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Drug-loaded porous spherical hydroxyapatite granules for bone regeneration

机译:载药的多孔球形羟基磷灰石颗粒用于骨再生

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摘要

Porous spherical hydroxyapatite (HAp) granules, which are not only can be used for bone void filler, but also drug delivery systems, were prepared using a liquid nitrogen method. Various pore and channel structures of spherical granules were obtained by adjusting the ratio of water to HAp powder and the amount of sodium chloride (NaCl). By using the water to powder ratio at 2.0 ml/g and the amount of NaCl at 15 wt% by powder, the spherical granules have optimal pore volume, micro-channel structure and strength to handle as well as the ability to work as a drug delivery system. When the NaCl content was 15 wt%, the micro-channel structure was changed, but the pore volume was maintained. For the drug release test, dexamathasone (Dex) was loaded as a model drug on the prepared HAp granules by the immersion method, and the drug release behavior was curved by a UV/ vis spectrophotometer. As a result, different drug release behavior was observed according to micro-channel structural differences. Therefore, it was concluded that the NAC1 could be applied as the pore and micro-channel structure control agent. Porous spherical HAp granules, which were fabricated by a liquid nitrogen method, show potential as bone void filler with the ability of controlled drug release.
机译:使用液氮法制备了球形球形羟磷灰石(HAp)颗粒,不仅可以用作骨空隙填充剂,而且还可以用于药物输送系统。通过调节水与HAp粉末的比例以及氯化钠(NaCl)的量,可以获得球形颗粒的各种孔和通道结构。通过使用水与粉末的比例为2.0 ml / g,NaCl的含量为粉末的15 wt%,球形颗粒具有最佳的孔体积,微通道结构和处理强度,并具有作为药物起作用的能力输送系统。当NaCl含量为15wt%时,微通道结构改变,但是孔体积得以保持。对于药物释放测试,通过浸没法将地塞米松(Dex)作为模型药物装载在制备的HAp颗粒上,并且通过UV / vis分光光度计使药物释放行为弯曲。结果,根据微通道结构差异观察到不同的药物释放行为。因此,可以得出结论,NAC1可以用作孔和微通道结构控制剂。通过液氮法制备的球形球形HAp颗粒具有作为骨空隙填充剂并具有受控药物释放能力的潜力。

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  • 来源
    《Journal of materials science》 |2011年第2期|p.349-355|共7页
  • 作者单位

    Department and Research Institute of Dental Biomaterials and Bioengineering, Yonsei University College of Dentistry, Seoul 120-752, Korea;

    University of Texas at San Antonio, San Antonio, TX, USA;

    Department and Research Institute of Dental Biomaterials and Bioengineering, Yonsei University College of Dentistry, Seoul 120-752, Korea;

    Department Display and Chemical Engineering,Kyungil University, Gyeongbuk, Korea;

    University of Texas at San Antonio, San Antonio, TX, USA;

    Department and Research Institute of Dental Biomaterials and Bioengineering, Yonsei University College of Dentistry, Seoul 120-752, Korea;

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