在控制的抗生素释放中应用的氨酸-酸盐均结构与聚酸涂层
Anna Trusek1, Maciej Grabowski1, Omoyemi Ajayi1
1Department of Micro, Nano and Bioprocess Engineering, Wroclaw University of Science and Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland.
Gels (Basel, Switzerland)
|July 28, 2023
概括
化学交叉链接的氨酸-氨酸酸基凝,涂有聚酸,显著延长药物释放. 这种控制释放药物递送系统提高了治疗牙科和伤口护理中局部感染的抗生素疗效.
科学领域:
- 生物材料科学 生物材料科学
- 聚合物化学 聚合物化学
- 药物输送系统 药物输送系统
背景情况:
- 水凝是局部感染的有希望的生物相容和生物降解药物载体.
- 水凝的一个主要限制是它们的药物释放速度很快.
- 控制释放系统对于持续的治疗效果至关重要.
研究的目的:
- 开发一种新的可控释放药物载体,该载体是基于氨酸-酸酸盐水凝.
- 通过化学交联和聚合物涂层来增强水凝载体的药物释放特征.
- 评估这些载体在传递阿莫西西林,甲尼达和多西环林等抗生素方面的潜力.
主要方法:
- 化学交叉链接的氨酸-氨酸 (HA-SAL) 使用1-乙基-3-(3-二甲基氨基) -1-碳二胺化物 (EDC).
- 将交联的HA-SAL水凝载体涂上一个聚酸聚合物层.
- 研究聚酸涂层对药物释放动态的影响.
主要成果:
- 聚酸涂层显著降低了水凝载体的质量流.
- 与未涂层的水凝相比,药物释放时间延长了大约40倍.
- 修改后的水凝显示出持续递送阿莫西西林,甲尼达和多西环林的潜力.
结论:
- 化学交叉连接的HA-SAL水凝涂有聚酸,为控制药物释放提供了一个可行的策略.
- 这种方法有效地克服了传统水凝的快速释放限制.
- 开发的系统在牙科和伤口治疗中显示出局部抗生素输送的前景.
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