高等学校化学学报 ›› 2011, Vol. 32 ›› Issue (11): 2574.

• 研究论文 • 上一篇    下一篇

栓塞型新型微包纳药物控释载体的制备及性能

刘源岗1,2, 毛鸿浩1, 王士斌1,2, 孙学战1   

  1. 1.  华侨大学化工学院, 
    2.  生物材料与组织工程研究所, 厦门 361021
  • 收稿日期:2010-11-10 修回日期:2011-07-06 出版日期:2011-11-10 发布日期:2011-10-14
  • 通讯作者: 王士斌 E-mail:sbwang@hqu.edu.cn
  • 基金资助:

    国家“八六三”计划项目(批准号:  2006AA02A118), 国家自然科学基金(批准号: 31000441, 31170939), 中央高校基本科研业务费(批准号: JB-JC1009, JB-SJ1009)及福建省自然科学基金(批准号: 2009J01253, 2011J01223)资助.

Preparation and Characterization of a Novel Embolic Nano-in-Micro Drug Delivery System

LIU Yuan-Gang1,2, MAO Hong-Hao1, WANG Shi-Bin1,2*, SUN Xue-Zhan1   

  1. 1. College of Chemical Engineering, 
    2.  Institute of Biomaterials and Tissue   Engineering, Huaqiao University, Xiamen 361021, China
  • Received:2010-11-10 Revised:2011-07-06 Online:2011-11-10 Published:2011-10-14
  • Contact: WANG Shi-Bin E-mail:sbwang@hqu.edu.cn
  • Supported by:

    国家“八六三”计划项目(批准号:  2006AA02A118), 国家自然科学基金(批准号: 31000441, 31170939), 中央高校基本科研业务费(批准号: JB-JC1009, JB-SJ1009)及福建省自然科学基金(批准号: 2009J01253, 2011J01223)资助.

摘要: 为了抑制药物的突释效应, 减缓药物的释放速率, 实现不同药物的空间分配及顺序释放, 采用乳化法结合高压静电液滴法, 制备了内部包埋有几丁聚糖/海藻酸钙纳米囊的聚精氨酸/几丁聚糖/海藻酸盐微包纳体系(Nano-in-micro drug delivery system, NiM).  通过荧光标记的方法证实了“微包纳”结构并考察了NiM的理化性能.  以牛血清白蛋白及氟尿嘧啶作为药物模型, 考察了聚精氨酸/几丁聚糖/海藻酸盐微包纳体系对单一蛋白类药物和负载两种药物的缓释性能并进行了动力学模型拟合.  结果表明, Ritger-Peppas模型能够较好地模拟该溶胀控释系统的药物释放过程, 与实验结果比较吻合. 同时也证明了该新型载体体系具有无突释、释放速率减缓及顺序释放的功能, 为新型药物载体体系的研究提供了新的思路.

关键词: 微包纳药物释放体系; , 聚精氨酸; , 海藻酸钠; , 几丁聚糖; , 顺序释放

Abstract: A  novel poly-L-arginine/chitosan/calcium alginate nano-in-micro(NiM) drug delivery system was prepared using emulsification combined with electrospraying method. Fluorescent labelling test proved that the nano-in-micro structure of NiM was successfully constructed. Bovine serum albumin(BSA) and 5-FU were used as model drugs and the release profiles of NiM as carriers to a single drug and two different drugs were investigated respectively. The results show that the cumulative release rates are 16.3%(5-FU) and 4.9%(BSA) in 0.5 h, and 82.6%(5-FU) and 10.9%(BSA) after 132 h. Zero-order kinetics, first-order kinetics, Ritger-Peppas model and Higuchi model were used to study the release dynamics of these swelling drug delivery systems and Ritger-Peppas model was proved to be the best one which could fit the experimental data effectively.  It is concluded that the new NiM system can avoid burst release, slow down the release rate and achieve sequential release of different drugs, and it is expected to have potential applications in drug delivery system.

Key words: Nano-in-micro drug delivery system, Poly-L-arginine, Sodium alginate, Chitosan, Sequential release

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