Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS)

被引:105
作者
Agarwal, Vikas [2 ]
Siddiqui, Akhtar [1 ]
Ali, Hazem [1 ]
Nazzal, Sami [1 ]
机构
[1] Univ Louisiana Monroe, Coll Pharm, Dept Basic Pharmaceut Sci, Monroe, LA 71209 USA
[2] CIMA LABS INC, Brooklyn Pk, NY USA
关键词
Self-emulsified drug delivery systems; Solid dosage forms; Powder; Rheometry; Dissolution; Powder flow dynamics; BIOAVAILABILITY; CELLULOSE; RELEASE;
D O I
10.1016/j.ijpharm.2008.08.046
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, the dynamics of powder flow upon griseofulvin-self-emulsified drug delivery system(SEDDS) addition to silica and silicates and the effect of these adsorbents on drug release were investigated. SEDDS was adsorbed at SEDDS/adsorbent ratios from 0.25:1 to 3:1 on magnesium aluminum silicate [5 and 80 mu m], calcium silicate [25 mu m], and silicon dioxide [3.6, 20, and 300 mu m]. Powder flow was evaluated using the powder rheometer and compared to angle of repose. Release of drug from a 1: 1 SEDDS/adsorbent powder was determined by dissolution using USP Type 2 apparatus. Powder rheometer profiles indicated that effect of SEDDS on the flow behavior of the adsorbents could be correlated to stepwise or continuous growing behavior as observed in wet granulation process. However, due to their Porous nature, adsorbents exhibited an initial lag phase during which no change in flow was observed. Dissolution of drug from adsorbed-SEDDS was found to be dependent on pore length and nucleation at the lipid/adsorbent interface. Increase in dissolution rate was observed with an increase in surface area and was independent of the chemical nature of the adsorbents. Therefore, in order to manufacture free flowing powder containing liquid SEDDS, special attention should be given to particle size, specific surface area, type and amount of adsorbent. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 52
页数:9
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