自组装的多层奇托-胰岛素纳米颗粒集成到双层溶解微针中,用于持续的输送
Melbha Starlin Chellathurai1, Syed Mahmood2, Zarif Mohamed Sofian3
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Universiti Malaya, Kuala Lumpur 50603, Malaysia.
International journal of biological macromolecules
|June 27, 2025
概括
这项研究开发了口服微针,用于使用层次 (LbL) 纳米粒子输送胰岛素. 这种方法增强了胰岛素的负载,稳定性,并为改善口服药物递送提供持续释放.
科学领域:
- 生物材料科学 生物材料科学
- 纳米技术纳米技术
- 药物运输 药物运输 药物运输
背景情况:
- 传统的口服胰岛素输送面临着低生物可用性和透性问题的挑战.
- 微针技术为跨粘膜药物输送提供了一个有希望的替代方案.
研究的目的:
- 开发和描述口服微针,以提高胰岛素负载,稳定性和持续释放.
- 调查Layer-by-Layer (LbL) 自组装纳米颗粒用于口服胰岛素输送的潜力.
主要方法:
- 利用受控的离子凝来制备核心涂层纳米粒子.
- 雇佣层次加载 (LbL) 用奇托和胰岛素.
- 使用可生物降解的聚合物制成的纳米颗粒变成微针.
- 评估了纳米粒子稳定性,胰岛素释放动力学和微针机械强度.
主要成果:
- 在固态纳米粒子中实现了高胰岛素负载和提高了胰岛素的稳定性.
- 在pH值6.8.8下,可在24小时内持续释放胰岛素.
- 在纳米粒子层内确认了成功的细胞内化和胰岛素的保护.
- 微针表现出足够的强度,可以通过粘膜传递.
结论:
- 在口服微针中集成的LbL组装纳米颗粒显示出有效的胰岛素输送的潜力.
- 这种方法克服了传统的口服输送限制,并提供持续的药物释放.
- 该技术可适应通过微针传递其他生物制剂,如疫苗和激素.
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