School of Engineering, Institute for Bioengineering, University of Edinburgh, Edinburgh, United Kingdom.
Biomed Mater. 2018 Jun 27;13(5):051001. doi: 10.1088/1748-605X/aac91f.
Osteoarthritis is the leading cause of pain and disability worldwide. Despite treatment availability, fully functional and suitable long term treatments for large cartilage defects are yet to be sought. Cartilage tissue engineering provides an alternative treatment option with the potential of cartilage regeneration. Previously, scaffolds have been enhanced through coating with collagen type I, however, equal distribution of collagen and collagen penetration throughout the scaffold have been poor. Herein, this study aims to employ thermally induced phase separation to fabricate porous hybrid polycaprolactone (PCL)/collagen type I scaffolds, with equally distributed collagen type I throughout the scaffold. PCL/collagen scaffolds were produced using polycaprolactone, varying concentrations of collagen type I and acetic acid as the solvent. Scaffolds were seeded with chondrocytes for 14 days. Scaffolds possessed an interconnected and porous structure, which altered with an increase in collagen concentration. Collagen type I antibody staining revealed the presence of equally distributed collagen within the PCL fibres. A reduction in collagen type I concentration influenced the compressive properties of the PCL/collagen type 1 scaffolds. Specifically, 0.2% wt/vol concentration of collagen presented to have compressive properties similar to that of the native cartilage at 10% strain. All scaffolds allowed cell attachment and collagen scaffolds showed a greater number of viable chondrocytes after 14 days of culture, compared to PCL control. This study demonstrated the ability of fabricating PCL/collagen type I scaffolds which exhibit easily tuneable porosity and compressive properties. Further investigation on the long term feasibility of these scaffolds is warranted.
骨关节炎是全球范围内导致疼痛和残疾的主要原因。尽管有治疗方法,但仍在寻找可完全发挥功能且适合长期治疗的大型软骨缺损的方法。软骨组织工程提供了一种替代治疗选择,具有软骨再生的潜力。以前,通过涂覆 I 型胶原蛋白来增强支架,但胶原蛋白的均匀分布和胶原蛋白在整个支架中的渗透一直很差。在此,本研究旨在通过热致相分离来制造多孔混合聚己内酯 (PCL)/I 型胶原蛋白支架,使胶原蛋白在支架中均匀分布。使用聚己内酯、不同浓度的 I 型胶原蛋白和乙酸作为溶剂来制备 PCL/胶原蛋白支架。将软骨细胞接种到支架上培养 14 天。支架具有相互连接的多孔结构,随着胶原蛋白浓度的增加而改变。I 型胶原蛋白抗体染色显示胶原蛋白均匀分布在 PCL 纤维内。胶原蛋白浓度的降低影响了 PCL/胶原蛋白 I 型支架的压缩性能。具体来说,0.2%wt/vol 浓度的胶原蛋白在 10%应变下表现出与天然软骨相似的压缩性能。所有支架都允许细胞附着,与 PCL 对照相比,胶原蛋白支架在培养 14 天后显示出更多的活软骨细胞。本研究表明能够制造具有易于调节的孔隙率和压缩性能的 PCL/胶原蛋白 I 型支架。需要进一步研究这些支架的长期可行性。