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Mesoporous bioactive glass nanoparticles doped with magnesium: drug delivery and acellular in vitro bioactivity

机译:掺杂镁的中孔生物活性玻璃纳米颗粒:药物递送和无细胞体外生物活性

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The effects of the magnesium doping of binary glass (Si–Ca) on particle texture, on the biomineralization process in simulated body fluid (SBF) as well as on drug loading and release were examined. For this purpose, magnesium-doped binary bioglass nanoparticles (85SiO _(2) –(15 ? x )CaO– x MgO, with x = 1, 3, 5 and 10 mol%) were prepared by a base catalysed sol–gel method. N _(2) adsorption isotherm analysis showed an enhancement in specific surface area as the Mg molar fraction increased. In addition, the FTIR spectra of the samples after soaking in SBF for various periods of time confirmed the presence of new chemical bonds related to the apatite phase, as was also confirmed by SEM observations. XRD patterns of the samples after soaking revealed that the crystallization to form a more stable apatite-like phase was hindered with increasing magnesium content in the glass composition. Furthermore, it was proved that the kinetics of drug release improved with increasing magnesium content. The porosity and the specific surface area were found to be responsible for this improvement.
机译:研究了二元玻璃(Si-Ca)的镁掺杂对颗粒质地,模拟体液(SBF)中生物矿化过程以及药物装载和释放的影响。为此,通过碱催化溶胶-凝胶法制备了镁掺杂的二元生物玻璃纳米粒子(85SiO _(2)–(15 x)CaO– x MgO,x = 1、3、5和10 mol%)。 。 N _(2)吸附等温线分析表明,随着Mg摩尔分数的增加,比表面积增加。另外,样品在SBF中浸泡了不同时间后的FTIR光谱证实了与磷灰石相有关的新化学键的存在,这也通过SEM观察得到了证实。浸泡后样品的XRD图谱表明,随着玻璃组合物中镁含量的增加,形成更稳定的磷灰石样相的结晶受到阻碍。此外,已经证明,随着镁含量的增加,药物释放动力学得以改善。发现孔隙率和比表面积是造成这种改善的原因。

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