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Effect of Process Variables on the Drucker–Prager Cap Model and Residual Stress Distribution of Tablets Estimated by the Finite Element Method

机译:过程变量对Drucker-Prager Cap模型和片剂残余应力分布的有限元估计影响

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A multivariate statistical technique was applied to clarify the causal correlation between variables in the manufacturing process and the residual stress distribution of tablets. Theophylline tablets were prepared according to a Box–Behnken design using the wet granulation method. Water amounts ( X 1), kneading time ( X 2), lubricant-mixing time ( X 3), and compression force ( X 4) were selected as design variables. The Drucker–Prager cap (DPC) model was selected as the method for modeling the mechanical behavior of pharmaceutical powders. Simulation parameters, such as Young’s modulus, Poisson rate, internal friction angle, plastic deformation parameters, and initial density of the powder, were measured. Multiple regression analysis demonstrated that the simulation parameters were significantly affected by process variables. The constructed DPC models were fed into the analysis using the finite element method (FEM), and the mechanical behavior of pharmaceutical powders during the tableting process was analyzed using the FEM. The results of this analysis revealed that the residual stress distribution of tablets increased with increasing X 4. Moreover, an interaction between X 2 and X 3 also had an effect on shear and the x -axial residual stress of tablets. Bayesian network analysis revealed causal relationships between the process variables, simulation parameters, residual stress distribution, and pharmaceutical responses of tablets. These results demonstrated the potential of the FEM as a tool to help improve our understanding of the residual stress of tablets and to optimize process variables, which not only affect tablet characteristics, but also are risks of causing tableting problems.
机译:应用了多元统计技术来阐明片剂制造过程中变量与残余应力分布之间的因果关系。根据Box-Behnken设计,使用湿法制粒制备茶碱片。水量(X 1 ),捏合时间(X 2 ),润滑剂混合时间(X 3 )和压缩力(X < sub> 4 )作为设计变量。选择了Drucker-Prager瓶盖(DPC)模型作为对药物粉末力学行为进行建模的方法。测量了诸如杨氏模量,泊松比,内摩擦角,塑性变形参数和粉末初始密度等模拟参数。多元回归分析表明,仿真参数受到过程变量的显着影响。使用有限元方法(FEM)将构建的DPC模型输入到分析中,并使用FEM分析压片过程中药物粉末的力学行为。分析结果表明,片剂的残余应力分布随X 4 的增加而增加。此外,X 2 和X 3 之间的相互作用也对片剂的剪切力和x轴残余应力有影响。贝叶斯网络分析揭示了过程变量,模拟参数,残余应力分布和片剂的药物反应之间的因果关系。这些结果证明了有限元法作为一种工具的潜力,可以帮助我们更好地理解片剂的残余应力并优化工艺变量,这些变量不仅影响片剂的特性,而且还存在引起片剂问题的风险。

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