Dipartimento di Chimica, Materiali e Ingegneria Chimica Giulio Natta, Politecnico di Milano, Via Mancinelli 7, 20131 Milano, Italy.
Int J Pharm. 2012 Jun 15;429(1-2):148-57. doi: 10.1016/j.ijpharm.2012.03.024. Epub 2012 Mar 22.
This work is focused on the development of a transient 1-dimension model to describe drug release from a bioresorbable suture thread in a living tissue and the pharmacologic behavior of the active substance being delivered from the device into the tissue. The model is based on fundamental conservation laws, represented by mass balances, being the thread degradation described through population balances and involving detailed hydrolysis kinetics. Monomer, water and drug diffusion are assumed as Fickian, and the increasing of diffusion coefficient is expressed with the "free volume" theory. Drug behavior in tissue is described with a "diffusion and reaction" approach. The model leads to a system of partial differential equations solved by applying the method of lines and then numerically integrated. Simulations allowed to estimate release dynamics and drug behavior in tissue and to obtain spatial and temporal profiles of drug in tissue. Moreover, phase diagrams, which show drug effect in time and space, are here introduced for the first time.
这项工作专注于开发一个瞬态一维模型,以描述可生物吸收缝线在活组织中的药物释放以及从装置递送至组织中的活性物质的药理行为。该模型基于基本守恒定律,由质量平衡表示,缝线降解通过群体平衡描述,并涉及详细的水解动力学。单体、水和药物扩散被假定为菲克定律,扩散系数的增加用“自由体积”理论表示。组织中的药物行为用“扩散和反应”方法来描述。该模型导致一个偏微分方程组,通过应用线方法求解,然后进行数值积分。模拟允许估计释放动力学和药物在组织中的行为,并获得组织中药物的时空分布。此外,首次引入了显示药物在时间和空间上的效果的相图。