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用于硬组织再生的 3D 磷酸镁支架制备和生物活性物质加载的同步过程。

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

机构信息

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.

出版信息

Mater Sci Eng C Mater Biol Appl. 2014 Mar 1;36:252-60. doi: 10.1016/j.msec.2013.12.007. Epub 2013 Dec 14.

Abstract

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.

摘要

开发了一种新颖的室温工艺,通过糊剂挤出沉积(PED)系统和水泥化学的结合,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 PED 系统制造 3D 多孔支架生坯,在不硬化的情况下控制形态和孔结构。第二步是胶结,通过将支架生坯浸入粘合剂溶液中硬化来进行,而不是在陶瓷支架制造中进行典型的烧结过程。将制造过程和水泥反应分开对于确保有足够的时间在均匀挤出条件下制造各种尺寸和结构的 3D 支架非常重要。由于整个过程都是在室温下进行的,因此生物活性分子在加热时容易变性,可以在该过程中应用于支架。溶菌酶被选为模型生物活性物质来证明该过程的效率;它直接混入 MgP 粉末中,在支架中实现均匀分布。用于 PED 系统的挤出糊剂是使用 MgP-溶菌酶混合粉末作为起始材料制备的。也就是说,3D 支架的制造和支架的功能化可以同时进行。与典型的烧结工艺相比,该工艺显著提高了载药效率和释放性能,在典型的烧结工艺中,药物通常是通过热处理后的吸附来加载的。本研究中开发的 MgP 支架在硬组织再生的支架条件方面非常理想,包括三维相互连接的孔结构、良好的机械性能、生物降解性、良好的细胞亲和性和体外生物相容性;因此,它在生物材料领域具有优异的应用潜力。

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