The Preparation of Ternary Solid Dispersions of an Herbal Drug via Spray Drying of Liquid Feed

被引:44
作者
Araujo, R. R. [1 ]
Teixeira, C. C. C. [1 ]
Freitas, L. A. P. [1 ]
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bioavailability; Curcumin; Dissolution; Hard gelatin capsules; Solubility; MALTODEXTRIN ADDITION; DEHUMIDIFIED AIR; DRIED PROPOLIS; TOMATO PULP; MICROENCAPSULATION; EXTRACT;
D O I
10.1080/07373931003648540
中图分类号
TQ [化学工业];
学科分类号
081705 [工业催化];
摘要
The present study aimed the preparation and characterization of ternary solid dispersions by direct spray drying of a liquid suspension containing curcumin, a solubility enhancer and a drying aid. The experiments followed a Box-Behnken design in order to evaluate the influence of temperature, ratio of curcumin: lipidic carrier, and the collodial silicon dioxide content on the characteristics of the microparticulated solid dispersions. The angle of repose, Hausner factor, Carr index, water activity, and solubility were used to characterize solid dispersions. The results show that water activity, Hausner factor, and Carr index varied in an acceptable range for pharmaceutical purposes. The condition that maximizes solubility was determined using an exploratory design based on a surface response analysis and allowed a 3200-fold increase in curcumin solubility. Ternary solid dispersion showed a 90% curcumin release after 10min during a dissolution test. The results show that the spray drying of a liquid feed is an attractive and promising alternative to obtain enhanced solubility drug ternary solid dispersions.
引用
收藏
页码:412 / 421
页数:10
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