Neervannan S, Dias L S, Southard M Z, Stella V J
Department of Pharmaceutical Chemistry, University of Kansas, Lawrence 66045.
Pharm Res. 1994 Sep;11(9):1288-95. doi: 10.1023/a:1018942411536.
A numerical convective-diffusion dissolution model has been extended to describe dissolution of two neutral non-interacting drugs co-compressed in a slab geometry. The model predicted the experimental dissolution rates of naproxen/phenytoin mixtures and hydrocortisone/nitrofurantoin mixtures quite accurately, except for phenytoin in the naproxen/phenytoin mixture at low weight proportions. A non-linear dependence of dissolution rate on weight proportion with a positive deviation from linearity was observed. An increase in flow rate increased the dissolution rate and the cube-root dependency of dissolution rate on the flow rate for a given weight proportion of the component in the slab, as proposed earlier by Shah and Nelson for pure compounds, was also observed here, suggesting that the changes in dissolution profile were caused by changes in surface area only. As expected from the model an increase in particle size of the powders used to make the slab decreased the dissolution rate. This was explained by an increase in the average length of the component resulting in a bigger 'carryover' of material from one section of the component in the slab to the next section of the same component, due to convection, and hence lower flux.
一个数值对流扩散溶解模型已得到扩展,以描述在平板几何形状中共压制的两种中性非相互作用药物的溶解情况。该模型相当准确地预测了萘普生/苯妥英混合物和氢化可的松/呋喃妥因混合物的实验溶解速率,除了在低重量比例下萘普生/苯妥英混合物中的苯妥英。观察到溶解速率对重量比例呈非线性依赖,且偏离线性呈正偏差。流速增加会提高溶解速率,并且对于平板中给定重量比例的组分,溶解速率与流速的立方根依赖性也如沙阿和纳尔逊之前针对纯化合物所提出的那样在此被观察到,这表明溶解曲线的变化仅是由表面积的变化引起的。正如模型所预期的那样,用于制作平板的粉末粒径增加会降低溶解速率。这可以解释为组分平均长度增加,导致由于对流,材料从平板中一个组分的某一段“携带”到同一组分的下一段的量更大,从而通量更低。