Institute of Pharmaceutical Technology, Faculty of Pharmacy, Belgrade, Serbia.
J Pharm Pharmacol. 2009 Nov;61(11):1449-56. doi: 10.1211/jpp/61.11.0003.
The main objective of this study was to develop a mathematical model for the characterization of diclofenac sodium diffusion from polyethylene oxide (PEO) matrices. A model was developed on the basis of the diffusion theory accounting for the characteristics of the polymer: swelling with subsequent dissolution in water. The concentration-dependent diffusion of drug and water was taken into account. Experimental data were analysed using a computer software program as an aid for solving partial differential equations.
Six formulations of matrix tablets with different drug-excipient ratios were prepared using low-molecular-weight PEO as a matrix-forming material. For obtaining drug release data, dissolution studies were performed and water uptake by pure PEO matrices was studied as well.
A good agreement of the developed model with experimental results was demonstrated. Some anomalies in drug diffusion were observed and their origin was questioned. Changes in the parameters characterizing the process of diffusion are attributed to glassy-rubbery polymer transitions. Additional interpretation of this phenomenon on the basis of percolation theory is also provided.
The obtained model has the ability to predict the required characteristics of matrices for desired drug release. The composition of batches with undesirable release properties can be predetermined and avoided in manufacturing.
本研究的主要目的是建立一个从聚乙烯氧化物(PEO)基质中扩散双氯芬酸钠的数学模型。该模型是基于扩散理论建立的,考虑了聚合物的特性:溶胀随后在水中溶解。考虑了药物和水的浓度依赖性扩散。使用计算机软件程序分析实验数据,以帮助求解偏微分方程。
使用低分子量 PEO 作为基质形成材料,制备了具有不同药物-赋形剂比的六种基质片剂配方。为了获得药物释放数据,还进行了溶解研究,并研究了纯 PEO 基质的吸水率。
该模型与实验结果具有良好的一致性。观察到药物扩散中的一些异常现象,并对其来源提出了质疑。描述扩散过程的参数的变化归因于玻璃态-橡胶态聚合物转变。还基于渗流理论对该现象提供了进一步的解释。
所获得的模型具有预测所需药物释放特性的基质的能力。可以预先确定具有不理想释放特性的批次的组成,并在制造过程中避免。