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Surface modification of PdlLGA microspheres with gelatine methacrylate: evaluation of adsorption, entrapment, and oxygen plasma treatment approaches

机译:用甲基丙烯酸明胶对PdlLGA微球进行表面改性:评估吸附,截留和氧等离子体处理方法

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摘要

Injectable poly (dl-lactic-co-glycolic acid) (PdlLGA) microspheres are promising candidates as biodegradable controlled release carriers for drug and cell delivery applications; however, they have limited functional groups on the surface to enable dense grafting of tissue specific biocompatible molecules. In this study we have evaluated surface adsorption, entrapment and oxygen plasma treatment as three approaches to modify the surfaces of PdlLGA microspheres with gelatine methacrylate (gel-MA) as a biocompatible and photo cross-linkable macromolecule. Time of flight secondary ion mass spectroscopy (TOF SIMS) and X-ray photoelectron spectroscopy (XPS) were used to detect and quantify gel-MA on the surfaces. Fluorescent and scanning electron microscopies (SEM) were used to image the topographical changes. Human mesenchymal stem cells (hMSCs) of immortalised cell line were cultured on the surface of gel-MA modified PdlLGA microspheres and Presto-Blue assay was used to study the effect of different surface modifications on cell proliferation. Data analysis showed that the oxygen plasma treatment approach resulted in the highest density of gel-MA deposition. This study supports oxygen plasma treatment as a facile approach to modify the surface of injectable PdlLGA microspheres with macromolecules such as gel-MA to enhance proliferation rate of injected cells and potentially enable further grafting of tissue specific molecules.
机译:可注射的聚(dl-乳酸-乙醇酸共聚物)(PdlLGA)微球有望成为可生物降解的控释载体,用于药物和细胞递送应用。然而,它们在表面上具有有限的官能团,以能够致密地移植组织特异性生物相容性分子。在这项研究中,我们评估了表面吸附,截留和氧等离子体处理作为三种方法来修饰明胶甲基丙烯酸酯(gel-MA)作为生物相容性和光可交联大分子的PdlLGA微球表面。飞行时间二次离子质谱(TOF SIMS)和X射线光电子能谱(XPS)用于检测和定量表面上的gel-MA。荧光和扫描电子显微镜(SEM)用于成像的地形变化。将永生化细胞系的人间充质干细胞(hMSCs)培养在gel-MA修饰的PdlLGA微球表面上,并使用Presto-Blue法研究不同表面修饰对细胞增殖的影响。数据分析表明,氧等离子体处理方法导致了凝胶-MA沉积的最高密度。这项研究支持氧等离子体处理,这是一种利用大分子(例如,凝胶-MA)修饰可注射PdlLGA微球表面的简便方法,以提高注射细胞的增殖速率,并有可能进一步移植组织特异性分子。

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