Experimental and molecular docking investigation of the inclusion complexes between 20(S)-protopanaxatriol and four modified β-cyclodextrins

• Published in: Carbohydrate research 2021-02, Vol.500, p.108256-108256, Article 108256
• Main Authors: Zhu, Fang-Dao, Zhang, Zhao-Hua, Chi, Shao-Ming, Chen, Si-Ling, Wang, Yu-Fei, Zhu, Hong-You, Lei, Ze, Zhao, Yan
• Format: Article
• Language: English
• Subjects: 20(S)-Protopanaxatriol; Binding mode; Inclusion complex; Modified β-cyclodextrins; Molecular docking; Solubilization
• ISSN: 0008-6215; 1873-426X
• DOI: 10.1016/j.carres.2021.108256

20(S)-Protopanaxatriol (PPT) is a type of ginsenoside isolated from panax notoginseng or ginseng, which is an essential ingredient in functional food, healthcare products and traditional medicine. However, the research and development of PPT are restricted due to its poor solubility. To circumvent the associated problems, a novel bridged-bis [6-(2,2’-(ethylenedioxy) bis (ethylamine))-6-deoxy-β-CD] (H4) was successfully synthesized. The four inclusion complexes of the mono-[6-(1,4-butanediamine)-6-deoxy-β-CD] (H1), mono-[6-(2,2’-(ethylenedioxy) bis (ethylamine)-6-deoxy-β-CD] (H2) and their corresponding bridged bis(β-CD)s (H3, H4) with PPT were prepared and studied by UV, 1H NMR, 2D ROESY, FT-IR, XRD and SEM technology. The UV-spectrometric titration showed that H1-4 and PPT formed 1:1 inclusion complexes and the binding constants were 297.61, 322.25, 937.88 and 1742 M−1, respectively. It was further revealed that the size/shape-matching relationship, hydrophobic interactions and hydrogen bond interactions play the crucial role in determining the stability of H1-4/PPT inclusion complexes. The solubility of PPT was evidently enhanced by193, 265, 453 and 593 times after the formation of inclusion complexes with H1-4, respectively. Furthermore, molecular docking was used to verify the inclusion mode of H4/PPT inclusion complex and also to investigate the stability of H4/PPT in water phase. The molecular simulation results agreed well with the experimental results. This research provides an effective way to obtain novel PPT-based functional food and healthcare products. [Display omitted] •Four novel H1-4/PPT inclusion complexes were prepared and characterized.•The binding ability and inclusion modes of four inclusion complexes were discussed.•Aqueous solubility of PPT significantly increased by complexation with H1-4.•Molecular dynamic simulations corroborated experimental results.•Provided reference value for the application of PPT.