首页> 外文期刊>Materials science & engineering >A simultaneous process of 3D magnesium phosphate scaffold fabrication and bioactive substance loading for hard tissue regeneration
【24h】

A simultaneous process of 3D magnesium phosphate scaffold fabrication and bioactive substance loading for hard tissue regeneration

机译:3D磷酸镁支架制造与生物活性物质加载的同时过程,用于硬组织再生

获取原文
获取原文并翻译 | 示例
           

摘要

A novel room temperature process was developed to produce a 3D porous magnesium phosphate (MgP) scaffold with high drug load/release efficiency for use in hard tissue regeneration through a combination of a paste extruding deposition (PED) system and cement chemistry. MgP scaffolds were prepared using a two-step process. The first step was fabrication of the 3D porous scaffold green body to control both the morphology and pore structure using a PED system without hardening. The second step was cementation, which was carried out by immersing the scaffold green body in the binder solution for hardening instead of the typical sintering process in ceramic scaffold fabrication. Separation of the manufacturing process and cement reaction was important to secure enough time to fabricate a 3D scaffold with various sizes and architectures under homogeneous extruding conditions. Because the whole process is carried out at room temperature, the bioactive molecules, which are easily denatured by heat, may apply to scaffolds during the process. Lysozyme was selected as a model bioactive substance to demonstrate the efficiency of this process; this was directly mixed into MgP powder to introduce homogeneous distribution in the scaffold. The extruding paste for the PED system was prepared using the MgP-lysozyme blended powder as starting materials. That is, both 3D scaffold fabrication and functionalization of the scaffold with bioactive substances could be carried out simultaneously. This process significantly enhanced both drug loading efficiency and release performance compared to the typical sintering process, where the drug is generally loaded by adsorption after heat treatment The MgP scaffold developed in this study satisfied the required conditions for scaffolding in hard tissue regeneration in an ideal manner, including 3 dimensionally well-interconnected pore structures, favorable mechanical properties, biodegradability, good cell affinity and in vitro biocompatibility; thus, it has excellent potential for application in the field of biomaterials.
机译:通过将糊料挤出沉积(PED)系统和水泥化学方法相结合,开发了一种新颖的室温工艺来生产具有高载药量/释放效率的3D多孔磷酸镁(MgP)支架,用于硬组织再生。使用两步法制备MgP支架。第一步是使用不硬化的PED系统制造3D多孔支架生坯,以控制形态和孔结构。第二步是胶结,这是通过将支架生坯浸入粘合剂溶液中进行硬化来代替陶瓷支架制造中的典型烧结过程来进行的。制造过程和水泥反应的分离对于确保有足够的时间在均质挤出条件下制造具有各种尺寸和结构的3D支架至关重要。因为整个过程都是在室温下进行的,所以容易被热变性的生物活性分子可能会在过程中施加到支架上。选择溶菌酶作为模型生物活性物质,以证明该过程的效率。将其直接混入MgP粉末中,以在支架中引入均匀分布。以MgP-溶菌酶混合粉为原料,制备用于PED系统的挤出糊剂。即,可以同时进行3D支架制造和具有生物活性物质的支架功能化。与典型的烧结过程相比,该过程显着提高了药物装载效率和释放性能,在典型的烧结过程中,通常通过热处理后的吸附来装载药物。本研究开发的MgP支架以理想的方式满足了硬组织再生中支架的必要条件。包括3个尺寸良好的相互连通的孔结构,良好的机械性能,可生物降解性,良好的细胞亲和力和体外生物相容性;因此,它在生物材料领域具有极好的应用潜力。

著录项

  • 来源
    《Materials science & engineering》 |2014年第3期|252-260|共9页
  • 作者单位

    Powder & Ceramics Division, Korea Institute of Materials Science (KIMS), 797 Changwondaero, Changwon 641-831, Republic of Korea;

    Powder & Ceramics Division, Korea Institute of Materials Science (KIMS), 797 Changwondaero, Changwon 641-831, Republic of Korea,Biomaterials Department, National Research Centre (NRC), 33 El-Bohooth St, Dokki 12622, Egypt;

    School of Dentistry, Kyungpook National University, Daegu 700-422, Republic of Korea;

    School of Dentistry, Kyungpook National University, Daegu 700-422, Republic of Korea;

    Powder & Ceramics Division, Korea Institute of Materials Science (KIMS), 797 Changwondaero, Changwon 641-831, Republic of Korea;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Magnesium phosphate; Room temperature fabrication; Paste extruding deposition; Bone scaffold; Direct drug loading;

    机译:磷酸镁;室温制作;糊状挤出沉积;骨支架直接上药;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号