高等学校化学学报

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介孔分子筛孔道结构对药物巯甲丙脯酸释放性能的影响

曲凤玉1, 崔凌飞1, 黄世英2, 朱广山2   

    1. 哈尔滨师范大学化学系, 哈尔滨 150080;
    2. 吉林大学无机合成与制备化学国家重点实验室, 长春 130023
  • 收稿日期:2006-10-20 修回日期:1900-01-01 出版日期:2007-08-10 发布日期:2007-08-10
  • 通讯作者: 朱广山

Effect of Mesoporous Silica Pore Structure on the Release Profiles of Captopril Drug

QU Feng-Yu1*, CUI Ling-Fei1, HUANG Shi-Ying2, ZHU Guang-Shan2*   

    1. Department of Chemistry, Harbin Normal University, Harbin 150080, China;
    2. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, China
  • Received:2006-10-20 Revised:1900-01-01 Online:2007-08-10 Published:2007-08-10
  • Contact: ZHU Guang-Shan

摘要: 以巯甲丙脯酸为药物模型, 研究了不同孔道结构的介孔分子筛载体的药物释放性能.

关键词: 介孔分子筛, 孔道结构, 巯甲丙脯酸, 释放性能

Abstract: A series of mesoporous silica with variable pore structures were prepared. The influence of mesoporous structure on drug release profiles was studied. It is found that mesoporous pore structure has a great effect on the drug release rate. The cubic pore structure MCM-48 has a faster drug release rate than that of MCM-41 system; while SBA-16 with “cage-like” pore structure system has the lowest drug release rate.

Key words: Mesoporous silica, Pore structure, Captopril, Release property

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