Fakhri Vafa, Jafari Aliakbar, Zeraatkar Ali, Rahimi Maryam, Hadian Hooriyeh, Nouranian Sasan, Kruppke Benjamin, Khonakdar Hossein Ali
Department of Polymer Engineering & Color Technology, Amirkabir University of Technology, Tehran, Iran.
Department of Chemical Engineering, Faculty of Technical and Engineering, Islamic Azad University, Central Tehran Branch, Tehran, Iran.
J Mater Chem B. 2023 Jan 4;11(2):452-470. doi: 10.1039/d2tb01628a.
As a glycerol-based polyester, poly(glycerol azelaic acid) (PGAz) has shown great potential for biomedical applications, such as tissue engineering. However, it tends to show low mechanical strength and a relatively fast biodegradation rate, limiting its capability of mimicking and supporting a broad range of hard tissues such as bone. Moreover, the typical thermal curing process of poly(glycerol--diacids) is one of their drawbacks. To overcome these limitations, glycidyl methacrylate (GMA) moieties were first grafted on the backbone of PGAz herein to achieve a UV-curable PGAz--GMA (PGAG) resin. Then polyvinylidene fluoride (PVDF), nano-hydroxyapatite, and Cloisite Na nanoclay were used to fabricate photo-crosslinked PGAG/PVDF nanocomposites with efficient properties to mimic various hard tissues. Our results demonstrated that all nanocomposites possessed a semi-crystalline structure with noticeable PVDF β-phase fraction. The scaffolds yielded Young's modulus, ultimate tensile strength, and elongation at break of 15-24 MPa, 13-15 MPa, and 50-65%, respectively that could meet the requirements for supporting cancellous bone tissue. The presence of nanofillers improved the hydrophilicity and slightly accelerated the biodegradation rate of the scaffolds. Additionally, it was illustrated that the scaffolds had no noticeable cytotoxicity, and mouse fibroblast L929 cells and osteoblast MG-63 cells attached to and proliferated on their surface desirably. Our findings indicate that the PGAG/PVDF blend and its nanocomposites could be high-potential candidates for a range of hard tissues, specifically cancellous bones.
作为一种基于甘油的聚酯,聚壬二酸甘油酯(PGAz)在生物医学应用领域,如组织工程方面展现出了巨大的潜力。然而,它往往表现出较低的机械强度和相对较快的生物降解速率,这限制了其模拟和支撑多种硬组织(如骨骼)的能力。此外,聚(甘油 - 二酸)的典型热固化过程是其缺点之一。为了克服这些限制,本文首先将甲基丙烯酸缩水甘油酯(GMA)部分接枝到PGAz的主链上,以获得可紫外光固化的PGAz - GMA(PGAG)树脂。然后使用聚偏氟乙烯(PVDF)、纳米羟基磷灰石和钠基蒙脱土制备具有有效性能的光交联PGAG/PVDF纳米复合材料,以模拟各种硬组织。我们的结果表明,所有纳米复合材料都具有半结晶结构,且PVDFβ相分数显著。这些支架的杨氏模量、极限拉伸强度和断裂伸长率分别为15 - 24 MPa、13 - 15 MPa和50 - 65%,能够满足支撑松质骨组织的要求。纳米填料的存在改善了支架的亲水性,并略微加速了其生物降解速率。此外,结果表明该支架没有明显的细胞毒性,小鼠成纤维细胞L929和骨细胞MG - 63能够很好地附着在其表面并在上面增殖。我们的研究结果表明,PGAG/PVDF共混物及其纳米复合材料可能是一系列硬组织,特别是松质骨的高潜力候选材料。