Instituto de Humanidades, Artes e Ciências, Universidade Federal do Sul da Bahia, Itabuna, Bahia, 45613-204, Brazil.
Instituto de Física, Universidade Federal da Bahia, Campus Universitário de Ondina, Salvador, Bahia, 40210-340, Brazil.
Eur Biophys J. 2020 Oct;49(7):571-589. doi: 10.1007/s00249-020-01463-8. Epub 2020 Sep 16.
Cyclodextrins (CDs) are well-known carriers for encapsulating hydrophobic molecules, while among cannabinoids, cannabidiol (CBD) has attracted considerable attention due to its therapeutic capability. In this framework, we employed molecular dynamics and docking techniques for investigating the interaction energy and thermodynamical issues between different CDs (α, β, and γ type) and CBD immersed in water and a solution mimicking a physiological environment. We quantified the energetic aspects, for different thermal conditions, in which both aqueous solutions interact with CBDs and CDs and the CBD-CDs complex itself. In order to approximate the physiological conditions, our simulations also included the mammalian temperature. The calculations revealed significant interaction energy between lactate and the CD surface and a movement of lactate toward CD as well. We observed an almost constant number of lactate molecules forming clusters without exhibiting a temperature dependence. Next, the degree of CBD-CDs complexation at four different temperatures was analyzed. The results showed that the complexation depends on the medium, becoming weaker with the temperature increment. Our findings highlighted that the entropy contribution is relevant for CBD-α-CD and CBD-β-CD, while CBD-γ-CD is practically insensitive to temperature changes for both solutions. In both water and artificial physiological solutions, the γ-CD appears more stable than the other complexes. Overall, CBD achieved partial encapsulation considering α-CD and β-CD, showing a temperature dependence, while γ-CD remained fully immersed no matter the thermal level assumed. We also discuss the pharmacological relevance and physiological implications of these findings.
环糊精(CDs)是众所周知的用于封装疏水分子的载体,而在大麻素中,由于其治疗能力,大麻二酚(CBD)引起了相当大的关注。在这个框架中,我们采用分子动力学和对接技术研究了不同 CDs(α、β 和 γ 型)与 CBD 在水中和模拟生理环境的溶液中的相互作用能量和热力学问题。我们量化了不同热条件下,水相溶液与 CBDs 和 CDs 以及 CBD-CDs 复合物本身之间的能量方面。为了近似生理条件,我们的模拟还包括哺乳动物温度。计算结果表明,乳酸盐与 CD 表面之间存在显著的相互作用能,并且乳酸盐向 CD 的迁移。我们观察到乳酸盐分子几乎没有形成簇,并且没有表现出温度依赖性。接下来,分析了四个不同温度下 CBD-CDs 复合物的程度。结果表明,复合物取决于介质,随着温度的升高而减弱。我们的发现强调了熵贡献对于 CBD-α-CD 和 CBD-β-CD 是相关的,而 CBD-γ-CD 对于两种溶液的温度变化几乎不敏感。在水和人工生理溶液中,γ-CD 比其他复合物更稳定。总的来说,考虑到 α-CD 和 β-CD,CBD 实现了部分封装,表现出温度依赖性,而 γ-CD 无论假设的热水平如何,都保持完全沉浸。我们还讨论了这些发现的药理学意义和生理意义。