聚合物
溶解
无定形固体
溶解度
材料科学
氢键
化学工程
水溶液
混溶性
化学
高分子化学
分子
有机化学
工程类
作者
Baris Ugur,Nicholas J. Caggiano,Stephanie Monson,A. Bechtold,Yejoon Seo,Robert K. Prud’homme,Rodney D. Priestley,Michael Webb
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-08-20
卷期号:57 (17): 8287-8297
被引量:3
标识
DOI:10.1021/acs.macromol.4c01579
摘要
Cannabidiol (CBD) is viewed as a promising therapeutic agent against a variety of health ailments; however, its efficacy is limited by poor aqueous solubility. Amorphous solid dispersions (ASDs) can enhance the solubility of therapeutics by distributing them throughout a polymer matrix. In consideration of ASD formulations with CBD, we investigate the interactions of CBD with various polymers: poly(vinylpyrrolidone) (PVP), poly(vinylpyrrolidone)/vinyl acetate (PVP/VA) copolymer, hydroxypropyl methylcellulose phthalate (HPMCP), hydroxypropyl methylcellulose acetate succinate (HPMCAS), and poly(methyl methacrylate) (PMMA). Both the experiment and molecular dynamics simulation reveal diverse mixing behavior among the set of polymers. Detailed structural and nanoscale interaction analyses suggest that positive deviations from ideal mixing behavior arise from the formation of stable polymer–CBD hydrogen bonds, whereas negative deviations are associated with disruptions to the polymer–polymer hydrogen bond network. Polymer–water interaction analyses indicate the significance of polymer hydrophobicity that can lead to poor dissolution of CBD. These results have implications for drug dissolution rates based on how CBD and water interact with each polymer. Furthermore, these insights may be used to guide ASD formulations for CBD or other small-molecule therapeutic agents.
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