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可注射的含有脂质体的点击水凝微粒,用于释放宏分子载荷
Luisa L Palmese1, Paige J LeValley2, Lina Pradhan2
1Materials Science and Engineering, University of Delaware, Newark, DE, USA. akloxin@udel.edu.
Soft matter
|January 30, 2024
概括
我们使用微流体技术开发了可注射的聚乙烯基醇 (PEG) 基微凝和脂微凝. 这些微凝可以封装并维持治疗载荷的释放长达三周.
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
- 微流体学 微流体学
背景情况:
- 水凝微粒 (微凝) 由于其可注射性和模块化性,为生物应用提供了优势.
- 现有的微凝生产方法需要扩展以满足各种治疗需求.
研究的目的:
- 建立一种微流体方法,以生产基于聚乙烯糖醇 (PEG) 的微凝和含有脂质体的微凝 (lipo-microgels).
- 描述开发的微凝的物理化学特性和货物输送能力.
主要方法:
- 基于滴滴的微流体被用来通过迈克尔类型的添加反应合成基于PEG的微凝和脂质微凝.
- 分析了微凝大小,形态,脂质体存在,机械特性 (AFM) 和货物释放动力学.
主要成果:
- 均的球形微凝 (74 ± 16 微米) 和脂质微凝 (82 ± 25 微米) 已成功产生,通过显微镜确认.
- 风病学分析证实了微凝的可注射性.
- 持续释放模型货物 (FITC-Dextran 5 kDa) 和蛋白质 (马类肌球蛋白) 观察到长达3周,蛋白质结构保持.
结论:
- 微流体方法提供了一个多功能平台,用于创建可注射的基于PEG的微凝和脂微凝.
- 这些微凝具有保护和控制治疗载荷释放的潜力,包括蛋白质.
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