Bayramoglu Gulay, Bitirim Verda, Tunali Yagmur, Arica Mehmet Yakup, Akcali Kamil Can
Biochemical Processing and Biomaterial Research Laboratory, Faculty of Sciences, Gazi University, 06500-Teknikokullar-Ankara, Turkey.
Laboratory of Stem Cell Research, Department of Molecular Biology and Genetics, Faculty Science, Bilkent University, 06800 Bilkent-Ankara, Turkey.
Mater Sci Eng C Mater Biol Appl. 2013 Mar 1;33(2):801-10. doi: 10.1016/j.msec.2012.11.004. Epub 2012 Nov 10.
Copolymerization of 2-hydroxyethylmethacrylate (HEMA) with glycidylmethacrylate (GMA) in the presence of α-α'-azoisobisbutyronitrile (AIBN) resulted in the formation of hydrogel films carrying reactive epoxy groups. Thirteen kinds of different molecules with pendant NH2 group were used for modifications of the p(HEMA-GMA) films. The NH2 group served as anchor binding site for immobilization of functional groups on the hydrogel film via direct epoxy ring opening reaction. The modified hydrogel films were characterized by FTIR, and contact angle studies. In addition, mechanical properties of the hydrogel films were studied, and modified hydrogel films showed improved mechanical properties compared with the non-modified film, but they are less elastic than the non-modified film. The biological activities of these films such as platelet adhesion, red blood cells hemolysis, and swelling behavior were studied. The effect of modified hydrogel films, including NH2, (using different aliphatic CH2 chain lengths) CH3, SO3H, aromatic groups with substituted OH and COOH groups, and amino acids were also investigated on the adhesion, morphology and survival of rat mesenchymal stem cells (MSCs). The MTT colorimetric assay reveals that the p(HEMA-GMA)-GA-AB, p(HEMA-GMA)-GA-Phe, p(HEMA-GMA)-GA-Trp, p(HEMA-GMA)-GA-Glu formulations have an excellent biocompatibility to promote the cell adhesion and growth. We anticipate that the fabricated p(HEMA-GMA) based hydrogel films with controllable surface chemistry and good stable swelling ratio may find extensive applications in future development of tissue engineering scaffold materials, and in various biotechnological areas.
在α,α'-偶氮二异丁腈(AIBN)存在的情况下,甲基丙烯酸2-羟乙酯(HEMA)与甲基丙烯酸缩水甘油酯(GMA)共聚,形成了带有反应性环氧基团的水凝胶薄膜。使用了13种带有侧链NH2基团的不同分子对p(HEMA-GMA)薄膜进行改性。NH2基团作为锚定结合位点,通过直接的环氧开环反应将官能团固定在水凝胶薄膜上。通过傅里叶变换红外光谱(FTIR)和接触角研究对改性水凝胶薄膜进行了表征。此外,还研究了水凝胶薄膜的力学性能,改性水凝胶薄膜与未改性薄膜相比,力学性能有所改善,但弹性不如未改性薄膜。研究了这些薄膜的生物活性,如血小板粘附、红细胞溶血和溶胀行为。还研究了改性水凝胶薄膜,包括NH2(使用不同脂肪族CH2链长度)、CH3、SO3H、带有取代OH和COOH基团的芳香族基团以及氨基酸,对大鼠间充质干细胞(MSCs)的粘附、形态和存活的影响。MTT比色法显示,p(HEMA-GMA)-GA-AB、p(HEMA-GMA)-GA-Phe、p(HEMA-GMA)-GA-Trp、p(HEMA-GMA)-GA-Glu配方具有优异的生物相容性,可促进细胞粘附和生长。我们预计,制备的具有可控表面化学性质和良好稳定溶胀率的基于p(HEMA-GMA)的水凝胶薄膜,可能会在组织工程支架材料的未来发展以及各种生物技术领域中得到广泛应用。