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Numerical Investigation of the Residual Stress Distribution of Flat-Faced and Convexly Curved Tablets Using the Finite Element Method

机译:有限元法数值模拟平板形和凸形曲线片的残余应力分布

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The stress distribution of tablets after compression was simulated using a finite element method, where the powder was defined by the Drucker–Prager cap model. The effect of tablet shape, identified by the surface curvature, on the residual stress distribution was investigated. In flat-faced tablets, weak positive shear stress remained from the top and bottom die walls toward the center of the tablet. In the case of the convexly curved tablet, strong positive shear stress remained on the upper side and in the intermediate part between the die wall and the center of the tablet. In the case of x -axial stress, negative values were observed for all tablets, suggesting that the x -axial force always acts from the die wall toward the center of the tablet. In the flat tablet, negative x -axial stress remained from the upper edge to the center bottom. The x -axial stress distribution differed between the flat and convexly curved tablets. Weak stress remained in the y -axial direction of the flat tablet, whereas an upward force remained at the center of the convexly curved tablet. By employing multiple linear regression analysis, the mechanical properties of the tablets were predicted accurately as functions of their residual stress distribution. However, the multiple linear regression prediction of the dissolution parameters of acetaminophen, used here as a model drug, was limited, suggesting that the dissolution of active ingredients is not a simple process; further investigation is needed to enable accurate predictions of dissolution parameters.
机译:使用有限元方法模拟压片后片剂的应力分布,其中粉末由Drucker-Prager帽模型定义。研究了通过表面曲率确定的片剂形状对残余应力分布的影响。在平面药片中,从顶部和底部模具壁到药片中心的正切应力仍然很弱。在凸形弯曲的片剂的情况下,在模具壁和片剂的中心之间的上侧和中间部分中残留强的正剪切应力。在x轴应力的情况下,所有片剂均观察到负值,这表明x轴力始终从模具壁向片剂中心起作用。在平板电脑中,从上边缘到中心底部保留了负的x轴应力。在平坦和凸形弯曲的片剂之间,x轴应力分布不同。弱应力保持在平板电脑的y轴方向,而向上的力保持在凸形曲线平板电脑的中心。通过采用多元线性回归分析,可以准确预测片剂的机械性能,作为其残余应力分布的函数。但是,这里用作模型药物的对乙酰氨基酚溶出参数的多元线性回归预测是有限的,这表明活性成分的溶出不是一个简单的过程。需要进行进一步的研究以实现溶出参数的准确预测。

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