The Preparation of Curcumin Sustained-Release Solid Dispersion by Hot Melt Extrusion-I. Optimization of the Formulation

被引:22
作者
Fan, Wenling [1 ,2 ,3 ]
Zhu, Wenjing [1 ,2 ]
Zhang, Xinyi [1 ,2 ]
Di, Liuqing [1 ,2 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Lab Pharmaceut, Nanjing 210023, Peoples R China
[2] Nanjing Univ Chinese Med, Inst Jiangsu Engn Res Ctr Efficient Delivery Syst, Sch Pharm, Nanjing 210023, Peoples R China
[3] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resour, Sch Pharm, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
solid dispersion; curcumin; hot-melt extrusion; dissolution; sustained-release; WATER-SOLUBLE DRUGS; DISSOLUTION RATE; SOLUBILITY; DELIVERY; BIOAVAILABILITY; MISCIBILITY;
D O I
10.1016/j.xphs.2019.11.019
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purpose of this study was to optimize the formulation for developing curcumin sustained-release solid dispersion to increase the solubility of curcumin, delay drug release by hot-melt extrusion, and to explore the possibility of hot-melt extrusion for one-step preparation of insoluble drug sustained-release solid dispersion. The miscibility of curcumin and Eudragit RSPO and Eudragit RLPO were assessed by solubility parameter and melting point depression. Orthogonal test was used to optimize the formulation, based on the results of single-factor experiment, and the final optimal formulation: the ratio of the sustained-release carrier material RS/RL was 1:3, the ratio of drug and carrier was 1:6, and the porogen was used in an amount of 40% of the sustained-release carrier material. The curcumin solid dispersion of the best formulation had been prepared and had a significant sustained-release effect compared to the curcumin and the physical mixture. (C) 2020 Published by Elsevier Inc. on behalf of the American Pharmacists Association.
引用
收藏
页码:1242 / 1252
页数:11
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