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PEO--PCL/Tween 80/环糊精体系:从生物灵感的制备到盐酸罗匹尼罗可能的鼻内给药。

PEO--PCL/Tween 80/cyclodextrin systems: from bioinspired fabrication to possible nasal administration of ropinirole hydrochloride.

机构信息

Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Panepistimiopolis, 15771 Zografou, Greece.

School of Pharmacy, Chemistry Interdisciplinary Project (CHIP), University of Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

出版信息

J Mater Chem B. 2024 Jul 10;12(27):6587-6604. doi: 10.1039/d4tb00489b.

DOI:10.1039/d4tb00489b
PMID:38804576
Abstract

In this study, we designed and developed systems composed of poly(ethylene-oxide)--poly(ε-caprolactone) block copolymers of different molecular weights and compositions, non-ionic surfactant, and cyclodextrins. The innovation of this study lies in the combination of these diverse biomaterials to create biomimetic and bioinspired drug delivery supramolecular structures. The systems were formed by the thin-film hydration method. Extensive physicochemical and morphological characterization was conducted using differential scanning calorimetry, light scattering techniques, microcalorimetry analysis, high-resolution ultrasound spectroscopy, surface tension measurements, fluorescence spectroscopy, cryogenic transmission electron microscopy images, and cytotoxicity evaluation. These innovative hybrid nanoparticles were found to be attractive candidates as drug delivery systems with unique properties by encompassing the physicochemical and thermotropic properties of both classes of materials. Subsequently, Ropinirole hydrochloride was used as a model drug for the purpose of this study. These systems showed a high RH content (%), and diffusion experiments revealed that more than 90% of the loading dose was released under pH and temperature conditions that simulate the conditions of the nasal cavity. Promising drug release performance was observed with all tested formulations, worth further investigation to explore both permeation through the nasal mucosa and performance in an experimental animal model.

摘要

在这项研究中,我们设计和开发了由不同分子量和组成的聚(氧化乙烯)-聚(ε-己内酯)嵌段共聚物、非离子表面活性剂和环糊精组成的系统。本研究的创新之处在于将这些不同的生物材料结合在一起,创造仿生和生物启发的药物传递超分子结构。该系统是通过薄膜水合方法形成的。使用差示扫描量热法、光散射技术、微量热分析、高分辨率超声光谱法、表面张力测量、荧光光谱法、低温传输电子显微镜图像和细胞毒性评估对系统进行了广泛的物理化学和形态学表征。这些创新型混合纳米粒子被发现是具有独特性质的药物传递系统的有吸引力的候选物,包含了两类材料的物理化学和热致性质。随后,盐酸罗匹尼罗被用作本研究的模型药物。这些系统表现出高 RH 含量(%),扩散实验表明,在模拟鼻腔条件的 pH 值和温度条件下,超过 90%的加载剂量被释放。所有测试配方都表现出有前途的药物释放性能,值得进一步研究,以探索其在鼻黏膜渗透和实验动物模型中的性能。

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