针对pentamidine针对CD44过度表达细胞使用化脂聚合物混合纳米颗粒
Ilaria Andreana1, Marta Chiapasco1, Valeria Bincoletto1
1Dipartimento di Scienza e Tecnologia del Farmaco, Università di Torino, Torino, Italy.
Drug delivery and translational research
|May 6, 2024
概括
研究人员开发了新型混合纳米载体,使用聚乳糖合糖酸 (PLGA) 和氨酸 (HA) 进行向药物输送. 这些纳米颗粒显示了增强的药物负载,并选择性地向过度表达CD44受体的癌细胞.
科学领域:
- 生物材料科学 生物材料科学
- 纳米技术 纳米技术
- 药物输送系统 药物输送系统
背景情况:
- 可生物降解的纳米载体为控制和向的药物释放提供了潜力.
- 脂质体和聚合物纳米粒子是已建立的药物递送系统.
- 混合纳米载体可以结合不同平台的优势,以提高效率和定位.
研究的目的:
- 为了制定混合纳米载体,将聚乳-co-糖酸 (PLGA) 和氨酸 (HA) 结合起来,用于主动向.
- 为了利用离子相互作用来增强药物封装,使用胺胺 (PTM-B) 作为模型药物.
- 评估混合纳米载体对癌细胞的向传递和细胞毒性.
主要方法:
- 用氨酸-脂联合体 (HA-DPPE) 配制PLGA纳米颗粒,用于HA的表面固.
- 通过负电荷的PLGA/HA和正电荷的胺素之间的离子配对来进行药物加载.
- 纳米载体大小,泽塔潜力,内部结构和封装效率的表征.
- 细胞吸收和细胞毒性对CD44过度表达的癌细胞的体外评估.
主要成果:
- 成功制备了大小小小于150nm的混合纳米载体,zeta潜力为-35mV.
- 通过离子配对实现了胺胺的高封装效率 (90%).
- 在过度表达CD44.4的癌细胞上证明了优选的细胞吸收和受体介导的细胞毒性.
- 确认了纳米颗粒的CD44依赖细胞内化.
结论:
- 开发的PLGA/HA-DPPE混合纳米载体代表了针对药物输送的有希望的平台.
- 与传统的PLGA纳米粒子相比,离子配对方法提高了药物载荷能力.
- CD44介导的向机制可以选择性地传递给癌细胞,从而有可能改善治疗结果.
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