从PLGA微粒中释放的药物可以通过周围的水凝来减缓
L A Lefol1, P Bawuah2, J A Zeitler2
1Univ. Lille, Inserm, CHU Lille, U1008, Lille F-59000, France.
International journal of pharmaceutics: X
|December 26, 2023
概括
当在水凝中封装时,从聚乳-同-甘油酸 (PLGA) 微粒中释放药物的速度明显较慢. 水凝屏障阻碍了胀和药物扩散,延长了布洛芬的释放时间.
科学领域:
- 生物材料科学 生物材料科学
- 药物输送系统 药物输送系统
- 聚合物化学 聚合物化学
背景情况:
- 聚乳-同-甘油酸 (PLGA) 微粒广泛用于控制药物输送.
- 了解影响药物释放动态的因素对于优化治疗疗效至关重要.
- 水凝可以作为组织模仿剂,可能改变药物释放概况.
研究的目的:
- 为了研究周围的水凝对PLGA微粒中的布洛芬释放的影响.
- 阐明在水凝的存在下改变药物释放背后的机制.
- 为了比较水凝环境中的药物释放与激动的缓冲器.
主要方法:
- 使用乳液溶剂提取/蒸发来制备含有布洛芬的PLGA微粒.
- 使用光学显微镜,SEM,DSC,XRD和X射线μCT进行微粒体形态和微观结构的表征.
- 测量伊布洛芬释放动力学在阿加罗斯水凝和激动酸盐缓冲体 (pH 7.4) 中.
主要成果:
- PLGA微粒表现出光滑的表面和内部多孔网络.
- 与激动缓冲器 (几天) 相比,在阿加罗斯凝中 (完全释放两周) 的布洛芬释放显著较慢.
- 水凝的存在可能阻碍了颗粒膨胀和对流流引起的损伤,减缓了药物扩散.
结论:
- 周围的水凝可以大大降低PLGA微粒的药物释放速度.
- 由水凝引起的硬质障碍和减少胀是减缓药物流动性的关键因素.
- 这一发现对设计针对特定组织环境的药物递送系统有影响.
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