Physico-biological evaluation of 3D printed dECM/TOCN/alginate hydrogel based scaffolds for cartilage tissue regeneration

被引:18
|
作者
Shanto, Prayas Chakma [1 ]
Park, Seongsu [1 ]
Park, Myeongki [1 ]
Lee, Byong-Taek [1 ,2 ]
机构
[1] Soonchunhyang Univ, Coll Med, Dept Regenerat Med, Cheonan 31151, South Korea
[2] Soonchunhyang Univ, Inst Tissue Regenerat, Cheonan 31151, South Korea
来源
BIOMATERIALS ADVANCES | 2023年 / 145卷
基金
新加坡国家研究基金会;
关键词
3D printing; Decellularized extracellular matrix; Oxidized cellulose nanofiber; Tissue engineering; Cartilage regeneration; EXTRACELLULAR-MATRIX; CHONDROGENIC DIFFERENTIATION; COMPOSITE HYDROGEL; HYBRID SCAFFOLD; BONE-MATRIX; CELLULOSE; CHONDROCYTES; ALGINATE; GROWTH; CELLS;
D O I
10.1016/j.bioadv.2022.213239
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cartilage damage is the leading cause of osteoarthritis (OA), especially in an aging society. Mimicking the native cartilage microenvironment for chondrogenic differentiation along with constructing a stable and controlled architectural scaffold is considerably challenging. In this study, three-dimensional (3D) printed scaffolds using tempo-oxidized cellulose nanofiber (TOCN), decellularized extracellular matrix (dECM), and sodium alginate (SA) were fabricated for cartilage tissue regeneration. We prepared three groups (dECM80, dECM50, dECM20) of 3D printable hydrogels with different ratios of TOCN and dECM where SA concentration remained the same. Two-step crosslinking was performed with CaCl2 solution to achieve the highly stable 3D printed scaffolds. Finally, the fundamental physical characterizations showed that increasing the ratio of TOCN with dECM significantly improved the viscoelastic behaviour, stability, mechanical properties, and printability of the scaffolds. Based on the results, the 3D printed dECM50 scaffolds with controlled and identical pore sizes increased the whole-layer integrity and nutrient supply in each layer of the scaffold. Furthermore, evaluation of in vitro and in vivo biocompatibility of the scaffolds with rBMSCs indicated that dECM50 scaffolds provided a suitable microenvironment for cell proliferation and promoted chondrogenesis by remarkably expressing the cartilagespecific markers. This study demonstrates that 3D printed dECM50 scaffolds provide a favourable and promising microenvironment for cartilage tissue regeneration.
引用
收藏
页数:13
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