Department of Chemical and Biomolecular Engineering, Seoul National University of Science and Technology, Seoul 01811, Republic of Korea.
Convergence Institute of Biomedical Engineering and Biomaterials, Seoul National University of Science and Technology, Seoul 01811, Republic of Korea.
Biofabrication. 2020 Sep 15;12(4):045026. doi: 10.1088/1758-5090/aba2f7.
One of the primary challenges in extrusion-based 3D bioprinting is the ability to print self-supported multilayered constructs with biocompatible hydrogels. The bioinks should have sufficient post-printing mechanical stability for soft tissue and organ regeneration. Here, we report on the synthesis, characterization and 3D printability of hyaluronic acid (HA)-carboxymethylcellulose (CMC) hydrogels cross-linked through N-acyl-hydrazone bonding. The hydrogel's hydrolytic stability was acquired by the effects of both the prevention of the oxidation of the six-membered rings of HA, and the stabilization of acyl-hydrazone bonds. The shear-thinning and self-healing properties of the hydrogel allowed us to print different 3D constructs (lattice, cubic and tube) of up to 50 layers with superior precision and high post-printing stability without support materials or post-processing depending on their compositions (H7:C3, H5:C5 and H3:C7). Morphological analyses of different zones of the 3D-printed constructs were undertaken for verification of the interconnection of pores. Texture profile analysis (TPA) (hardness (strength), elastic recovery, etc) and cyclic compression studies of the 3D-printed constructs demonstrated exceptional elastic properties and fast recovery after 50% strain, respectively, which have been attributed to the addition of CMC into HA. A model drug quercetin was released in a sustained manner from hydrogels and 3D constructs. In vitro cytotoxicity studies confirmed the excellent cyto-compatibility of these gels. In vivo mice studies prove that these biocompatible hydrogels enhance angiogenesis. The results indicate that controlling the key properties (e.g. self-crosslinking capacity, composition) can lead to the generation of multilayered constructs from 3D-bioprintable HA-CMC hydrogels capable of being leveraged for soft tissue engineering applications.
挤出式 3D 生物打印面临的主要挑战之一是能够使用生物相容性水凝胶打印具有自我支撑的多层结构。生物墨水应该具有足够的打印后机械稳定性,以用于软组织和器官再生。在这里,我们报告了通过 N-酰腙键交联合成、表征和 3D 可打印性的透明质酸(HA)-羧甲基纤维素(CMC)水凝胶。水凝胶的水解稳定性是通过防止 HA 六元环的氧化和酰腙键的稳定的双重作用获得的。水凝胶的剪切变稀和自修复特性使我们能够打印不同的 3D 结构(格子、立方和管),最多可达 50 层,具有卓越的精度和高打印后稳定性,无需支撑材料或后处理,具体取决于其组成(H7:C3、H5:C5 和 H3:C7)。对 3D 打印结构的不同区域进行形态分析,以验证孔的连通性。不同区域的纹理轮廓分析(TPA)(硬度(强度)、弹性恢复等)和 3D 打印结构的循环压缩研究表明,其具有出色的弹性特性和在 50%应变后的快速恢复能力,这归因于 CMC 被添加到 HA 中。模型药物槲皮素从水凝胶和 3D 结构中以持续的方式释放。体外细胞毒性研究证实了这些凝胶的出色细胞相容性。体内小鼠研究证实这些生物相容性水凝胶可促进血管生成。结果表明,控制关键特性(例如自交联能力、组成)可以从 3D 可打印的 HA-CMC 水凝胶生成用于软组织工程应用的多层结构。