Interactions between β-cyclodextrin and tea catechins, and potential anti-osteoclastogenesis activity of the (-)-epigallocatechin-3-gallate-β-cyclodextrin complex. 2019

Huanhuan Xu, and Titi Liu, and Jing Xu, and Jin Li, and Fei Chen, and Zemin Xiang, and Yewei Huang, and Dongying Zhang, and Lihong Hu, and Banglei Zhang, and Chengting Zi, and Xuanjun Wang, and Jun Sheng
Key Laboratory of Pu-er Tea Science, Ministry of Education, Yunnan Agricultural University Kunming 650201 China zichengting@126.com wangxuanjun@gmail.com shengjunpuer@163.com +86-871-65226058 +86-871-65226058.

Galloylated catechins, the most important secondary metabolites in green tea including (-)-epigallocatechin-3-gallate (EGCG) and (-)-epicatechin-3-gallate, constitute nearly 75% of all tea catechins and have stronger health effects than non-galloylated catechins such as (-)-epigallocatechin and (-)-epicatechin. EGCG is the most abundant, active, and thoroughly investigated compound in green tea, and its bioactivity might be improved by complexing with β-cyclodextrin (β-CD). We investigated interactions between four catechins and β-CD in a PBS buffer solution of pH 6.5 at 25 °C using biolayer interferometry and isothermal titration calorimetry, and to determine whether β-CD could enhance the anti-osteoclastogenesis effect of EGCG. β-CD could directly bind galloylated catechins at a stoichiometric ratio close to 1 : 1, with high specificities and affinities, and these inclusion interactions were primarily enthalpy-driven processes. We synthesized the EGCG-β-CD complex and identified it using infrared radiation and nuclear magnetic resonance spectra. Interestingly, we revealed that the EGCG-β-CD complex could inhibit osteoclastogenesis significantly more than EGCG.

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