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通过控制加载温度和时间来提高眼科透镜材料的药物持续释放性能。

Improving sustained drug delivery from ophthalmic lens materials through the control of temperature and time of loading.

机构信息

Centro de Química Estrutural, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.

Centro de Química Estrutural, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal; Departamento de Engenharia Mecânica, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.

出版信息

Eur J Pharm Sci. 2018 May 30;117:107-117. doi: 10.1016/j.ejps.2018.02.017. Epub 2018 Feb 14.

Abstract

Although the possibility of using drug-loaded ophthalmic lens to promote sustained drug release has been thoroughly pursued, there are still problems to be solved associated to the different alternatives. In this work, we went back to the traditional method of drug loading by soaking in the drug solution and tried to optimize the release profiles by changing the temperature and the time of loading. Two materials commercially available under the names of CI26Y and Definitive 50 were chosen. CI26Y is used for intraocular lenses (IOLs) and Definitive 50 for soft contact lenses (SCLs). Three drugs were tested: an antibiotic, moxifloxacin, and two anti-inflammatories, diclofenac and ketorolac. Sustained drug release from CI26Y disks for, at least 15 days, was obtained for moxifloxacin and diclofenac increasing the loading temperature up to 60 °C or extending the loading time till two months. The sustained release of ketorolac was limited to about 8 days. In contrast, drug release from Definitive 50 disks could not be improved by changing the loading conditions. An attempt to interpret the impact of the loading conditions on the drug release behavior was done using solid-state NMR and differential scanning calorimetry. These studies suggested the establishment of reversible, endothermic interactions between CI26Y and the drugs, moxifloxacin and diclofenac. The loading temperature had a slight effect on the mechanical and optical properties of drug loaded CI26Y samples, which still kept adequate properties to be used as IOL materials. The in vivo efficacy of CI26Y samples, drug loaded at 60 °C for two weeks, was predicted using a simplified mathematical model to estimate the drug concentration in the aqueous humor. The estimated concentrations were found to comply with the therapeutic needs, at least, for moxifloxacin and diclofenac.

摘要

虽然通过浸泡在药物溶液中使用载药眼科镜片来促进药物持续释放的可能性已经被彻底研究过,但仍然存在与不同选择相关的问题需要解决。在这项工作中,我们回到了通过浸泡在药物溶液中进行药物负载的传统方法,并尝试通过改变负载温度和时间来优化释放曲线。选择了两种商业上可获得的材料,分别名为 CI26Y 和 Definitive 50。CI26Y 用于眼内透镜(IOL),Definitive 50 用于软性隐形眼镜(SCL)。测试了三种药物:一种抗生素莫西沙星和两种消炎药双氯芬酸和酮咯酸。通过将负载温度提高到 60°C 或延长负载时间至两个月,CI26Y 盘可实现莫西沙星和双氯芬酸至少 15 天的持续药物释放。酮咯酸的持续释放时间限制在约 8 天。相比之下,改变负载条件不能改善 Definitive 50 盘的药物释放。使用固态 NMR 和差示扫描量热法尝试解释负载条件对药物释放行为的影响。这些研究表明,CI26Y 与莫西沙星和双氯芬酸等药物之间建立了可逆的、吸热相互作用。负载温度对负载药物的 CI26Y 样品的机械和光学性能有轻微影响,但仍保持足够的性能可用于 IOL 材料。使用简化的数学模型预测了在 60°C 下负载两周的 CI26Y 样品的体内疗效,以估计房水中的药物浓度。估计的浓度被发现符合治疗需求,至少对于莫西沙星和双氯芬酸是如此。

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