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一种考虑药物粉末压缩过程中固体可压缩性的数学方法。

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

作者信息

Wünsch Isabell, Finke Jan Henrik, John Edgar, Juhnke Michael, Kwade Arno

机构信息

Institute for Particle Technology, Technische Universität Braunschweig, Volkmaroder Straße 5, Braunschweig 38104, Germany.

Center of Pharmaceutical Engineering (PVZ), Technische Universität Braunschweig, Braunschweig 38106, Germany.

出版信息

Pharmaceutics. 2019 Mar 15;11(3):121. doi: 10.3390/pharmaceutics11030121.

Abstract

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.

摘要

模内压缩分析是表征粉末可压缩性的有效方法。然而,对于较高的压缩应力,常常会计算出高于1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。造成这种情况的一个重要原因是忽略了固体的可压缩性,因此假设固体密度恒定。在这项工作中,使用压汞法表征了四种具有不同变形行为的药用粉末的固体可压缩性。导出的体积模量用于计算模内孔隙率。例如,在400 MPa的压缩应力下,考虑固体可压缩性导致的模内孔隙率变化对于微晶纤维素高达4%,因此在计算模内孔隙率时不能忽略。然而,固体可压缩性以及例如测量的固体密度和位移传感器带来的进一步不确定性很难获取或只能部分获取。因此,引入了一个用于计算物理上合理的模内孔隙率的数学项。该项可用于扩展常见的数学模型,如赫克尔模型以及库珀和伊顿模型。此外,引入了一个扩展的模内压缩函数,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用粉末的压缩行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bb/6470607/fe1d1ad29c47/pharmaceutics-11-00121-g001.jpg

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