Thickett Stuart C, Hamilton Ella, Yogeswaran Gokulan, Zetterlund Per B, Farrugia Brooke L, Lord Megan S
School of Natural Sciences (Chemistry), University of Tasmania, Hobart, TAS 7001, Australia.
Graduate School of Biomedical Engineering, UNSW Sydney, Sydney, NSW 2052, Australia.
J Funct Biomater. 2019 Jul 30;10(3):33. doi: 10.3390/jfb10030033.
Poly(d,l-lactide-co-glycolide) (PLGA) has been extensively explored for bone regeneration applications; however, its clinical use is limited by low osteointegration. Therefore, approaches that incorporate osteoconductive molecules are of great interest. Graphene oxide (GO) is gaining popularity for biomedical applications due to its ability to bind biological molecules and present them for enhanced bioactivity. This study reports the preparation of PLGA microparticles via Pickering emulsification using GO as the sole surfactant, which resulted in hybrid microparticles in the size range of 1.1 to 2.4 µm based on the ratio of GO to PLGA in the reaction. Furthermore, this study demonstrated that the hybrid GO-PLGA microparticles were not cytotoxic to either primary human fetal cartilage rudiment cells or the human osteoblast-like cell line, Saos-2. Additionally, the GO-PLGA microparticles promoted the osteogenic differentiation of the human fetal cartilage rudiment cells in the absence of exogenous growth factors to a greater extent than PLGA alone. These findings demonstrate that GO-PLGA microparticles are cytocompatible, osteoinductive and have potential as substrates for bone tissue engineering.
聚(d,l-丙交酯-共-乙交酯)(PLGA)已被广泛用于骨再生应用研究;然而,其临床应用受到骨整合能力低的限制。因此,结合骨传导分子的方法备受关注。氧化石墨烯(GO)因其能够结合生物分子并增强其生物活性而在生物医学应用中越来越受欢迎。本研究报道了以GO作为唯一表面活性剂,通过Pickering乳化法制备PLGA微粒,根据反应中GO与PLGA的比例,得到了尺寸范围为1.1至2.4μm的混合微粒。此外,本研究表明,混合的GO-PLGA微粒对原代人胎儿软骨雏形细胞或人成骨样细胞系Saos-2均无细胞毒性。另外,在没有外源性生长因子的情况下,GO-PLGA微粒比单独的PLGA更能促进人胎儿软骨雏形细胞的成骨分化。这些发现表明,GO-PLGA微粒具有细胞相容性、骨诱导性,并且有潜力作为骨组织工程的基质。