Zilberman Meital, Sofer Moran
Department of Biomedical Engineering, Faculty of Engineering, Tel-Aviv University, Tel-Aviv 69978, Israel.
J Biomed Mater Res A. 2007 Mar 1;80(3):679-86. doi: 10.1002/jbm.a.30985.
A mathematical model for predicting bioactive agent release profiles from core/shell fiber structures was developed and studied. These new composite fibers, which combine good mechanical properties with desired protein release profiles, are designed for use in tissue regeneration and other biomedical applications. These fibers are composed of an inner dense polymeric core surrounded by a porous bioresorbable shell, which encapsulates the bioactive agent molecules. The model is based on Fick's second law of diffusion, and on two major assumptions: (a) first-order degradation kinetics of the porous shell, and (b) a nonconstant diffusion coefficient for the bioactive agent, which increases with time because of degradation of the host polymer. Three factors are evaluated and included in this model: a porosity factor, a tortuosity factor, and a polymer concentration factor. Our study indicates that the model correlates well with in vitro release results, exhibiting a mean error of less than 2.2% for most studied cases. In this study, the model was used for predicting protein release profiles from fibers with shells of various initial molecular weights and for predicting the release of proteins with various molecular weights. This new model exhibits a potential for simulating fibrous systems for a wide variety of biomedical applications.
开发并研究了一种用于预测核/壳纤维结构中生物活性剂释放曲线的数学模型。这些新型复合纤维将良好的机械性能与所需的蛋白质释放曲线相结合,设计用于组织再生和其他生物医学应用。这些纤维由内部致密的聚合物核和围绕其的多孔生物可吸收壳组成,壳中封装了生物活性剂分子。该模型基于菲克第二扩散定律,并基于两个主要假设:(a)多孔壳的一级降解动力学,以及(b)生物活性剂的扩散系数随时间变化,这是由于主体聚合物的降解所致。该模型评估并纳入了三个因素:孔隙率因子、曲折度因子和聚合物浓度因子。我们的研究表明,该模型与体外释放结果相关性良好,在大多数研究案例中平均误差小于2.2%。在本研究中,该模型用于预测具有不同初始分子量壳的纤维的蛋白质释放曲线,以及预测不同分子量蛋白质的释放。这种新模型在模拟各种生物医学应用的纤维系统方面具有潜力。