Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, University of Lisbon, 1049-001, Lisboa, Portugal.
Mechanical Engineering Department and IDMEC, Instituto Superior Técnico, University of Lisbon, 1049-001, Lisboa, Portugal.
J Biomed Mater Res B Appl Biomater. 2017 Oct;105(7):1799-1807. doi: 10.1002/jbm.b.33715. Epub 2016 May 18.
In this article, liposome-based coatings aiming to control drug release from therapeutic soft contact lenses (SCLs) materials are analyzed. A PHEMA based hydrogel material loaded with levofloxacin is used as model system for this research. The coatings are formed by polyelectrolyte layers containing liposomes of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and DMPC + cholesterol (DMPC + CHOL). The effect of friction and temperature on the drug release is investigated. The aim of the friction tests is to simulate the blinking of the eyelid in order to verify if the SCLs materials coated with liposomes are able to keep their properties, in particular the drug release ability. It was observed that under the study conditions, friction did not affect significantly the drug release from the liposome coated PHEMA material. In contrast, increasing the temperature of release leads to an increase of the drug diffusion rate through the hydrogel. This phenomenon is recorded both in the control and in the coated samples. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 1799-1807, 2017.
本文分析了旨在控制治疗性软性隐形眼镜(SCL)材料中药物释放的基于脂质体的涂层。以载左氧氟沙星的 PHEMA 水凝胶材料为模型体系进行了这项研究。这些涂层由含有 1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)和 DMPC+胆固醇(DMPC+CHOL)脂质体的聚电解质层形成。研究了摩擦和温度对药物释放的影响。摩擦试验的目的是模拟眨眼,以验证涂有脂质体的 SCL 材料是否能够保持其特性,特别是药物释放能力。结果表明,在研究条件下,摩擦对脂质体涂覆的 PHEMA 材料中药物的释放没有显著影响。相比之下,释放温度的升高会导致药物通过水凝胶的扩散速率增加。这种现象在对照和涂层样品中都有记录。© 2016 Wiley Periodicals, Inc. J 生物材料研究杂志 B:应用生物材料,105B:1799-1807,2017。