Biomedical Engineering Faculty, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran.
Dental Research Center, Research Institute of Dental Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Cell Physiol. 2021 Mar;236(3):2194-2204. doi: 10.1002/jcp.30006. Epub 2020 Aug 10.
In this study, we developed an injectable in situ forming hydrogel/microparticle system consisting of two drugs, melatonin and methylprednisolone, to investigate the capability of the system for chondrogenesis in vitro and in vivo. The chemical, mechanical, and rheological properties of the hydrogel/microparticle were investigated. For in vitro evaluation, the adipose-derived stem cells might be mixed with hydrogel/microparticles, then cellular viability was analyzed by acridine orange/propidium iodide and 4',6-diamidino-2-phenylindole staining and also dimethylmethylene blue assay were conducted to find the amount of proteoglycan. The real-time polymerase chain reaction for aggrecan, sex-determining region Y-Box 9, collagen I (COL1), and COL2 gene expression was performed after 14 and 21 days. For evaluation of cartilage regeneration, the samples were implanted in rabbit knees with cartilaginous experimental defects. Defects were created in both knees of three groups of rabbits. Group 1 was the control with no injection, and Groups 2 and 3 were loaded with hydrogel/cell and hydrogel/microparticle/cell; respectively. Then, after 3 and 6 months, histological evaluations of the defected sites were carried out. The amount of glycosaminoglycans after 14 and 21 days increased significantly in hydrogels/microparticles loaded with cells. The expression of marker genes was also significant in hydrogels/microparticles loaded with cells. According to histology analysis, the hydrogels/microparticles loaded with cells showed the best cartilage regeneration. Overall, our study revealed that the developed injectable hydrogel/microparticle can be used for cartilage regeneration.
在这项研究中,我们开发了一种由两种药物(褪黑素和甲泼尼龙)组成的可注射原位形成水凝胶/微球系统,以研究该系统在体外和体内的软骨生成能力。研究了水凝胶/微球的化学、机械和流变性能。为了进行体外评估,可以将脂肪来源的干细胞与水凝胶/微球混合,然后通过吖啶橙/碘化丙啶染色和二甲亚甲基蓝测定分析细胞活力,并测定蛋白聚糖的含量。通过实时聚合酶链反应分析 14 天和 21 天后聚集蛋白聚糖、性别决定区 Y 盒 9、胶原 I(COL1)和 COL2 基因的表达。为了评估软骨再生,将样品植入具有软骨实验性缺损的兔膝关节中。在三组兔子的每只膝盖上都创建了缺陷。第 1 组为对照,未注射,第 2 组和第 3 组分别加载水凝胶/细胞和水凝胶/微球/细胞。然后,在 3 个月和 6 个月后,对缺陷部位进行组织学评估。第 14 天和第 21 天,加载细胞的水凝胶/微球中糖胺聚糖的含量显著增加。加载细胞的水凝胶/微球中标记基因的表达也很显著。根据组织学分析,加载细胞的水凝胶/微球显示出最佳的软骨再生。总体而言,我们的研究表明,开发的可注射水凝胶/微球可用于软骨再生。