Liane Meneses, Dimitra Antonia Bagaki, Ana Roda, Alexandre Paiva, Ana Rita C Duarte
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引用次数: 0
摘要
可注射水凝胶具有微创、易于应用和空隙填充等特性,因此已被广泛研究。在这项工作中,我们测试了制备新型凝胶(即共晶凝胶)的可能性,在这种凝胶中,水被天然深共晶体系(NADES)取代,从而使其具有更长的稳定性。我们使用辣根过氧化物酶(HRP)作为催化剂和明胶-苯酚共轭聚合物,通过酶介导交联法制备了甜菜碱-甘油 1:2 共晶凝胶。与需要较高酶浓度(15 U mL-1)才能在 2 分钟内凝胶的水凝胶相比,使用 10 U mL-1 和 5 U mL-1 的 HRP 可分别获得 30 秒和 50 秒的凝胶时间。最后,在聚合物基质中加入酮洛芬,并进行了释放研究。NADES 的存在对药物负载凝胶的配制至关重要,这种凝胶能在 10 天内释放高达 70% 的药物,因此可以得出结论,这些共晶凝胶可作为基质在水介质中控制酮洛芬的给药。对优特凝胶各成分进行的体外生物评估表明,它们没有细胞毒性作用,这表明它们具有潜在的生物相容性。
Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery.
Injectable hydrogels have been extensively studied due to their minimally invasive properties, ease of application, and void-filling properties. In this work, we tested the possibility to prepare a new type of gels, so called eutectogels, where water is replaced by a natural deep eutectic system (NADES), conferring it longer stability. Eutectogels based on betaine : glycerol 1 : 2, were prepared by enzymatic mediated crosslinking, using horseradish peroxidase (HRP) as catalyst and gelatine-phenol conjugated polymer. In comparison to hydrogels, that required higher enzyme concentration (15 U mL-1) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL-1 of HRP, with gelation times of 30 and 50 seconds, respectively. Finally, ketoprofen was loaded into the polymeric matrix, and release studies were conducted. The presence of NADES was essential for the formulation of the drug loaded gel, which was able to release up to 70% of the drug within 10 days, therefore, it was possible to conclude that these eutectogels work as matrix for the controlled delivery of ketoprofen in aqueous medium. The in vitro biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.