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Nanocrystalline spherical hydroxyapatite granules for bone repair: in vitro evaluation with osteoblast-like cells and osteoclasts

机译:纳米晶球形羟基磷灰石颗粒用于骨修复:体外评估成骨细胞样细胞和破骨细胞

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摘要

Conventionally sintered hydroxyapatite-based materials for bone repair show poor resorbability due to the loss of nanocrystallinity. The present study describes a method to establish nanocrystalline hydroxyapatite granules. The material was prepared by ionotropic gelation of an alginate sol containing hydroxyapatite (HA) powder. Subsequent thermal elimination of alginate at 650 ℃ yielded non-sintered, but unexpectedly stable hydroxyapatite granules. By adding stearic acid as an organic filler to the alginate/HA suspension, the granules exhibited mac-ropores after thermal treatment. A third type of material was achieved by additional coating of the granules with silica particles. Microstructure and specific surface area of the different materials were characterized in comparison to the already established granular calcium phosphate material Cerasorb M~®. Cytocompatibility and potential for bone regeneration of the materials was evaluated by in vitro examinations with osteosarcoma cells and osteoclasts. Osteoblast-like SaOS-2 cells proliferated on all examined materials and showed the typical increase of alkaline phosphatase (ALP) activity during cultivation. Expression of bone-related genes coding for ALP, osteonectin, osteo-pontin, osteocalcin and bone sialoprotein II on the materials was proven by RT-PCR. Human monocytes were seeded onto the different granules and osteoclastogenesis was examined by activity measurement of tartrate-specific acid phosphatase (TRAP). Gene expression analysis after 23 days of cultivation revealed an increased expression of osteoclast-related genes TRAP, vitronectin receptor and cathepsin K, which was on the same level for all examined materials. These results indicate, that the nanocrystalline granular materials are of clinical interest, especially for bone regeneration.
机译:常规地,用于骨修复的烧结的基于羟基磷灰石的材料由于纳米结晶度的损失而显示出差的再吸收性。本研究描述了一种建立纳米晶羟基磷灰石颗粒的方法。该材料是通过对含有羟基磷灰石(HA)粉末的藻酸盐溶胶进行离子凝胶化而制备的。随后在650℃下热去除藻酸盐,得到未烧结但出乎意料稳定的羟基磷灰石颗粒。通过将硬脂酸作为有机填料加入藻酸盐/ HA悬浮液中,在热处理后,颗粒显示出宏孔。第三类材料是通过用二氧化硅颗粒另外涂覆颗粒而获得的。与已经建立的颗粒状磷酸钙材料Cerasorb M相比,对不同材料的微观结构和比表面积进行了表征。通过用骨肉瘤细胞和破骨细胞进行体外检查来评估材料的细胞相容性和骨再生潜力。成骨细胞样SaOS-2细胞在所有检查的材料上均增殖,并在培养过程中显示出碱性磷酸酶(ALP)活性的典型增加。通过RT-PCR证实了编码ALP,骨连接蛋白,骨桥蛋白,骨钙蛋白和骨唾液蛋白II的骨相关基因的表达。将人单核细胞接种到不同的颗粒上,并通过酒石酸特异性酸性磷酸酶(TRAP)的活性测量来检测破骨细胞的形成。培养23天后的基因表达分析表明,破骨细胞相关基因TRAP,玻连蛋白受体和组织蛋白酶K的表达增加,所有受检材料的表达水平均相同。这些结果表明,纳米晶颗粒材料具有临床意义,特别是对于骨再生。

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  • 来源
    《Journal of materials science》 |2013年第7期|1755-1766|共12页
  • 作者单位

    Centre for Translational Bone, Joint and Soft Tissue Research, Medical Faculty of Technische Universitaet Dresden and University Hospital Carl Gustav Carus, Fetscher Str. 74, 01307 Dresden, Germany;

    TU Bergakademie Freiberg, Institute of Electronic and Sensor Materials, Gustav-Zeuner-Str. 3, 09596 Freiberg, Germany;

    Centre for Translational Bone, Joint and Soft Tissue Research, Medical Faculty of Technische Universitaet Dresden and University Hospital Carl Gustav Carus, Fetscher Str. 74, 01307 Dresden, Germany;

    Centre for Translational Bone, Joint and Soft Tissue Research, Medical Faculty of Technische Universitaet Dresden and University Hospital Carl Gustav Carus, Fetscher Str. 74, 01307 Dresden, Germany;

    Centre for Translational Bone, Joint and Soft Tissue Research, Medical Faculty of Technische Universitaet Dresden and University Hospital Carl Gustav Carus, Fetscher Str. 74, 01307 Dresden, Germany;

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