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氟苯尼考β-环糊精包合物的制备 被引量:4

Preparation of florfenicol β-cyclodextrin inclusion complexes
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摘要 为提高氟苯尼考的溶解度和生物利用度,采用饱和水溶液法,以β-环糊精为包合材料制备包合物,通过正交试验对包合条件进行筛选,优选出的最佳包合工艺为包合温度70℃、包合时间5 h、搅拌速度300 r/min;并以扫描电镜、差示扫描量热分析等方法验证氟苯尼考β-环糊精包合物的形成;通过溶出速率法测定,氟苯尼考β-环糊精包合物比氟苯尼考对照品的水溶性提高了6.67倍。 In order to improve the solubility and bioavailability of florfenicol,β-cyclodextrin was used to prepare florfenicolβ-cyclodextrin inclusion complex with saturated aqueous solution method and orthogonal experiment was carried out to optimize the bonding process for inclusion.The results were follows:inclusion time was 5 h with stirring speed of 300 r/min at 70 ℃.In addition,scanning electron microscopy and differential scanning calorimetry analysis were used to verify the formation of florfenicol β-cyclodextrin inclusion complexes.Finally,the solubility of florfenicol β-cyclodextrin inclusion complexes was increased 6.67-fold compared to florfenicol by measuring the rate of dissolution.
机构地区 西南大学药学院
出处 《中兽医医药杂志》 2015年第1期58-62,共5页 Journal of Traditional Chinese Veterinary Medicine
基金 自选课题
关键词 氟苯尼考 Β-环糊精 包合物 florfenicol β-cyclodextrin inclusion complex
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参考文献3

  • 1Masako Oda,Hiroshi Saitoh,Michiya Kobayashi,Bruce J Aungst.β-Cyclodextrin as a suitable solubilizing agent for in situ absorption study of poorly water-soluble drugs[J]. International Journal of Pharmaceutics . 2004 (1)
  • 2R. Graham,D. Palmer,B. C. Pratt,C. A. Hart.In vitro activity of florphenicol[J]. European Journal of Clinical Microbiology & Infectious Diseases . 1988 (5)
  • 3BENDER M L,,KOMIYAMA M.Cyclodextrin reactivi-ty and structure concepts in organic chemistry. Journal of Women s Health . 1978

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