期刊文献+

姜黄素聚合物胶束的制备及体外评价 被引量:4

Preparation of curcumin-loaded polymeric micelles and in vitro evaluation
原文传递
导出
摘要 目的:制备姜黄素的Soluplus聚合物胶束,并对其进行体外评价。方法:采用薄膜分散法制备姜黄素聚合物胶束;采用粒径测定仪、透射电镜、X-射线衍射(XRD)对其进行表征;采用紫外分光光度法测定胶束的包封率和载药量;采用动态膜透析法考察载药胶束的体外释药特性。结果:薄膜分散法制备的胶束呈球形或类球形,平均粒径为(65.54±2.57)nm,平均包封率为(87.73±2.94)%,平均载药量(7.96±2.13)%;XRD结果表明姜黄素以无定型状态或分子状态包载在聚合物胶束中;体外释放结果表明姜黄素的soluplus聚合物胶束具有缓释作用。结论:该胶束制备工艺简单,其粒径、包封率、载药量可控,具有缓释作用。 OBJECTIVE To prepare curcumin-loaded soluplus polymeric micelles(Cur-PMs)and perform evaluation in vitro.METHODS Cur-PMs were prepared by film dispersion method using an amphiphilic copolymer soluplus.The Cur-PMs were characterized by dynamic light scattering,transmission electron microscopy(TEM),X-ray diffraction(XRD).Entrapment efficiency(EE)and drug loading(DL)were determinated by UV.The release curve was determined by dialysis.RESULTSThe Cur-PMs observed by TEM were spherical with a mean particle size of(65.54±2.57)nm,the encapsulation efficiency and drug loading of Cur-PMs were(87.73±2.94)%and(7.96±2.13)%,respectively.X-ray diffraction showed that curcumin was in an amorphous or molecular form in the PMs.Release in vitro showed that Cur-PMs could slow down the release rate.CONCLUSION The preparation process is simple,with controllable particle size,entrapment efficiency and drug loading,and can delay drug release.
出处 《中国医院药学杂志》 CAS CSCD 北大核心 2015年第3期213-216,共4页 Chinese Journal of Hospital Pharmacy
基金 东莞市国际合作(编号:2013508152013) 东莞市医疗卫生科技计划项目(编号:201410515200139) 广东医学院博士启动项目(编号:BS201402) 广东省高校青年创新人才项目(编号:2014LYM0003) 广东医学院面上培育项目(编号:2014)
关键词 姜黄素 Soluplus 聚合物胶束 体外评价 curcumin soluplus polymeric micelles in vitro evaluation
  • 相关文献

参考文献9

  • 1鲍华英,陈荣华.姜黄素的研究进展[J].国外医学(儿科学分册),2003,30(5):254-256. 被引量:90
  • 2王彬辉,章文红,张晓芬,王石健,吴敏,杨赛成.姜黄素的药理及剂型研究进展[J].中华中医药学刊,2013,31(5):1102-1105. 被引量:28
  • 3Hamaguchi T, Matsumura Y, Suzuki M, et al. NK105, a pacli- taxel-incorporating micellar nanoparticle formulation, can ex- tend in vivo antitumor activity and reduce the neurotoxicity of paclitaxel [J]. Brit J Cancer,2005,92(7):1240-1250.
  • 4Nakanishi T,Fukushima S, Okamoto K, et al. Development of the polymer mieelle carrier system for doxorubiein [J]. J Con- trol Release, 2001,74(1 ) : 295-315.
  • 5杨小云.槲皮素聚己内酯-聚乙二醇-聚己内酯嵌段共聚物胶束的研究[D].河南大学硕士学位论文,2007.
  • 6Norris D,Puri N,Sinko P,et al. The effect of physical barriers and properties on the oral absorption of particulates [J]. Adv Drug Delivery Rev, 1998,34(7) : 135-144.
  • 7Monica LA, Afsaneh L A, Glen SK, et al. Amphiphilic blocks copolymers for drug delivery [J]. J Pharm Sci, 2003,92 (7) : 1343-1351.
  • 8Jones MC, Ranger M, Leroux JC,et al. pH-sensitive unimolec- ular polymeric micelles: synthesis of a novel drug carrier [J]. Bioeonjug Chem, 2003,14(4) : 774-782.
  • 9张洪,成蓓.大黄素固体脂质纳米粒的制备及理化性质研究[J].中国药师,2010,13(3):326-329. 被引量:17

二级参考文献64

共引文献131

同被引文献87

  • 1潘显道,王存英.天然抗肿瘤药喜树碱衍生物的研究进展[J].药学学报,2003,38(9):715-720. 被引量:31
  • 2李昕,刘佳佳,何浩,张姿,段承刚,谢华福,何涛.槲皮素对LPS诱导的中性粒细胞产生白介素6的影响[J].免疫学杂志,2006,22(1):40-42. 被引量:28
  • 3李娟,何婕,王广基.银杏酮酯口服前体脂质体的制备及其理化性质[J].中国天然药物,2007,5(3):201-206. 被引量:3
  • 4刘瑞,孟芳,白怀,刘宇,唐承薇,刘秉文.槲皮素、芦丁及葛根素抑制LDL氧化修饰作用的研究[J].中国中药杂志,2007,32(19):2058-2062. 被引量:20
  • 5Reintjes T.Solubility enhancement with BASF pharma polymers solubilizer compendium[M].Lampertheim Germany:Pharma Ingredients&Services,2011:67-72.
  • 6Vasconcelos T,Sarmento B,Costa P.Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs[J].Drug Discov Today,2007,12(23/24):1 068.
  • 7Chokshi RJ,Zia H,Sandhu HK,et al.Improving the dissolution rate of poorly water soluble drug by solid dispersion and solid solution:pros and cons[J].Drug Deliv,2007,14(1):33.
  • 8Chokshi R,Zia H.Hot-melt extrusion technique:a review[J].Iran J Pharm Res,2004,3(1):3.
  • 9Chokshi RJ,Sandhu HK,Iyer RM,et al.Characterization of physico-mechanical properties of indomethacin and polymers to assess their suitability for hot-melt extrusion process as a means to manufacture solid dispersion/solution[J].J Pharm Sci,2005,94(11):2 463.
  • 10Liu JW,Zou MJ,Piao HY,et al.Characterization and pharmacokinetic study of aprepitant solid dispersions with soluplus?[J].Molecules,2015,20(6):11 345.

引证文献4

二级引证文献13

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