Cao Yizheng, Teng Jing, Selbo Jon
Solid State Chemical Information (SSCI), a Division of Albany Molecular Research Inc., West Lafayette, IN 47906, USA.
Pharmaceuticals (Basel). 2017 Nov 9;10(4):88. doi: 10.3390/ph10040088.
Epigallocatechin gallate (EGCG) has been recognized as the most prominent green tea extract due to its healthy influences. The high instability and low bioavailability, however, strongly limit its utilization in food and drug industries. This work, for the first time, develops amorphous solid dispersion of EGCG to enhance its bioavailability and physical stability. Four commonly used polymeric excipients are found to be compatible with EGCG in water-dioxane mixtures via a stepwise mixing method aided by vigorous mechanical interference. The dispersions are successfully generated by lyophilization. The physical stability of the dispersions is significantly improved compared to pure amorphous EGCG in stress condition (elevated temperature and relative humidity) and simulated gastrointestinal tract environment. From the drug release tests, one of the dispersions, EGCG-Soluplus 50:50 (/) shows a dissolution profile that only 50% EGCG is released in the first 20 min, and the remains are slowly released in 24 h. This sustained release profile may open up new possibilities to increase EGCG bioavailability via extending its elimination time in plasma.
表没食子儿茶素没食子酸酯(EGCG)因其对健康的影响而被公认为最主要的绿茶提取物。然而,其高不稳定性和低生物利用度严重限制了它在食品和制药行业的应用。这项工作首次开发了EGCG的无定形固体分散体,以提高其生物利用度和物理稳定性。通过在剧烈机械搅拌辅助下的逐步混合方法,发现四种常用的聚合物辅料在水-二氧六环混合物中与EGCG具有相容性。通过冷冻干燥成功制备了分散体。与纯无定形EGCG相比,在应激条件(高温和相对湿度)和模拟胃肠道环境下,分散体的物理稳定性显著提高。从药物释放试验来看,其中一种分散体EGCG-固体分散体50:50(/)显示出一种溶出曲线,即在最初20分钟内仅释放50%的EGCG,其余部分在24小时内缓慢释放。这种缓释曲线可能为通过延长其在血浆中的消除时间来提高EGCG生物利用度开辟新的可能性。