Meiho University Institutional Repository:Item 987654321/2577
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 2876/3793 (76%)
造访人次 : 3856337      在线人数 : 503
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻
    主页登入上传说明关于MUIR管理 到手机版


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.meiho.edu.tw/ir/handle/987654321/2577


    题名: Characterization and human osteoblastic proliferation- and differentiation-stimulatory effects of phosphatidylcholine liposomes-encapsulated propranolol hydrochloride
    作者: Benjamin Teong;Shyh-Ming Kuo;Chung-Hwan Chen;Yu-Kuei Chen
    贡献者: 健康暨護理學院
    日期: 2014
    上传时间: 2014-10-17T03:52:31Z (UTC)
    摘要: DMPC and DSPC liposomes were prepared via thin film hydration method followed by sonication. Propranolol solution
    was incorporated into liposomes at hydration stage. TEM images showed the sizes of DSPC and DMPC were around
    88 and 137 nm, respectively. The highest encapsulation ratio of propranolol was approximately 70% using DSPC/CHO/OCT
    liposomes, which release the drug over 60% in 24 h and reached 100% in 48 h. Both propranolol (10−8–10−6 M) and DSCP
    liposomes-encapsulated propranolol showed over 1.5-fold increases in the proliferation of human osteoblastic cells hFOB1.19
    while differentiation of the cells was approximately doubled by plain and liposomal propranolol, indicating that the stimulatory
    effects of liposomal propranolol are similar with those of propranolol on human osteoblastic hFOB1.19 cells. The phosphatidylcholine
    liposomes-encapsulated propranolol prepared in this study potentially possesses anabolic effects in vivo and is also a
    promising anti-osteoporotic agent in future.
    關聯: Bio-Medical Materials and Engineering
    显示于类别:[美容系] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    BME997 author version.pdf336KbAdobe PDF0检视/开启


    在MUIR中所有的数据项都受到原著作权保护.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈