Mono-Dendronized β‑Cyclodextrin Derivatives as Multitasking Containers for Curcumin. Impacting Its Solubility, Loading, and Tautomeric Form

• Published in: The journal of physical chemistry. B Vol. 126; no. 7; pp. 1529 - 1538
• Main Authors: Cabrera-Quiñones, Neyra Citlali, López-Méndez, Luis José, Ramos, Estrella, Rojas-Aguirre, Yareli, Guadarrama, Patricia
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 24.02.2022
• Subjects: Antioxidants - chemistry; B: Biomaterials and Membranes; beta-Cyclodextrins - chemistry; Curcumin - chemistry; Solubility; Water - chemistry
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/acs.jpcb.1c09811

In this study, three mono-dendronized β-cyclodextrin (βCD) derivatives (βCD-1G, βCD-2G, and βCD-3G) were used as multitasking containers of curcumin (CUR) to influence its aqueous solubility and tautomerism, both of which are related to its biological activity. We evaluated the relevant physicochemical properties of these containers associated with their potential hosting capacity. All mono-dendronized derivatives exhibited enhanced solubility in different solvents, including water, in comparison with native βCD. Gas-phase geometry optimizations by density functional theory (DFT) confirmed that none of the dendrons blocked the passage of CUR into the βCD cavity, and depending on the generation, different preorganization scenarios were promoted before complexation. Phase solubility diagrams showed that all the dendronized containers have superior performance for solubilizing CUR compared to native βCD. We proved that coprecipitation is most efficient than lyophilization for forming inclusion complexes (ICs) with dendronized containers. Even though βCD-3G with the largest 3G dendron exhibited the highest CUR loading, the complexation of CUR with βCD-2G provided the supramolecular system that contains CUR preferentially in its diketo tautomer, which is known for its antioxidant activity.