Effects of water-soluble component content on cephalexin release from bioactive bone cement consisting of bis-GMA/TEGDMA resin and bioactive glass ceramics

被引:0
|
作者
Otsuka, M [1 ]
Sawada, M
Matsuda, Y
Nakamura, T
Kokubo, T
机构
[1] Kobe Pharmaceut Univ, Dept Pharmaceut Technol, Kobe, Hyogo 658, Japan
[2] Kyoto Univ, Fac Med, Dept Orthopaed Surg, Sakyo Ku, Kyoto 606, Japan
[3] Kyoto Univ, Fac Engn, Div Mat Chem, Sakyo Ku, Kyoto, Japan
关键词
D O I
10.1023/A:1008848328724
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The effect of the amount of a water-soluble, lactose, on cephalexin (CEX) release from bioactive bone cement consisting of bisphenol-alpha-glycidyl methacrylate (bis-GMA), triethylene-glycol dimethacrylate (TEGDMA) resin and apatite- and wollastonite-containing glass-ceramic (A-W GC) powder was investigated. A-W GC powder containing 5% CEX and lactose powders hardened within 5 min after mixing with bis-GMA/TEGDMA resin, and furthermore its compressive strength was expected to be higher than that of polymethylmethacrylate cement. In vitro CEX release from bioactive bone cement pellets in a simulated body fluid at pH 7.25 and 37 degrees C continued for more than 2 wk. The drug-release rate increased with increasing amount of lactose powder in the mixture. CEX release profiles followed the Higuchi equation in the initial stage, but not in later stages. As hydroxyapatite was precipitated out on the cement surface, the CEX release rate decreased. The micropore distribution of the cements measured by mercury porosimetry also supported the variation in drug release due to cement porosity being mainly a result of the dissolution of lactose in the cements. These results suggest that the rate of CEX release from bioactive bone cement could be controlled by varying the amount of lactose in the cement system. (C) 1999 Kluwer Academic Publishers.
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页码:59 / 64
页数:6
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