Mouser V H M, Abbadessa A, Levato R, Hennink W E, Vermonden T, Gawlitta D, Malda J
Department of Orthopaedics, University Medical Center Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands.
Biofabrication. 2017 Mar 23;9(1):015026. doi: 10.1088/1758-5090/aa6265.
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] (pHPMA-lac)/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 high HAMA concentration (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.
生物墨水成分和材料加工参数的微调对于开发具有生物力学相关性的软骨构建体至关重要。本研究旨在设计和开发具有可调内部结构和相关力学性能的软骨构建体。更具体地说,探索了将甲基丙烯酸化透明质酸(HAMA)添加到由甲基丙烯酸化聚[N-(2-羟丙基)甲基丙烯酰胺单/双乳酸酯](pHPMA-lac)/聚乙二醇(PEG)三嵌段共聚物组成的热敏水凝胶中,以优化嵌入软骨细胞的类软骨组织形成并提高可打印性的潜力。此外,还进行了与聚己内酯(PCL)的共打印以增强机械性能。由pHPMA-lac-PEG和不同浓度的HAMA(0%-1% w/w)组成的负载软骨细胞的水凝胶在体外培养28天,随后评估类软骨基质的存在情况。测定了不同HAMA浓度水凝胶的杨氏模量。此外,对具有不同内部结构的水凝胶/PCL构建体进行了共打印,并分析了它们的力学性能。本研究结果表明HAMA浓度对软骨细胞合成软骨基质具有剂量依赖性效应。与无HAMA的对照组相比,中等HAMA浓度(0.25%-0.5%)时糖胺聚糖(GAG)和II型胶原蛋白含量增加,而相对较高的HAMA浓度(1%)导致纤维软骨形成增加。生成的水凝胶构建体的杨氏模量范围为14至31 kPa,并随HAMA浓度的增加而增加。发现含0.5% HAMA的pHPMA-lac-PEG水凝胶最适合类软骨组织形成。因此,将该水凝胶系统与PCL共打印以生成具有不同网孔尺寸的多孔或实心构建体。这些复合构建体的杨氏模量在天然软骨范围内(3.5-4.6 MPa)。有趣的是,共打印过程影响了最终构建体的力学性能。这些发现与未来生物墨水的开发相关,因为它们分别证明了选择合适的HAMA浓度以及适当的打印设置和构建体设计对于优化软骨基质沉积和构建体最终力学性能的重要性。