Stay Matthew S, Xu Jing, Randolph Theodore W, Barocas Victor H
Graduate Program in Scientific Computation, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Pharm Res. 2003 Jan;20(1):96-102. doi: 10.1023/a:1022207026982.
Biodistribution of drugs in the eye is central to the efficacy of pharmaceutical ocular therapies. Of particular interest to us is the effect of intravitreal transport on distribution of controlled-released drugs within the vitreous.
A computer model was developed to describe the three-dimensional convective-diffusive transport of drug released from an intravitreal controlled release source. Unlike previous studies, this work includes flow of aqueous from the anterior to the posterior of the vitreous. The release profile was based on in vitro release of gentamicin from poly(L-lactic acid) microspheres into vitreous.
For small drugs, convection plays a small role, but for large (slower diffusing) drugs, convection becomes more important. For the cases studied, the predicted ratio of drug reaching the retina to drug cleared by the aqueous humor was 2.4 for a small molecule but 13 for a large molecule. Transport in neonatal mouse eye, in contrast, was dominated by diffusion, and the ratio decreased to 0.39.
The interaction among convection, diffusion, and geometry causes significant differences in biodistribution between large and small molecules or across species. These differences should be considered in the design of delivery strategies or animal studies.
药物在眼内的生物分布对于眼部药物治疗的疗效至关重要。我们特别感兴趣的是玻璃体内转运对玻璃体内控释药物分布的影响。
建立了一个计算机模型来描述从玻璃体内控释源释放的药物的三维对流扩散转运。与以往的研究不同,这项工作包括房水从玻璃体前部到后部的流动。释放曲线基于庆大霉素从聚(L-乳酸)微球向玻璃体的体外释放。
对于小分子药物,对流起的作用较小,但对于大分子(扩散较慢)药物,对流变得更为重要。在所研究的案例中,预测到达视网膜的药物与被房水清除的药物的比例,小分子为2.4,大分子为13。相比之下,新生小鼠眼内的转运以扩散为主,该比例降至0.39。
对流、扩散和几何形状之间的相互作用导致大分子和小分子之间或不同物种之间的生物分布存在显著差异。在设计给药策略或进行动物研究时应考虑这些差异。