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In Vitro Chondrocyte Culture Using Hydrophilized PLLA Scaffold in Bioreactor System

机译:在生物反应器系统中使用亲水化PLLA支架的体外软骨细胞培养

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Nonporous PLLA film and porous PLLA scaffolds were prepared and then grafted with acrylic acid (AA) using in situ direct plasma treatment to obtain PLLA-g-PAA. Chondrocytes isolated from rabbit knee articular cartilages were cultivated in Dulbecco's modified eagle medium-F12 (DMEM-F12) containing 10% fetal bovine serum (FBS) and 1% antibiotics and passaged twice before cell seeding. Once seeded on either PLLA films or scaffolds, they were placed in a bioreactor system and an intermittent hydrodynamic pressure (IHP) was applied in 3 bars, while turned on for 2 min and off for 28 min during 15-day culture. AA grafting to PLLA surface was confirmed from various surface analyses. From WST-1 assay, chondrocyte proliferation was significantly improved with dynamic IHP for PLLA and PLLA-g-PAA scaffolds as compared to static culture. This study indicates that IHP may have significant influence on chondrocytes behavior in 3D culture environment.
机译:使用原位直接等离子体处理制备无孔PLLA薄膜和多孔PLLA支架,然后用丙烯酸(AA)接枝以获得PLLA-G-PAA。从兔膝关节短关节软骨中分离的软骨细胞在Dulbecco的改性Eagle培养基-F12(DMEM-F12)中培养含有10%胎牛血清(FBS)和1%抗生素并在细胞播种前传代两次。一旦播种在PLLA薄膜或支架上,将它们置于生物反应器系统中,并且在3巴中施加间歇式流体动力学(IHP),同时在15天培养期间接通2分钟并关闭28分钟。从各种表面分析中证实了对PLLA表面的AA接枝。根据WST-1测定,与静培养相比,PLLA和PLLA-G-PAA支架的动态IHP显着改善了软骨细胞增殖。本研究表明,IHP可能对3D培养环境中的软骨细胞行为产生重大影响。

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