...
首页> 外文期刊>Journal of Pharmacy and Pharmacology >Cefuroxime axetil solid dispersions prepared using solution enhanced dispersion by supercritical fluids.
【24h】

Cefuroxime axetil solid dispersions prepared using solution enhanced dispersion by supercritical fluids.

机译:头孢呋辛酯固体分散体是使用溶液通过超临界流体提高分散度而制备的。

获取原文
获取原文并翻译 | 示例
           

摘要

Cefuroxime axetil (CA) solid dispersions with HPMC 2910/PVP K-30 were prepared using solution enhanced dispersion by supercritical fluids (SEDS) in an effort to increase the dissolution rate of poorly water-soluble drugs. Their physicochemical properties in solid state were characterized by differential scanning calorimeter (DSC), powder X-ray diffraction (PXRD), Fourier transform infrared spectrometry (FT-IR) and scanning electron microscopy. No endothermic and characteristic diffraction peaks corresponding to CA were observed for the solid dispersions in DSC and PXRD. FTIR analysis demonstrated the presence of intermolecular hydrogen bonds between CA and HPMC 2910/PVP K-30 in solid dispersions, resulting in the formation of amorphous or non-crystalline CA. Dissolution studies indicated that the dissolution rates were remarkably increased in solid dispersions compared with those in the physical mixture and drug alone. In conclusion, an amorphous or non-crystalline CA solid dispersion prepared using SEDS could be very useful for the formulation of solid dosage forms.
机译:使用HPMC 2910 / PVP K-30的头孢呋辛酯(CA)固体分散体是通过超临界流体(SEDS)的溶液增强分散体制备的,目的是提高水溶性差的药物的溶出度。通过差示扫描量热仪(DSC),粉末X射线衍射(PXRD),傅里叶变换红外光谱(FT-IR)和扫描电子显微镜对它们的固态理化性质进行了表征。对于在DSC和PXRD中的固体分散体,未观察到对应于CA的吸热和特征衍射峰。 FTIR分析表明,固体分散体中CA与HPMC 2910 / PVP K-30之间存在分子间氢键,导致形成非晶或非晶CA。溶出度研究表明,与物理混合物和单独药物相比,固体分散体的溶出度显着提高。总之,使用SEDS制备的非晶态或非晶态CA固体分散体对于固体剂型的配制可能非常有用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号