醋酸氟孕酮载药系统的初步研究
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  • 英文篇名:Preliminary Studies on the Drug Delivery System of Fluocinone Acetate
  • 作者:赵菲 ; 才燕 ; 刘泓 ; 杨升 ; 杨琳燕
  • 英文作者:Zhao Fei;Cai Yan;Liu Hong;Yang Sheng;Yang Linyan;College of Animal Science and Veterinary Medicine,Tianjin Agricultural University;Guangxi Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources,Guangxi Normal University;
  • 关键词:Fe_3O_4@SiO_2-NH_2-PEG ; PEG-FGA ; 紫外-可见分光光度法
  • 英文关键词:Fe_3O_4@SiO_2-NH_2-PEG;;PEG-FGA;;UV-visible spectrophotometry
  • 中文刊名:NKDZ
  • 英文刊名:Acta Scientiarum Naturalium Universitatis Nankaiensis
  • 机构:天津农学院动物科学与动物医学学院;广西师范大学省部共建药用资源化学与药物分子工程国家重点实验室;
  • 出版日期:2019-04-15
  • 出版单位:南开大学学报(自然科学版)
  • 年:2019
  • 期:v.52
  • 基金:国家自然科学基金(31572492);; 天津市教委科研计划项目(2017KJ190);; 省部共建药用资源化学与药物分子工程国家重点实验室资助课题(CMEMR2016-B12)
  • 语种:中文;
  • 页:NKDZ201902019
  • 页数:5
  • CN:02
  • ISSN:12-1105/N
  • 分类号:110-114
摘要
采用化学共沉淀法制备Fe_3O_4纳米粒子(MNPs),对Fe_3O_4MNPs进行无机材料SiO_2包被和氨基化,依次得到Fe_3O_4@SiO_2和Fe_3O_4@SiO_2-NH_2,再对Fe_3O_4@SiO_2-NH_2和醋酸氟孕酮(FGA)进行PEG化,分别得到Fe_3O_4@SiO_2-NH_2-PEG和PEG-FGA产物.分别以20 mg∶20 mg、20 mg∶10 mg的比例进行Fe_3O_4@SiO_2-NH_2-PEG和PEG-FGA的装载研究.最后利用紫外-可见分光光度法对样品装载、释放的结果进行吸光度测定,通过FGA的浓度标准曲线,计算样品的释放浓度.结果表现为在释放过程中,从4-20 d数据结果看,20 mg∶10 mg的样品要好于20 mg∶20 mg的样品,所以确定20 mg∶10 mg用作药物释放研究的浓度.
        Fe_3O_4(MNPs) was prepared by chemical co-precipitation method. Fe_3O_4(MNPs) was coated with inorganic material silica, followed by amination, and Fe_3O_4@SiO_2 and Fe_3O_4@SiO_2-NH_2 were obtained.PEGylation of Fe_3O_4@SiO_2-NH_2 and fluocin progesterone acetate(FGA) resulted in Fe_3O_4@SiO_2-NH_2-PEG and PEG-FGA products, respectively. In this experiment, the loading studies of Fe_3O_4@SiO_2-NH_2-PEG and PEG-FGA were carried out at a ratio of 20 mg:20 mg, 20 mg:10 mg respectively. Finally, the absorbance of the loaded and released samples was determined by UV-visible spectrophotometry. Therefore,the concentration of the released samples was calculated by the standard curve of FGA. The results showed that during the releasing process, the absorbance of the sample(20 mg:10 mg) at 20 d was better than that of the sample(20 mg:20 mg) at 4 d, so the concentration of 20 mg:10 mg was determined to be sufficient for the release.
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