制造可调整尺寸的PEG-PLGA微粒,用于控制药物释放应用
Paul Nana Kwame Sagoe1, Eduardo José Machado Velázquez2, Yohely Maria Espiritusanto1
1Department of Biomedical and Chemical Engineering, Bioinspired Syracuse: Institute for Material and Living System, Syracuse University, Syracuse, NY 13244, USA.
Molecules (Basel, Switzerland)
|September 28, 2023
概括
一种新的同轴流相分离方法可以精确控制聚乙烯甘 - 聚乳酸 - 同甘酸 (PEG-PLGA) 微粒大小和形态,以改进药物递送系统.
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:
- 聚合物微粒,特别是PEG-PLGA,是重要的药物载体.
- 现有的方法在精确的尺寸调整,统一性和可重复性方面扎.
- 挑战包括控制颗粒大小,形态,产量和药物载荷能力.
研究的目的:
- 开发一种可调节,单分散微粒合成的可扩展方法.
- 研究工艺参数对微粒子特性的影响.
- 优化微粒制造以提高药物加载和释放.
主要方法:
- 微粒子合成的同轴流相分离技术.
- 系统评估聚合物度,速,表面活性剂度和流量.
- 纳入光染料以模拟水友性和疏水性药物.
主要成果:
- 速和聚合物度显著影响颗粒大小和分布.
- 表面活性剂度是控制粒子形态学的关键.
- 实现了可调节的颗粒大小 (5-50μm),具有高单分散性和批量复制性.
- 证明了各种形态和度的可扩展性和可调性.
- 尽管聚合物度和体积的数量有序变化,但在配方中实现了可比的颗粒大小 (5-7μm).
- 聚合物数量影响药物加载,封装效率和释放动力学.
结论:
- 新的同轴流相分离方法可以精确控制PEG-PLGA微粒制造.
- 这种技术允许调整大小,改进单分散性和批次到批次的可重复性.
- 这些发现为制造含有药物的微粒提供了一个框架,这些微粒具有针对特定输送应用的定制性质.
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