基于聚氧乙烯 (POE) 的非离子表面活性剂的物理化学表征,用于单个和混合的细胞环境中增强抗癌药物的溶解
Virendra Prajapati1, Yashika Tomar2, Gautam Singhvi2
1Department of Chemistry, Sardar Vallabhbhai National Institute of Technology (SVNIT), Ichchhanath Dumas Road, Keval Chowk, Surat-395007, Gujarat, India. ketankuperkar@gmail.com.
Physical chemistry chemical physics : PCCP
|September 5, 2025
概括
这项研究使用Soluplus®和其他表面活性剂探索纳米细胞的形成,揭示了增强药物溶解和控制释放的协同效应. 这项研究强调Soluplus®
科学领域:
- 体和表面科学
- 材料科学
- 制药科学
背景情况:
- 像Soluplus®这样的两接种共聚物对于制备难溶药物至关重要.
- 了解单一和混合表面活性剂系统中的细胞行为是药物输送应用的关键.
- 基于聚氧乙烯 (POE) 的非离子表面活性剂表现出不同的溶液特性,受度和温度的影响.
研究的目的:
- 研究Soluplus®与各种基于POE的非离子表面活性剂相结合的纳米级细胞形成和溶液行为.
- 描述表面活性剂混合对细胞形态,稳定性和药物溶解能力的影响.
- 从这些纳米系统中评估Quercetin的体外药物释放动力学 (QCT).
主要方法:
- 测量溶液粘度和粘弹性.
- 用于微粒大小和形状分析的动态光散射 (DLS) 和小角度中子散射 (SANS).
- 紫外线可见 (UV-vis) 光谱测量奎尔西的溶解 (QCT).
主要成果:
- Soluplus®形成大型球状,而P123则表现出热可逆的凝结和形态转变.
- 混合 Soluplus® 系统表现出协同作用,显著增加云点并增强 QCT 溶解.
- 希古奇模型最好地描述了体外药物释放,表明了扩散控制机制.
结论:
- 基于Soluplus®的混合体系统提供了优异的溶解和控制的疏水药物释放,如QCT.
- 在特定的Soluplus®混合物中的协同作用对制药配方开发有利.
- 这些纳米级组件为增强疏水活性药物成分提供了一个有前途的平台.
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