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胰岛素壳聚糖纳米粒的制备
引用本文:应晓英,胡富强,袁弘.胰岛素壳聚糖纳米粒的制备[J].中国药学杂志,2003,38(12):936-939.
作者姓名:应晓英  胡富强  袁弘
作者单位:浙江大学药学院药物制剂研究所,浙江,杭州,310031
摘    要: 目的制备胰岛素壳聚糖纳米粒。方法采用酶水解和超滤膜分离技术,得到不同相对分子质量的壳聚糖,由凝胶渗透色谱法测定其相对分子质量;采用溶剂扩散法制备纳米粒,研究纳米粒的空间结构,测定其粒径、表面电位(zeta电位)、模型药物胰岛素包封率及体外释放。结果通过控制酶水解条件,经超滤分离得到3种不同相对分子质量的壳聚糖,凝胶渗透色谱法测得的重均相对分子质量(MW)分别为10 289,41500和101 870。经溶剂扩散法制备得到的壳聚糖纳米粒,呈类圆形球体,粒径分布较窄,且随制备工艺中乙醇加入量的增加、分散用超声次数的增多,以及壳聚糖分子量的降低,粒径变小。壳聚糖纳米粒带正电荷,zeta电位值大于+30 mV。放射免疫法测得的药物包封率为72.66%。在壳聚糖酶存在条件下,前1 h体外释放药物较快,1 h后趋于平稳,并能持续释放6 h。结论选用合适相对分子质量壳聚糖制备胰岛素壳聚糖纳米粒,方法简便,药物包封率高,并有一定的缓释作用。

关 键 词:壳聚糖  相对分子质量  纳米粒  胰岛素  包封率  体外释放
文章编号:1001-2494(2003)12-0936-04
收稿时间:2002-12-12;
修稿时间:2002年12月12

Preparation of insulin-loaded chitosan nanoparticles
YING Xiao-ying,HU Fu-qiang,YUAN Hong.Preparation of insulin-loaded chitosan nanoparticles[J].Chinese Pharmaceutical Journal,2003,38(12):936-939.
Authors:YING Xiao-ying  HU Fu-qiang  YUAN Hong
Affiliation:School of Pharmaceutical Science,Zhejiang University,Hangzhou 310031,China
Abstract:OBJECTIVETo prepare insulin-loaded chitosan nan op articles.METHODSChitosan with different molecular weights w as prepared by enzymatic degradation and ultrafiltration separation.Their molecu lar weights were determined by gel permeation chromatography (GPC).Chitosan nano particles were prepared by solvent diffusion method.Several characteristics of c hitosan nanoparticles such as morphology,particle size,zeta potential,drug entra pment efficiency and drug release in vitro were evaluated.RESULTS Chitosan with three different molecular weights were obtained by contr olling the conditions of enzymatic degradation and ultrafiltration separation.Th e molecular weights of chitosan determined by gel permeation chromatography (GPC ) were 10 289,41 500, 101 870 ,respectively.The chitosan nanoparticles prepare d by solvent diffusion technique showed a spheric shape and exhibited a narrow p article size distribution,and became smaller after increasing the concentration of alcohol in the system or increasing the sonication treatment times.The distri bution of particle size also turned to narrower when using lower molecular weigh t chitosan.Due to the high zeta potentials of chitosan nanoparticle systems (ove r +30 mV),these systems were relatively stable.The average entrapment efficiency of insulin was 72.66% determined by radioimmunoassay.Insulin release from nanop articles in the delivery vehicle containing chitosanase showed a rapid delivery in the initial hour and then became slow in the next five hours.CONCL USIONIt was easy to prepare the insulin-loaded chitosan nanoparticles with chitosan with optional molecular weights.A high envelopment and certain su stained release effect could be obtained.
Keywords:chitosan  molecular  nanoparticles  insulin  entrapmen t efficiency  drug release in vitro
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