期刊文献+

超声乳化溶剂蒸发法制备阿奇霉素超细粉体的研究 被引量:1

Preparation of Ultrafine Particles of Azithromycin by Ultrasonic Emulsification-solvent Evaporation Method
在线阅读 下载PDF
导出
摘要 采用超声乳化溶剂蒸发法制备了阿奇霉素超细粉体,讨论了溶剂、温度、稳定剂种类及用量、阿奇霉素浓度等对微粉粒径的影响,优化了实验条件。实验结果表明:在最佳实验条件下(丙酮/水为2/3,阿奇霉素质量浓度为16.33g/L,0.667%聚乙二醇6000,温度为25℃),可制备出平均粒径为1.0μm的均匀分散的阿奇霉素超细粉体;红外分析表明本方法未改变样品的化学结构。 Uhraflne particles of Azidaromycin were produced by ultrasonic emulsifieation- solvent evaporation. The affecting factors including solvent, stabilizer, time and temperature on the average size af the product were studied. The optimal producing condition was that in the presence of PEG6000 of 0.667% at 25℃, the concentration of Azidaromyein was 16.33g/L with the ratio of aeetoned water of 2/3 with aging time of lb. Under the optimal condition, the average size of particles was 1.0μn with the narrow distribution and the chemical structure of Azithro- myein sample was not changed.
出处 《茂名学院学报》 2008年第1期20-23,共4页 Journal of Maoming College
关键词 阿奇霉素 溶剂蒸发 超细粉体 超声乳化 Azithromycin solvem evaporation microparticle ultrasonic emulsification
  • 相关文献

参考文献5

二级参考文献9

  • 1Liversige G G,Cundy K C,Bishop J F,et al. Surface Modified Drug Nanoparticles [P]. US 5145684,1992-09-08.
  • 2Jacobs C,Kayser O,M ller R H. Nanosuspensions as a New Approach for the Formulation for the Poorly Soluble Drug Tarazepide[J]. Int J Pharm,2000,196:161-164.
  • 3Cartensen J T. Solid Pharmaceutics: Mechanical Properties and Rate Phenomena[M].New York:Academic press Inc,1980.
  • 4Liedtke S,Wissing S,Müller R H,et al. Influence of High Pressure Homogenisation Equipment on Nanodispersions Characteristics[J]. Int J Pharm,2000,196:183-185.
  • 5Horn D,Rieger J. Organic Nanoparticles in the Aqueous Phase--Theory, Experiment, and Use Angew[J]. Chem Int Ed,2001,40:4330-4361.
  • 6Murakami H,Kobayashi M,Takeuchi H. Preparation of poly(DL-Lactide-co-Glycolide) Nanoparticles by Modified Spontaneous Emulsification Solvent Diffusion Method [J]. Int J Pharm,1999,187:143-152.
  • 7Lamprecht A,Ubrich N,Yamamoto H,et al. Design of Rolipram-Loaded Nanoparticles:Comparison of Two Preparation Methods[J]. Journal of Controlled Release,2001,(1):297-306.
  • 8Ruch F,Matijevic E. Preparation of Micrometer Size Budesonide Particles by Precipitation[J]. Journal of Colloid and Interface Science,2000,229(1):207-211.
  • 9昝菱,钟家柽,刘忠士.纳米金红石TiO_2粉体的低温制备[J].功能材料,2001,32(3):332-333. 被引量:6

共引文献45

同被引文献13

  • 1龙涛,皮振邦,田熙科,杨力军,张素新.超细阿奇霉素的制备及表征[J].化工进展,2005,24(7):763-766. 被引量:9
  • 2王国联,王洁欣,沈志刚,郭奋,陈建峰,Jimmy Yun.反应沉淀法制备阿奇霉素药物超微粉体[J].过程工程学报,2007,7(4):802-806. 被引量:6
  • 3KATTEBIONAA S,CHANDRASEKHAR P,BALAJI S. Drug Nanocrystals: A Novel Formulation Approach for Poorly Soluble Drugs [J]. International Journal of Pharmteeh Research, 2009,1(3) : 682-686.
  • 4MERISKO-LIVERSIDGE E,LIVERSIDGE G G. Nanosizing for Oral and Parenteral Drug Delivery.. Aperspective on Formulating Poorly-water Soluble Compounds Using Wet Media Milling Technology [j]. Advanced Drug Delivery Reviews, 2011 ,63(6) :27-440.
  • 5EERDENB,RUGH B, VERMANT J ,MARTENS O A, et al, A Screening Study of Surface Stabilization During the Pro- duction of Drug Nanoerystals [J]. Journal of Pharmaceutical Sciences,2009,98(6):2091-2092.
  • 6RONG X Y, XIE Y H, HAO X M,et al. Applications of Polymer Nanocapsules in the Field of Drug Delivery System [J]. Current Drug Discovery Technologies,2011,8(3):173-187,.
  • 7KECK C M, MULLER R H. Drug Nanocrystals of Poorly Soluble Drugs Produced by High Pressure Homogenisation [J]. European Journal of Pharmaceutics and BioIdhsrmaceutics, 2006,62: 3-16.
  • 8夏怡然,王健,朱金屏,等.纳米药物晶体的制备技术研究进晨[J].中国医药工韭杂志,2010,41(2):134-135.
  • 9LIU P, RONG X Y, LAAKSONEN T, et al. Nanosusnsion of Poorly Soluble Drugs : Preparation and Development by Wet Milling [J]. International Journal of Pharmaceutics,2011,411(1-2) :215-222.
  • 10国家药典委员会.中华人民共和冒药典(2部)[M].北京;中凰医药科技出版社,2010.

引证文献1

二级引证文献7

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