期刊文献+

草乌甲素多囊脂质体包封率的测定 被引量:11

Determination of entrapment efficiency of bulleyaconitine A multivesicular liposomes
下载PDF
导出
摘要 目的:建立测定草乌甲素多囊脂质体包封率的方法。方法:采用离心法分离草乌甲素多囊脂质体,HPLC测定总药量和游离草乌甲素量并计算样品包封率。结果:低速离心时,转速不影响包封率的测定;3批样品的平均包封率为87.12%。结论:离心法操作简单、准确,可用于测定草乌甲素多囊脂质体的包封率。 AIM: To establish a method of determining the entrapment efficiency of bulleyaconitine A multivesicular liposomes. METHODS: Bulleyaconitine muhivesicular liposomes and its free bulleyaconitine were separated by centrifugalization. To calculate the entrapment efficiency, total and free bulleyaconitine were assayed by HPLC. RESULTS: At low speed, the rate of rotation did not affect the determination of entrapment efficiency. The average entrapment efficiency of three lot samples was 87.12%. CONCLUSION: Entrapment efficiency of bulleyaconitine muhivesicular liposomes could be evaluated simply and quickly by centrifugalization.
出处 《中成药》 CAS CSCD 北大核心 2007年第6期825-827,共3页 Chinese Traditional Patent Medicine
关键词 草乌甲素 多囊脂质体 包封率 离心 bulleyaconitine A multivesicular liposomes entrapment efficiency centrifugalization
  • 相关文献

参考文献7

  • 1唐系灿.镇痛抗炎新药滇西都拉碱甲.新药与临床,1986,5(2):120-121.
  • 2唐系灿 刘雪君 陆维华 等.滇西都拉碱甲的镇痛和身体依赖性研究.药学学报,1986,21(12):886-886.
  • 3Kim S,Turker MS,Chi EY,et al.Preparation of multivesieular liposomes[J].Biochem Biophys Acta,1983,728:339-348.
  • 4Sankaram M.A lipid based depot (DepoFoam technology) for sustained release drug delivery[J].Prog Lipid Res,2002,4-4:392-406.
  • 5国家药品标准WS1-(XG-017)-2002
  • 6罗云敬,刘海涛,李天剑,沈含熙.头孢菌素类抗生素脂质体的包封率测定与渗漏研究[J].中国生化药物杂志,1999,20(1):4-6. 被引量:14
  • 7何军,奉建芳,庞家忠,陆伟根,侯世祥.水飞蓟素固体脂质纳米粒载药机制的研究[J].中草药,2004,35(8):864-866. 被引量:4

二级参考文献13

  • 1侯新朴,陶峰,易友云,王文兰.表面带电脂质体载药及对小鼠体内弓形虫的作用[J].药学学报,1989,24(1):53-57. 被引量:14
  • 2徐国兴,谢星辉.三磷酸腺苷脂质体的研究[J].药学学报,1989,24(2):133-138. 被引量:7
  • 3杜鸣.脂质体的性质和应用,山东师范大学硕士学位论文[M].,1988.9-10.
  • 4张林刚,化学学报,1998年,56卷,335页
  • 5温玉麟,国外医药抗生素分册,1990年,11卷,4期,278页
  • 6侯新仆,药学学报,1989年,24卷,1期,53页
  • 7杜鸣,硕士学位论文,1988年,9页
  • 8戚洪,药学学报,1987年,22卷,1期,48页
  • 9M(u)ller R H, Mader K, Gohla S. Solid lipid nanoparticles for controlled drug delivery-a review of the state of the art [J].Eur J Pharm Biopharm, 2000, 50(1): 161-177.
  • 10Muhlen A Z, Schwrz C, Mehnert W. Solid lipid nanoparticles(SLN) for controlled drug delivery-drug release and release mechanism [J]. Eur J Pharm Biopharm, 1998, 45(2): 149-155.

共引文献17

同被引文献113

引证文献11

二级引证文献98

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