Arica M Yakup, Bayramoglu Gülay, Arica Betül, Yalçin Emine, Ito Koichi, Yagci Yusuf
Biochemical Processing and Biomaterial Research Laboratory, Faculty of Science, Kirikkale University, 71450-Yahşihan-Kirikkale, Turkey.
Macromol Biosci. 2005 Oct 20;5(10):983-92. doi: 10.1002/mabi.200500091.
The aim of this study was to synthesize and characterize a novel biocompatible polymeric membrane system and demonstrate its potential use in various biomedical applications. Synthetic hydrogels based on poly(hydroxyethyl methacrylate), poly(HEMA), have been widely studied and used in biomedical fields. A novel copolymer hydrogel was prepared in the membrane form using 2-hydroxyethyl methacrylate monomer (HEMA) and a macromonomer p-vinylbenzyl-poly(ethylene oxide) (V-PEO) via photoinitiated polymerization. A series of poly(HEMA/V-PEO) copolymer membranes with different compositions was prepared. The membranes were characterized using infrared, thermal and SEM analysis. The thermal stabilities of the copolymer membranes were found to be lowered by an increase in the ratio of macromonomer (V-PEO) in the membrane structure. Because of the incorporation of PEO segments, the copolymers exhibited significantly higher hydrophilic surface properties than pure poly(HEMA), as demonstrated by contact angle measurements. Equilibrium swelling studies were conducted to investigate the swelling behavior of the membranes. The equilibrium water uptake was reached in about 4 h. Moreover, the blood protein adsorption and platelet adhesion were significantly reduced on the surface of the PEO containing copolymer membranes compared to control pure poly(HEMA). Drug release experiments were performed in a continuous release system using model drug (vancomycin) loaded copoly(HEMA/V-PEO) membranes. A specific poly(HEMA/V-PEO) membrane formulation possessing the highest PEO content (with a HEMA:V-PEO (mmol:mmol) feed ratio of 112:1 and loaded with 40 mg antibiotic/g polymer) released about 81% of the total loaded drug in 24 h at pH 7.4. This membrane composition provided the best results and can be considered as a potential candidate for a transdermal antibiotic carrier and various biomedical and biotechnological applications.
本研究的目的是合成并表征一种新型生物相容性聚合物膜系统,并展示其在各种生物医学应用中的潜在用途。基于聚甲基丙烯酸羟乙酯(poly(hydroxyethyl methacrylate),poly(HEMA))的合成水凝胶已在生物医学领域得到广泛研究和应用。通过光引发聚合反应,使用甲基丙烯酸羟乙酯单体(HEMA)和大分子单体对乙烯基苄基聚环氧乙烷(V-PEO)制备了一种新型共聚物水凝胶膜。制备了一系列不同组成的聚(HEMA/V-PEO)共聚物膜。使用红外、热分析和扫描电子显微镜分析对这些膜进行了表征。发现共聚物膜的热稳定性会因膜结构中大分子单体(V-PEO)比例的增加而降低。由于引入了PEO链段,通过接触角测量表明,共聚物表现出比纯聚(HEMA)显著更高的亲水性表面性质。进行了平衡溶胀研究以考察膜的溶胀行为。约4小时达到平衡吸水率。此外,与对照纯聚(HEMA)相比,含PEO的共聚物膜表面的血液蛋白吸附和血小板粘附显著降低。使用载有模型药物(万古霉素)的聚(HEMA/V-PEO)共聚物膜在连续释放系统中进行了药物释放实验。一种具有最高PEO含量的特定聚(HEMA/V-PEO)膜配方(HEMA:V-PEO(毫摩尔:毫摩尔)进料比为112:1,每克聚合物负载40毫克抗生素)在pH 7.4条件下24小时内释放了约81%的总负载药物。这种膜组成提供了最佳结果,可被视为透皮抗生素载体以及各种生物医学和生物技术应用的潜在候选材料。