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Development of a thermosensitive HAMA-containing bio-ink for the fabrication of composite cartilage repair constructs

机译:用于制备复合软骨修复构建体的含热敏性Hama的生物墨水的开发

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Fine-tuning of bio-ink composition and material processing parameters is crucial for the development of biomechanically relevant cartilage constructs. This study aims to design and develop cartilage constructs with tunable internal architectures and relevant mechanical properties. More specifically, the potential of methacrylated hyaluronic acid (HAMA) added to thermosensitive hydrogels composed of methacrylated poly[N-(2-hydroxypropyl) methacrylamide mono/dilactate] (pHPMAlac)/polyethylene glycol (PEG) triblock copolymers, to optimize cartilage-like tissue formation by embedded chondrocytes, and enhance printability was explored. Additionally, co-printing with polycaprolactone (PCL) was performed for mechanical reinforcement. Chondrocyte-laden hydrogels composed of pHPMA-lac-PEG and different concentrations of HAMA(0%-1% w/w) were cultured for 28 d in vitro and subsequently evaluated for the presence of cartilage-like matrix. Young's moduli were determined for hydrogels with the different HAMA concentrations. Additionally, hydrogel/PCL constructs with different internal architectures were co-printed and analyzed for their mechanical properties. The results of this study demonstrated a dose-dependent effect of HAMA concentration on cartilage matrix synthesis by chondrocytes. Glycosaminoglycan (GAG) and collagen type II content increased with intermediate HAMA concentrations (0.25%-0.5%) compared to HAMA-free controls, while a relatively highHAMAconcentration (1%) resulted in increased fibrocartilage formation. Young's moduli of generated hydrogel constructs ranged from 14 to 31 kPa and increased with increasing HAMA concentration. The pHPMA-lac-PEG hydrogels with 0.5% HAMA were found to be optimal for cartilage-like tissue formation. Therefore, this hydrogel system was co-printed with PCL to generate porous or solid constructs with different mesh sizes. Young's moduli of these composite constructs were in the range of native cartilage (3.5-4.6 MPa). Interestingly, the co-printing procedure influenced the mechanical properties of the final constructs. These findings are relevant for future bio-ink development, as they demonstrate the importance of selecting proper HAMA concentrations, as well as appropriate print settings and construct designs for optimal cartilage matrix deposition and final mechanical properties of constructs, respectively.
机译:生物油墨组成和材料加工参数的微调对于生物力学相关软骨构建体的开发至关重要。本研究旨在设计和开发具有可调谐内部架构和相关机械性能的软骨构建体。更具体地,将甲基丙烯酸透明质酸(HAMA)的潜力添加到由甲基丙烯酸酯化的聚[N-(2-羟丙基)甲基丙烯酰胺单/替代](PHPMALAC)/聚乙二醇(PEG)三嵌段共聚物组成的热敏水凝胶中,以优化软骨状嵌入软骨细胞组织形成,并探讨了增强可印刷性。另外,对机械加固进行了用聚己内酯(PCL)的共印。在体外培养由PHPMA-LAC-PEG和不同浓度的HAMA(0%-1%w / w)组成的软骨细胞 - 载花液(0%-1%w / w),随后评估软骨状基质的存在。杨氏的Moduli针对具有不同Hama浓度的水凝胶。另外,具有不同内部架构的水凝胶/ PCL构建体被共同印刷和分析它们的机械性能。该研究的结果表明了Hama浓度对软骨细胞包裹物质合成的剂量依赖性作用。与HAMA的对照相比,糖胺酰胺(GAG)和胶原II型含量增加(0.25%-0.5%),而相对较高的群体浓度(1%)导致纤维覆身形成增加。生成的水凝胶构建体的杨氏调节范围为14至31kPa,随着HAMA浓度的增加而增加。发现PHPMA-LAC-PEG水凝胶与0.5%HAMA的水凝胶对软骨状组织形成是最佳的。因此,该水凝胶系统用PCL共同印刷,以产生具有不同网格尺寸的多孔或固体构建体。这些复合构建体的杨氏模胶在天然软骨(3.5-4.6MPa)的范围内。有趣的是,共印过程影响了最终构建体的机械性能。这些调查结果与未来的生物墨水开发有关,因为它们证明了选择适当的HAMA浓度的重要性以及适当的打印设置,以及构建最佳的软骨基质沉积和构建体的最终机械性能的设计。

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