您的位置: 专家智库 > >

赵阳

作品数:2 被引量:2H指数:1
供职机构:北京大学医学部药学院分子药剂学与新释药系统北京市重点实验室更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划国家教育部博士点基金更多>>
相关领域:医药卫生更多>>

文献类型

  • 2篇中文期刊文章

领域

  • 2篇医药卫生

主题

  • 1篇PATHWA...
  • 1篇PREPAR...
  • 1篇SIO2
  • 1篇TARGET...
  • 1篇CELLS
  • 1篇CHARAC...
  • 1篇EFFECT
  • 1篇FEBUXO...
  • 1篇H
  • 1篇SOLUBI...
  • 1篇DISSOL...
  • 1篇MODIFI...

机构

  • 2篇北京大学

作者

  • 2篇张烜
  • 2篇钟婷
  • 2篇张卫强
  • 2篇赵阳
  • 2篇张强
  • 1篇杜若
  • 1篇宋平
  • 1篇姚鑫
  • 1篇黄丹
  • 1篇任伟
  • 1篇郭阳
  • 1篇张爽
  • 1篇王超

传媒

  • 2篇Journa...

年份

  • 1篇2015
  • 1篇2014
2 条 记 录,以下是 1-2
排序方式:
The targeting effect of H_7K(R_2)_2-modified pH-sensitive liposomes on U87-MG cells
2015年
The present study aimed to investigate the targeting effect of H7K(R2)2-modified pH -sensitive liposomes on U87-MG cells. Using coumarin-6 as a fluorescence probe, we prepared H7K(R2)2-modified p H-sensitive liposomes(designated as coumarin-6-PSL-H7K(R2)2). The flow cytometry assay was used to evaluate the effect of H7K(R2)2 proportions on the cellular uptake and endocytosis pathways of coumarin--6--PSL--H7K(R2)2 on U87-MG cells. The circular dichroism(CD) spectroscopy assay was used to investigate the secondary structures of H7K(R2)2 peptide at pH 7.4 and H 6.8, respectively. Our results indicated that the 2.5% proportion of H7K(R2)2 in the coumarin-6--PSL-H7K(R2)2 was superior to those of 1% and 3.5% of H7K(R2)2. The uptake of coumarin--6-PSL--H7K(R2)2 on U87--MG cells was not inhibited by filipin, M-β--CD or chlorpromazine. The secondary structure of H7K(R2)2 at pH 6.8 was mostly presented as β--turn. In conclusion, we suggested that the appropriate proportion of H7K(R2)2 in the H7K(R2)2--modified pH--sensitive liposomes could be set at 2.5%. The cellular uptake pathway for H7K(R2)2-modified pH--sensitive liposomes was via the cell penetrating capacity of H7K(R2)2 which responded to acidic condition. The secondary structure of H7K(R2)2 at pH 6.8, which was presented as the shape of hairpin, might be mainly responsible for its targeting and cell penetrating effect.
赵阳任伟钟婷王超张卫强黄丹张爽郭阳姚鑫张烜张强
The preparation and characteristics of febuxostat SiO2 solid dispersions被引量:2
2014年
In the present research, we selected Sylysia as a porous material and febuxostat(FBT) as model drug to prepare the FBT SiO2 solid dispersions using a solvent evaporation method. We firstly established an HPLC method for determining FBT in our prepared FBT SiO2 solid dispersions. And then, the characteristics of FBT SiO2 solid dispersions were investigated, including differential scanning calorimetry(DSC), powder X-ray diffraction(PXRD), scanning electron microscope(SEM), particle size and distribution. The solubility and dissolution of FBT SiO2 solid dispersion were also evaluated. The results of DSC and PXRD showed that the FBT existed in an amorphous state in FBT SiO2 solid dispersions. The SEM and particle size results indicated that the shape and average particle size of FBT SiO2 solid dispersions was similar to the Sylysia. The solubility and dissolution of FBT in FBT SiO2 solid dispersions were significantly enhanced compared with the pure FBT. In conclusion, we successfully prepared FBT SiO2 solid dispersions to increase the solubility and dissolution rate of the poorly water-soluble FBT.
宋文丁杜若宋平钟婷张卫强赵阳王超张烜张强
关键词:FEBUXOSTAT
共1页<1>
聚类工具0