软骨发生
细胞外基质
自愈水凝胶
脚手架
阿格里坎
生物医学工程
化学
软骨
壳聚糖
细胞生长
肿胀 的
间充质干细胞
细胞
关节软骨修复
组织工程
基质(化学分析)
关节软骨
生物物理学
体外
细胞培养
去细胞化
II型胶原
细胞外
细胞迁移
材料科学
细胞生物学
生物材料
软骨细胞
作者
Vukašin Ugrinović,Đorđe Veljović,Tamara Matić,Julijana Tadić,Per Wretenberg,Mikael Ivarsson,Nenad Andjelkov
出处
期刊:Cartilage
[SAGE]
日期:2025-12-23
卷期号:: 19476035251407298-19476035251407298
标识
DOI:10.1177/19476035251407298
摘要
Objective The aim was to investigate starch-gelatin hydrogels as scaffolds for chondrogenesis and compare these with other materials currently in use regarding cell retention and growth. Methods Two variants of starch-gelatin-scaffolds and one chitosan-based scaffold were fabricated by casting and freeze-drying. The resulting materials were analyzed with respect to physicochemical and mechanical properties, cut to size, and seeded with human articular chondrocytes. Cell retention and proliferation were evaluated at 1, 14, and 42 days of culturing. Extracellular matrix production was analyzed by histo- and immunohistochemistry. Comparisons were made with that of commercially available hyaluronan- (Hyalofast ® ) and collagen-based (ChondroGide ® ) scaffolds, and synthesized chitosan hydrogels. Results The starch-gelatin materials exhibited highly porous structures stabilized by hydrogen bonding, with swelling behavior similar to native cartilage and favorable mechanical handling properties. Despite differences in initial cell retention, all materials except chitosan supported robust cell growth, reaching similar levels after 14 days. No significant changes were observed between 14 and 42 days with the exception of Hyalofast ® showing decreased cell number. Chitosan-supported cell growth was more linear over the culture period, but resulted in only half the cell number by day 42 compared with the other materials. Without cells, Hyalofast and one variant of the starch/gelatin hydrogel degraded before day 42. starch/gelatin scaffolds showed collagen I, II, and aggrecan deposition. Conclusion Starch-gelatin scaffolds displayed favorable mechanical properties, supported cell growth comparable to commercial scaffolds, and promoted deposition of cartilage-specific extracellular matrix, highlighting their chondrogenic potential
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