Department of Chemistry, Loyola University Chicago , 1032 W. Sheridan Road, Chicago, Illinois 60660, USA.
Mol Pharm. 2013 Mar 4;10(3):905-17. doi: 10.1021/mp4000212. Epub 2013 Feb 14.
In order to gain molecular level understanding of drug dissolution into aqueous media, we report the first molecular dynamics (MD) simulation of a drug crystal dissolving. The simulation was performed for acetaminophen crystal Form I dissolving in 0.15 M aqueous NaCl solution at 37 °C. The 10 ns simulation revealed interesting details of the dissolution process. Dissolution of the molecules from the crystal surface is far from a random process. On the contrary, the order in which molecules enter the solution depends on their initial positions in or on the crystal. Molecules located on the corners and edges dissolved first followed by those located on {100}, {010}, and {001) surfaces with slight variation. This corner and edge effect that has been observed in our real dissolution experiment conducted under polarized light microscope was successfully predicted at molecular scale by the MD simulation. Further analyses identified the underlying mechanism: the differences in the molecular interaction energetics between the drug and water molecules. The molecules located on corners and edges of the parallelepiped crystal are not as tightly bound to their surrounding neighbors as those located in other positions, but they are more strongly interacting with the surrounding water molecules. The extent of molecular release is strongly correlated with the interplay between interaction forces with solvent molecules and with other drug molecules in the crystal lattice. These findings, especially the significant "corner and edge effect", will help us gain additional fundamental understanding in the relationship between dissolution rate and particle size and morphology and, thus, are very relevant in the context of particle size reduction in delivering poorly water-soluble compounds. This study has also demonstrated that MD simulation is a powerful tool in studying dissolution phenomena.
为了从分子水平上理解药物在水介质中的溶解,我们首次报道了药物晶体溶解的分子动力学(MD)模拟。该模拟在 37°C 下进行,研究了对乙酰氨基酚晶型 I 在 0.15 M 水溶液中的溶解过程。10ns 的模拟揭示了溶解过程的有趣细节。从晶体表面溶解的分子远非随机过程。相反,分子进入溶液的顺序取决于它们在晶体中的初始位置。位于角和棱上的分子首先溶解,然后是位于{100}、{010}和{001}表面的分子,略有变化。这种在我们在偏光显微镜下进行的实际溶解实验中观察到的角和棱效应,在分子尺度上被 MD 模拟成功预测。进一步的分析确定了潜在的机制:药物和水分子之间分子相互作用的能量差异。位于平行六面体晶体角和棱上的分子与其周围相邻分子的结合不如位于其他位置的分子紧密,但它们与周围水分子的相互作用更强。分子释放的程度与溶剂分子和晶格中其他药物分子之间相互作用力的相互作用密切相关。这些发现,尤其是显著的“角和棱效应”,将帮助我们在溶解速率与颗粒尺寸和形态之间的关系方面获得更多的基本理解,因此在降低难溶性化合物的颗粒尺寸方面非常相关。本研究还表明,MD 模拟是研究溶解现象的有力工具。