Optimization of the Rheological Properties of Self-Assembled Tripeptide/Alginate/Cellulose Hydrogels for 3D Printing

自愈水凝胶 材料科学 纤维素 脚手架 组织工程 三维细胞培养 化学工程 胶粘剂 生物加工 流变学 纳米技术 化学 高分子化学 生物医学工程 复合材料 细胞 生物化学 医学 图层(电子) 工程类
作者
Alejandro Hernández-Sosa,Rosa Ana Ramírez-Jiménez,Luís Rojo,Fouzia Boulmedais,María Rosa Aguilar,Miryam Criado‐Gonzalez,Rebeca Hernández
出处
期刊:Polymers [Multidisciplinary Digital Publishing Institute]
卷期号:14 (11): 2229-2229 被引量:28
标识
DOI:10.3390/polym14112229
摘要

3D printing is an emerging and powerful technique to create shape-defined three-dimensional structures for tissue engineering applications. Herein, different alginate-cellulose formulations were optimized to be used as printable inks. Alginate (Alg) was chosen as the main component of the scaffold due to its tunable mechanical properties, rapid gelation, and non-toxicity, whereas microcrystalline cellulose (MCC) was added to the hydrogel to modulate its mechanical properties for printing. Additionally, Fmoc-FFY (Fmoc: 9-fluorenylmethoxycarbonyl; F: phenylalanine; Y: tyrosine), a self-assembled peptide that promotes cell adhesion was incorporated into the ink without modifying its rheological properties and shear-thinning behavior. Then, 3D-printed scaffolds made of Alg, 40% of MCC inks and Fmoc-FFY peptide were characterized by scanning electron microscopy and infrared spectroscopy, confirming the morphological microstructure of the hydrogel scaffolds with edged particles of MCC homogeneously distributed within the alginate matrix and the self-assembly of the peptide in a β-sheet conformation. Finally, the cytocompatibility of the scaffolds was tested in contact with the MG63 osteosarcoma cells, confirming the absence of cytotoxic components that may compromise their viability. Interestingly, MG63 cell growth was retarded in the scaffolds containing the peptide, but cells were more likely to promote adhesive interactions with the material rather than with the other cells, indicating the benefits of the peptide in promoting biological functionality to alginate-based biomaterials.

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