用于骨软骨移植发育的脱细胞软骨组织生物链接配方。

Aleksandra A Golebiowska, Mingyang Tan, Anson Wk Ma, Syam P Nukavarapu
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引用次数: 0

摘要

关节软骨和骨软骨缺损的修复和再生是组织工程(TE)领域面临的重大挑战。利用天然和基于合成的工程支架的TE和再生医学策略显示出修复的潜力,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,我们报告了软骨细胞外基质(ECM)作为组织再生的可打印生物材料的发展。该生物材料是通过关节软骨的脱细胞和增溶制备的。研究了黄原胶和拉脱石两种不同的粘弹性改性剂,以及引入二次光交联组分对其流变性能和稳定性的影响。生物墨水的流变学评估证明了生物墨水在粘度和剪切变薄程度方面的可调性,使得配方在3D打印过程中很容易被挤出。dcECM-Laponite®生物墨水配方的流变特性G′范围为750至4000 Pa,比dcECM-XG生物墨水配方高出三个数量级。此外,交联后G′在2400 ~ 5700Pa范围内进一步增加。本文确定了一种可涂抹的油墨组合物,用于在印刷后形成均匀的软骨层。粘度调节剂的选择以及UV交联保证了打印后结构的形状保真度,以及存储和损失模量的改进。改性的基于ecm的生物链接也显著提高了稳定性,并允许通过添加Laponite®延长和持续释放负载的生长因子。在体外,基于ecm的生物链接支持人骨髓基质细胞和软骨细胞的活力,并增加软骨细胞分化。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细胞外基质非常相似来支持软骨组织的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decellularized cartilage tissue bioink formulation for osteochondral graft development.

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 differentiationin vitro. 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.

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