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Amino-functionalized mesoporous bioactive glass for drug delivery

机译:用于药物递送的氨基官能化介孔生物活性玻璃

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An amino-functionalized mesoporous bioactive glass (N-MBG) with a high drug loading capacity and longer drug release time was successfully prepared by using 3-aminopropyltriethoxysilane (APTES) in a short-time chemical reaction. The drug release performance of an. MBG. and the. N-MBG were studied by loading gentamicin sulfate (GS) in a simulated body fluid solution. The results. showed that the surface area of the. N-MBG increases to 355.01 m(2) g(-1) after amination at 80 degrees C for 1 h compared with that of the MBG(288.07 m(2) g(-1)). Meanwhile, the surface zeta-potential of the N-MBG charges from the original negative charge (-10.06mV) to the positive charge (+5.30mV). Furthermore, the GS loading rate of the. N-MBG is up to 62.92 +/- 2.02%, higher than that of the MBG (48.90 +/- 1.71%). In addition, the. N-MBG has a longer drug release period. and the seven-day accumulative release from the. N-MBG reached. only 45.9 +/- 1.8%, significantly lower than that of the MBG, 60.7 +/- 2.3%. In vitro bioactivity tests suggested that the. N-MBG exhibited good. biological activity. In conclusion, the N-MBG with a higher loading capacity and longer drug release time can serve as a promising candidate as a. drug carrier.
机译:通过在短时间化学反应中使用3-氨基丙基三乙氧基硅烷(Aptes)成功制备具有高药物负载能力和较长药物释放时间的氨基官能化的介孔生物活性玻璃(N-MBG)。药物释放性能的。 MBG。和。通过在模拟体液溶液中加载庆大霉素(GS)来研究N-MBG。结果。表明,表面积。与MBG的80℃以80℃搅拌后,N-MBG增加到355.01m(2 )g(-1),与MBG(288.07m(2)g(-1))搅拌1小时。同时,从原始负电荷(-10.06mV)到正电荷(+ 5.30mV)的N-MBG电荷的表面Zeta电位。此外,GS加载率。 N-MBG高达62.92 +/- 2.02%,高于MBG(48.90 +/- 1.71%)。除此之外。 N-MBG具有更长的药物释放期。和七天的累计释放。 n-mbg达到了。只有45.9 +/- 1.8%,明显低于MBG,60.7 +/- 2.3%。体外生物活性试验表明。 n-mbg展出了良好的。生物活性。总之,具有较高负载能力和更长的药物释放时间的N-MBG可以作为一个有希望的候选者。药物载体。

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