Golebiowska Aleksandra A, Tan Mingyang, Ma Anson Wk, Nukavarapu Syam P
Department of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, United States of America.
Department of Chemical and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269, United States of America.
Biomed Mater. 2025 Jan 13;20(2). doi: 10.1088/1748-605X/ada59d.
Articular cartilage and osteochondral defect repair and regeneration presents significant challenges to the field of tissue engineering (TE). TE and regenerative medicine strategies utilizing natural and synthetic-based engineered scaffolds have shown potential for repair, however, they face limitations in replicating the intricate native microenvironment and structure to achieve optimal regenerative capacity and functional recovery. Herein, we report the development of a cartilage extracellular matrix (ECM) as a printable biomaterial for tissue regeneration. The biomaterial was prepared through decellularization and solubilization of articular cartilage. The effects of two different viscosity modifiers, xanthan gum and Laponite®, and the introduction of a secondary photo-crosslinkable component on the rheological behavior and stability were studied. dcECM-Laponite® bioink formulations demonstrated storage modulus (G') ranging from 750 to 4000 Pa, which is three orders of magnitude higher than that of the dcECM-XG bioink formulations. The rheological evaluation of the bioinks demonstrated the tunability of the bioinks in terms of their viscosity and degree of shear thinning, allowing the formulations to be readily extruded during 3D printing. Also, a spreadable ink composition was identified to form a uniform cartilage layer post-printing. The choice of viscosity modifier along with UV cross-linking warrants shape fidelity of the structure post-printing, as well as improvements in the storage and loss moduli. The modified ECM-based bioink also significantly improved the stability and allowed for prolonged and sustained release of loaded growth factors through the addition of Laponite®. The ECM-based bioink supported human bone-marrow derived stromal cell and chondrocyte viability and increased chondrogenic differentiation. By forming decellularized cartilage ECM biomaterials in a printable and stable bioink form, we develop a 'Cartilage Ink' that can support cartilaginous tissue formation by closely resembling the native cartilage ECM in structure and function.
关节软骨和骨软骨缺损的修复与再生给组织工程领域带来了重大挑战。利用天然和合成工程支架的组织工程和再生医学策略已显示出修复潜力,然而,它们在复制复杂的天然微环境和结构以实现最佳再生能力和功能恢复方面面临局限性。在此,我们报告了一种软骨细胞外基质(ECM)作为用于组织再生的可打印生物材料的开发。该生物材料通过对关节软骨进行脱细胞和溶解制备而成。研究了两种不同的粘度调节剂黄原胶和锂蒙脱石以及引入二次光交联组分对流变行为和稳定性的影响。dcECM - 锂蒙脱石生物墨水配方的储能模量(G')范围为750至4000 Pa,比dcECM - XG生物墨水配方高三个数量级。生物墨水的流变学评估表明,生物墨水在粘度和剪切变稀程度方面具有可调性,使得配方在3D打印过程中易于挤出。此外,还确定了一种可涂抹的墨水组合物,以便在打印后形成均匀的软骨层。粘度调节剂的选择以及紫外线交联保证了打印后结构的形状保真度,以及储能模量和损耗模量的改善。基于改性ECM的生物墨水还通过添加锂蒙脱石显著提高了稳定性,并允许负载的生长因子延长和持续释放。基于ECM的生物墨水支持人骨髓来源的基质细胞和软骨细胞的活力,并增加软骨形成分化。通过以可打印和稳定的生物墨水形式形成脱细胞软骨ECM生物材料,我们开发了一种“软骨墨水”,它可以通过在结构和功能上与天然软骨ECM非常相似来支持软骨组织的形成。