Chan TengIan, Ouyang Defang
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macau, China.
Asian J Pharm Sci. 2018 May;13(3):248-254. doi: 10.1016/j.ajps.2017.07.011. Epub 2017 Oct 23.
Dissolution molecular mechanism of solid dispersions still remains unclear despite thousands of reports about this technique. The aim of current research was to investigate the molecular dissolution mechanism of solid dispersions by molecular dynamics simulations. The formation of ibuprofen/polymer solid dispersions was modeled by the simulated annealing method. After that, the models of solid dispersions were immersed into the water box with 25-30 Å thicknesses and 50-100 ns MD simulations were performed to all systems. Simulation results showed various dissolution behaviors in different particle sizes and various polymers of solid dispersions. Small-sized particles of solid dispersions dissolved quickly in the water, while the large particles of PEG or PVP-containing solid dispersions gradually swelled in the dissolution process and drug molecules may aggregate together. In the dissolution process, the carboxylic groups of ibuprofen molecules turned its direction from polymer molecules to external water box and then the drug molecules left the polymer coils. At the same time, polymer coils gradually relaxed and became free polymer chains in the solution. In addition, solid dispersion with poloxamer could prevent the precipitate of drug molecules in the dissolution process, which is different from those of PEG or PVP-containing systems. This research provided us clear images of dissolution process of solid dispersions at the molecular level.
尽管关于固体分散体技术已有数千篇报道,但固体分散体的溶解分子机制仍不清楚。当前研究的目的是通过分子动力学模拟研究固体分散体的分子溶解机制。采用模拟退火方法模拟布洛芬/聚合物固体分散体的形成。之后,将固体分散体模型浸入厚度为25 - 30 Å的水盒中,并对所有体系进行50 - 100 ns的分子动力学模拟。模拟结果显示了不同粒径和不同聚合物的固体分散体的各种溶解行为。固体分散体的小尺寸颗粒在水中快速溶解,而含聚乙二醇(PEG)或聚乙烯吡咯烷酮(PVP)的固体分散体的大颗粒在溶解过程中逐渐膨胀,药物分子可能聚集在一起。在溶解过程中,布洛芬分子的羧基从聚合物分子方向转向外部水盒,然后药物分子离开聚合物链。同时,聚合物链逐渐松弛,在溶液中变成自由的聚合物链。此外,含泊洛沙姆的固体分散体在溶解过程中可防止药物分子沉淀,这与含PEG或PVP的体系不同。本研究在分子水平上为我们提供了固体分散体溶解过程的清晰图像。