeta potential. Methods: The nanoparticles were prepared with PLA and ehitosan by the double-emulsion method, and the orthogonal design was used to optimize the processing parameters, and a preliminary study on the drug release in vitro was made. Results: It was found that the prepared nanoparticles had small particle ( 140. 5 nm) and good morphology with high encapsulation effi- ciency (83.5%) and positive Zeta potential of + 30. 5 mV. In vitro release profile of the nanoparticles was best fitted to Weibull equation. Conclusion: The established method is practicable in the preparation of neurotoxin chitosan-modified PLA nanoparticles with high encapsulation efficiency, narrow range of the particle size distribution, and notable sustained-release in vitro.
出处 《中国药科大学学报》 CAS CSCD 北大核心 2009年第2期116-119,共4页 Journal of China Pharmaceutical University
基金 国家自然科学基金资助项目(No.30371781 No.30772793) 浙江省卫生高层次创新人才培养工程~~
关键词 神经毒素 纳米粒 壳聚糖 复乳法 体外释放 neurotoxin nanoparticles ehitosan double-emulsion method in vitro release
  • 相关文献

参考文献9

  • 1程巧鸳,李范珠.神经毒素纳米粒大鼠鼻腔给药的脑药物动力学研究[J].中国药科大学学报,2007,38(1):77-79. 被引量:15
  • 2Phui Yee JS, Nanling G, Afifiyan F, et al. Snake postsynaptic neurotoxins : gene structure, phylogeny and application in research and therapy[J]. Biochimie,2004,86(2) :137 -149.
  • 3Toblo M, S6nchez A, Vila A,et al. The role of PEG on the stability in digestive fluids and in vivo fate of PEG-PLA nanoparticles following oral administration [ J ] . Colloid Sulf B Biointerfaces, 2000,18(3-4) : 315 -323.
  • 4Behrens l,Pena AIV ,Alonso MJ,et al. Comparative uptake studies of bioadhesive and non-bioadhesive nanoparticles in human intestinal cell lines and rats: the effect of mucus on particle adsorption and transport [ J ]. Pharm Res, 2002,19 ( 8 ) : 1 185 - 1 193.
  • 5Nafee N, Taetz S, Schneider M,et aL Chitosan-coated PLGA nanoparticles for DNA/RNA delivery: effect of the formulation parameters on complexation and transfection of antisense oligonucleotides[ J]. Genetics,2007,3(3) :173 -718.
  • 6Vila A, Samchez A,Tobio M, et al. Design of biodegradable particles for protein delivery [ J ]. J Control Release,2002,78 ( 1-3 ) : 15 - 24.
  • 7杨可伟,李馨儒,杨卓理,刘艳.聚乙二醇接枝壳聚糖聚离子胶束的制备与体外表征研究[J].中国新药杂志,2007,16(13):1030-1034. 被引量:4
  • 8潘宝骏,阙少聪,游明基,田俊,吴小楠.SPSS软件包快速拟合17种曲线模型的方法[J].中国卫生统计,1995,12(4):49-52. 被引量:6
  • 9Tahara K, Sakai T, Yamamoto H, et al. Establishing chltosan coated PLGA nanosphere platform loaded with wide variety of nucleic acid by complexation with cationic compound for gene delivery [ J]. Int J Pharm,2008,354 ( 1-2 ) :210 - 216.

二级参考文献29

  • 1程巧鸳,朱文静,李范珠.鼻腔给药的生物利用度研究进展[J].国外医学(药学分册),2004,31(3):168-172. 被引量:13
  • 2陈汝筑 吴秀荣.眼镜蛇神经毒素的镇痛作用[J].中国药理学通报,1988,4(2):113-117.
  • 3Lu QM,Meng QX,Li DS,et al.Comparative study of three short-chain neurotoxins from the venom of Naja kaouthia(Yunnan,China)[J].J Nat Toxins,2002,11(3):221-229.
  • 4Phui Yee JS,Nanling G,Afifiyan F,et al.Snake postsynaptic neurotoxins:gene structure,phylogeny and application in research and therapy[J].Biochimie,2004,86(2):137-149.
  • 5Paxinos G,Watson C.The rat brain in stereotaxic coordinates[M].Sydney:Academic Press,1997.
  • 6Bagger MA,Bechgard E.The potential of nasal application for delivery to the central brain——a microdialysis study of fluorescein in rats[J].Eur J Pharm Sci,2004,21(2-3):235-242.
  • 7Henriksson J,Tjlve H.Uptake of inorganic mercury in the olfactory bulbs via olfactory pathways in rats[J].Environ Res,1998,77(2):130-140.
  • 8Thorne RG,Emory CR,Ala TA,et al.Quantitative analysis of the olfactory pathway for drug delivery to the brain[J].Brain Res,1995,692(1-2):278-282.
  • 9Illum L.Transport of drugs from the nasal cavity to the central nervous system[J].Eur J Pharm Sci,2000,11(1):1-18.
  • 10Gao X,Tao W,Lu W,et al.Lectin-conjugated PEG-PLA nanoparticles:preparation and brain delivery after intranasal administration[J].Biomaterials,2006,27(18):3 482-3 490.

共引文献22

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