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Geometric Modeling and Parametric Characterization for Virtual Design of Pharmaceutical Tablets

机译:药物片剂虚拟设计的几何建模和参数表征

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The mechanisms involved for compaction of pharmaceutical powders have become a crucial step in the development cycle for tablet design. Compressibility and compactibility are two important properties which define the ability of loose powder to transform into a compact. The compacted powder, also known as tablet, needs to be strong enough in order to handle different types of stress due to packaging and loading conditions. This work presents a technique for designing solid tablets based on the use of Partial Differential Equations (PDEs). The shape and size of the generated tablet can be changed by exploiting the analytic expressions relating the coefficients associated with the PDE method. This work also has simulated the compressibility of pharmaceutical powders by utilizing deformation models found in literature. The results are analyzed using the Heckel model. Finally, the automatic design optimization is performed by combining the PDE method and a standard method for numerical optimization for obtaining optimal design of tablets with maximum tensile strength. The results show that the PDE method is able to represent the physical changes of the deformed tablet.
机译:压制药物粉末的机制已成为片剂设计开发周期中的关键步骤。可压缩性和可压实性是两个重要的属性,它们定义了散装粉末转变为压块的能力。压实的粉末(也称为片剂)需要足够坚固,以应对由于包装和装载条件而产生的不同类型的压力。这项工作提出了一种基于偏微分方程(PDE)的设计固体片剂的技术。可以通过利用与PDE方法相关的系数相关的解析表达式来更改生成的药片的形状和大小。这项工作还利用文献中发现的变形模型模拟了药物粉末的可压缩性。使用Heckel模型分析结果。最后,通过将PDE方法和标准方法进行数值优化相结合来进行自动设计优化,以获得具有最大抗拉强度的片剂的最佳设计。结果表明,PDE方法能够代表变形片剂的物理变化。

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