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.
引文
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