首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Particle sizing measurements in pharmaceutical applications: Comparison of in-process methods versus off-line methods
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Particle sizing measurements in pharmaceutical applications: Comparison of in-process methods versus off-line methods

机译:制药应用中的颗粒尺寸测量:在线方法与离线方法的比较

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摘要

It has been previously described that when a sample's particle size is determined using different sizing techniques, the results can differ considerably. The purpose of this study was to review several in-process techniques for particle size determination (Spatial Filtering Velocimetry, Focused Beam Reflectance Measurements, Photometric Stereo Imaging, and the Eyecon? technology) and compare them to well-known and widespread off-line reference methods (laser diffraction and sieve analysis). To start with, a theoretical explanation of the working mechanism behind each sizing technique is presented, and a comparison between them is established. Secondly, six batches of granules and pellets (i.e., spherical particles) having different sizes were measured using these techniques. The obtained size distributions and related D10, D50, and D90 values were compared using the laser diffraction wet dispersion method as reference technique. As expected, each technique provided different size distributions with different D values. These dissimilarities were examined and explained considering the measurement principles behind each sizing technique. The particle property measured by each particle size analyzer (particle size or chord length) and how it is measured as well as the way in which size information is derived and calculated from this measured property and how results are presented (e.g., volume or mass distributions) are essential for the interpretation of the particle size data.
机译:先前已经描述过,当使用不同的上浆技术确定样品的粒径时,结果可能会大大不同。这项研究的目的是回顾几种确定粒径的过程中技术(空间滤波测速,聚焦光束反射率测量,光度立体成像和Eyecon?技术),并将它们与众所周知的广泛离线参考进行比较方法(激光衍射和筛分分析)。首先,对每种上浆技术背后的工作机理进行了理论解释,并进行了比较。其次,使用这些技术测量了六批具有不同尺寸的颗粒和丸剂(即球形颗粒)。使用激光衍射湿分散法作为参考技术比较获得的尺寸分布和相关的D10,D50和D90值。不出所料,每种技术都提供了具有不同D值的不同大小分布。考虑了每种上浆技术背后的测量原理,对这些差异进行了检查和解释。每个粒度分析仪测量的颗粒特性(粒度或弦长),以及如何测量以及从该测量特性导出和计算尺寸信息的方式以及如何表示结果(例如,体积或质量分布) )对于解释粒度数据至关重要。

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