Centre for Visual Computing, University of Bradford, Bradford BD7 1DP, UK.
Int J Pharm. 2011 Feb 28;405(1-2):113-21. doi: 10.1016/j.ijpharm.2010.12.006. Epub 2010 Dec 9.
The mechanisms involved for compaction of pharmaceutical powders have become a crucial step in the development cycle for robust tablet design with required properties. Compressibility of pharmaceutical materials is measured by a force-displacement relationship which is commonly analysed using a well known method, the Heckel model. This model requires the true density and compacted powder mass value to determine the powder mean yield pressure. In this paper, we present a technique for shape modelling of pharmaceutical tablets based on the use of partial differential equations (PDEs). This work also presents an extended formulation of the PDE method to a higher dimensional space by increasing the number of parameters responsible for describing the surface in order to generate a solid tablet. Furthermore, the volume and the surface area of the parametric cylindrical tablet have been estimated numerically. Finally, the solution of the axisymmetric boundary value problem for a finite cylinder subject to a uniform axial load has been utilised in order to model the displacement components of a compressed PDE-based representation of a tablet. The Heckel plot obtained from the developed model shows that the model is capable of predicting the compaction behaviour of pharmaceutical materials since it fits the experimental data accurately.
用于药物粉末压实的机制已成为具有所需性质的坚固片剂设计的开发周期中的关键步骤。药物材料的可压缩性通过力-位移关系来测量,通常使用一种著名的方法,即 Heckel 模型来分析该关系。该模型需要真实密度和压实粉末质量值来确定粉末平均屈服压力。在本文中,我们提出了一种基于偏微分方程 (PDE) 的药物片剂形状建模技术。这项工作还通过增加负责描述表面的参数数量,将 PDE 方法的扩展公式扩展到更高维空间,以生成实心片剂。此外,还对参数圆柱形片剂的体积和表面积进行了数值估计。最后,利用轴对称边界值问题的解对受均匀轴向载荷作用的有限圆柱进行建模,以模拟基于 PDE 的片剂压缩表示的位移分量。从开发的模型中获得的 Heckel 图表明,该模型能够准确地预测药物材料的压缩行为,因为它准确地拟合了实验数据。