PHYSICAL MODEL FOR RELEASE OF DRUG FROM GELFORMING SUSTAINED-RELEASE PREPARATIONS

被引:31
作者
BAMBA, M [1 ]
PUISIEUX, F [1 ]
MARTY, JP [1 ]
CARSTENSEN, JT [1 ]
机构
[1] UNIV WISCONSIN,SCH PHARM,MADISON,WI 53706
关键词
D O I
10.1016/0378-5173(79)90069-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Certain sustained release preparations contain a substance which, when exposed to an aqueous medium, forms a gel. Liquid will continue to penetrate the gel layer with time (θ) and the release of drug is both a function of liquid penetration rates (α) and diffusion of drug through the gelled layer (with a permeation coefficient of II). The thickness of the layer will be a function of time, because as liquid penetrates, more gel is formed. Development of this model leads to a third-power equation for the amount of drug released (m) as a function of time: m = aθ3 + bθ2 + cθ; the coefficients a, b and c contain an integral: f{hook}10 exp[(-π/α)(1/u)du which is evaluated graphically and found equal to 0.93 exp[-2.6π/α]. The data by Bamba et al. (1979) were used to demonstrate that the fit of experimental data to the third-power equation is a good as or superior to conventional plotting techniques. © 1979.
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页码:87 / 92
页数:6
相关论文
共 3 条
  • [1] RELEASE MECHANISMS IN GELFORMING SUSTAINED-RELEASE PREPARATIONS
    BAMBA, M
    PUISIEUX, F
    MARTY, JP
    CARSTENSEN, JT
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1979, 2 (5-6) : 307 - 315
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  • [3] CARSTENSEN JT, 1978, J PHARM SCI, V67, P48, DOI 10.1002/jps.2600670113