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A Mathematical Approach to Consider Solid Compressibility in the Compression of Pharmaceutical Powders

机译:在药物粉末压缩中考虑固体压缩性的数学方法

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In-die compression analysis is an effective method for the characterization of powder compressibility. However, physically unreasonable apparent solid fractions above one or apparent in-die porosities below zero are often calculated for higher compression stresses. One important reason for this is the neglect of solid compressibility and hence the assumption of a constant solid density. In this work, the solid compressibility of four pharmaceutical powders with different deformation behaviour is characterized using mercury porosimetry. The derived bulk moduli are applied for the calculation of in-die porosities. The change of in-die porosity due to the consideration of solid compressibility is for instance up to 4% for microcrystalline cellulose at a compression stress of 400 MPa and thus cannot be neglected for the calculation of in-die porosities. However, solid compressibility and further uncertainties from, for example the measured solid density and from the displacement sensors, are difficult or only partially accessible. Therefore, a mathematic term for the calculation of physically reasonable in-die porosities is introduced. This term can be used for the extension of common mathematical models, such as the models of Heckel and of Cooper & Eaton. Additionally, an extended in-die compression function is introduced to precisely describe the entire range of in-die porosity curves and to enable the successful differentiation and quantification of the compression behaviour of the investigated pharmaceutical powders.
机译:模内压缩分析是表征粉末可压缩性的有效方法。但是,对于较高的压缩应力,通常会计算出高于一的物理上不合理的表观固体分数或低于零的表观模内孔隙率。一个重要的原因是忽略了固体可压缩性,因此假设了恒定的固体密度。在这项工作中,使用汞孔隙率法表征了具有不同变形行为的四种药物粉末的固体可压缩性。导出的体积模量用于模内孔隙率的计算。由于考虑了固体可压缩性,模头孔隙度的变化例如对于微晶纤维素在400MPa的压缩应力下高达4%,因此对于模头孔隙度的计算不能忽略。然而,固体可压缩性和来自例如所测量的固体密度和来自位移传感器的进一步的不确定性是困难的或仅部分可获取的。因此,引入了用于计算物理上合理的模内孔隙率的数学术语。该术语可用于扩展常见的数学模型,例如Heckel和Cooper&Eaton的模型。此外,引入了扩展的模内压缩功能,以精确描述模内孔隙率曲线的整个范围,并能够成功地区分和量化所研究药物粉末的压缩行为。

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