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薄膜-超声分散法制备川芎嗪固体脂质纳米粒
饶卫兵1, 郝存江2, 魏丽2, 李发萍2
1.天津中医药大学 天津 300193;2.天津市中药化学与分析重点实验室 天津 300193
摘要:
[目的]制备川芎嗪固体脂质纳米粒,并对其载药量和包封率进行考察。[方法]采用薄膜超声分散法制备,并以包封率为指标采用正交设计法优化川芎嗪固体脂质纳米粒的制备工艺。[结论]所得川芎嗪固体脂质纳米粒的最佳制备处方是川芎嗪30mg,卵磷脂300mg,硬脂酸300mg,30g/L的甘露醇15mL。[结论]该处方可用于川芎嗪固体脂质纳米粒的制备,工艺简单、可行。
关键词:  川芎嗪固体脂质纳米粒  薄膜超声分散法  制备
DOI:10.11656/j.issn.1672-1519.2009.06.26
分类号:
基金项目:
Preparation of ligustrazine solid lipid nanoparticles by film-ultrasonic wave dissolving techniques
RAO Wei-bing,HAO Cun-jiang,WEI Li
Tianjin University of TCM, Tianjin Key Laboratory of Chemistry and Analysis of Chinese Materia Medica, Tianjin 300193, China
Abstract:
[Objective] To prepare the ligustrazine solid lipid nanoparticles and investigate its entrapment efficiency and drug loading. [Methods] The ligustrazine solid lipid nanoparticles were prepared by film ultrasonic wave dissolving techniques. The optimum formula was selected through orthogonal design test according to the entrapment efficiency. [Results] The optimizing technique was using ligustrazine (30 mg),stearic acid (300 mg),lecithin (300 mg),mannitol (30g/L,15 mL). [Conclusion] The preparation technology of ligustrazine solid lipid nanoparticles by film ultrasonic wave dissolving technique is feasible.
Key words:  ligustrazine solid lipid nanoparticles  film ultrasonic wave dissolving technique  preparation
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