姜黄素
溶解
无定形固体
过饱和度
结晶
差示扫描量热法
化学工程
化学
溶解度
溶解试验
材料科学
聚合物
色散(光学)
有机化学
生物化学
工程类
物理
光学
热力学
生物制药分类系统
作者
Liang Qi,Yiru Wang,Yue-Yi Deng
出处
期刊:PubMed
日期:2019-08-01
卷期号:44 (15): 3305-3311
被引量:1
标识
DOI:10.19540/j.cnki.cjcmm.20190516.301
摘要
To enhance in vitro dissolution of Cur by preparing Cur solid dispersions. The ability of HPMCAS-HF,HPMCAS-MF,HPMCAS-LF and PVPK30 to maintain supersaturated solution was investigated by supersaturation test. Amorphous solid dispersions were prepared by the solvent-evaporation method. The prepared samples were characterized using infrared spectroscopy( IR) and differential scanning calorimetry( DSC),and in vitro dissolution was investigated. DSC and IR results showed that in 1 ∶3 and 1 ∶9 solid dispersions,Cur was amorphously dispersed in the carrier,and the interaction existed between drug and carrier. The supersaturation test showed that the order of the ability of polymer to inhibit crystallization of Cur was MF>HF>LF>K30. The dissolution results showed that Cur-K30 amorphous solid dispersion had the highest drug release rate; Cur-K30 and Cur-LF amorphous solid dispersions had a quicker but not stable dissolution rate,and the drug concentration decrease after 4 h; Cur-MF and Cur-HF solid dispersions had a low dissolution,which however increased steadily,attributing to the strong ability of the polymers to inhibit the crystallization of Cur. HPMCAS could inhibit the degradation of Cur better than K30,especially MF and HF. The amorphous solid dispersions of cur significantly enhanced the dissolution of Cur and improved the chemical stability of Cur. This study can provide a basis for the rational selection of the polymer used for Cur solid dispersion.
科研通智能强力驱动
Strongly Powered by AbleSci AI