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吡喹酮固体脂质纳米粒的研制
引用本文:耿叶慧,杨丽,游劲松,张瑜. 吡喹酮固体脂质纳米粒的研制[J]. 沈阳药科大学学报, 2008, 25(1): 20-23
作者姓名:耿叶慧  杨丽  游劲松  张瑜
作者单位:沈阳药科大学,药学院,辽宁,沈阳,110016
摘    要:目的采用超声分散法制备吡喹酮固体脂质纳米粒,并考察制备过程中的主要影响因素。方法首先通过试验确定制备工艺参数,然后考察各处方因素对粒径大小和稳定性的影响,最后以包封率为评价指标,采用正交实验设计法确定最优处方。结果透射电镜测得纳米粒为类圆球状,粒径分布较均匀。动态光散射法测得样品的粒径为(100±21)nm,包封率为(79.3±0.69)%,平均zeta电位值为-66.3 mV。结论以山嵛酸甘油酯和乙酸丁酯为脂质材料,豆磷脂、泊洛沙姆188和硬脂酸钠为复配乳化剂,采用超声分散法可以简便、快速制得吡喹酮固体脂质纳米粒。

关 键 词:吡喹酮  固体脂质纳米粒  超声分散法
文章编号:1006-2858(2008)01-0020-04
收稿时间:2007-04-06
修稿时间:2007-04-06

Preparation of solid lipid nanoparticles containing praziquantel
GENG Ye-hui,YANG Li,YOU Jin-song,ZHANG Yu. Preparation of solid lipid nanoparticles containing praziquantel[J]. Journal of Shenyang Pharmaceutical University, 2008, 25(1): 20-23
Authors:GENG Ye-hui  YANG Li  YOU Jin-song  ZHANG Yu
Affiliation:School of Pharmacy,Shenyang Pharmaceutical University,Shenyang 110016,China
Abstract:Objective To prepare solid lipid nanoparticles containing praziquantel (PZQ-SLN) by ultrasonic technique,and investigate the main factors in the process of preparing PZQ-SLN.Methods At first the parameters of technology were determined by experiments,then the factors affecting the size and stability of PZQ-SLN were researched. On the basis of the single factor exploration, the satisfactory formulation was selected by orthogonal design with high entrapment efficiency as standard.Results The morphological investigation by transmission electron microscopy showed that the nanoparticles had round and uniform shapes. The mean diameters was(100±21)nm,accordingly the drug entrapment efficiencies was(79.3±0.69)%,and the zeta potential was -66.3 mV. Conclusion The solid lipid nanoparticles loaded with praziquantel can be readily and quickly prepared by ultrasonic technique,with Compritol 888 ATO and butyl acetate as matrix material, soybean lecithin, poloxamer 188 and sodium stearate as co-emulsifier.
Keywords:praziquantel   solid lipid nanoparticles   ultrasonic technique
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