University of Applied Sciences Northwestern Switzerland, Institute of Pharmaceutical Technology, Gründenstr 40, CH-4132 Muttenz, Switzerland.
Int J Pharm. 2010 May 31;391(1-2):107-14. doi: 10.1016/j.ijpharm.2010.02.027. Epub 2010 Feb 25.
This article focuses on the process analytical technology (PAT) of pharmaceutical dry milling. The first objective is to compare different modes of dynamic image analysis namely, on-line, in-line and at-line for monitoring powder milling. The second objective is to introduce time evolving size and shape analysis (TESSA). Thus, a conical mill was equipped with a dynamic image analysis system which consisted of a xenon flash light and charge-coupled device (CCD) camera. Different pharmaceutical excipients and granulates were chosen as models. The results from the on-line, in-line and the at-line measurement modes showed similar size distributions for the various materials studied, however differences were observed that were mainly attributed to sampling and dispersion. A high correlation of 0.975 (p<0.001) was observed between on-line d(50) and at-line d(50) when compared to 0.917 (p<0.001) between in-line d(50) and at-line d(50). The concept of TESSA was found to be useful in detecting changes in milling conditions including the successful detection of a damaged screen when intentionally introduced in the milling process. This monitoring approach of particle size and shape has potential to reduce product variability, facilitates process development, and ultimately helps in establishing quality by design concept for the manufacture of solid dosage forms.
本文主要关注制药干磨的过程分析技术 (PAT)。第一个目标是比较不同的动态图像分析模式,即在线、在线和离线,以监测粉末磨。第二个目标是介绍时间演变的尺寸和形状分析 (TESSA)。因此,在锥形磨机上配备了一个动态图像分析系统,该系统由氙闪光灯和电荷耦合器件 (CCD) 相机组成。选择了不同的药物赋形剂和颗粒作为模型。在线、在线和离线测量模式的结果表明,研究的各种材料的粒径分布相似,但观察到的差异主要归因于采样和分散。在线 d(50)与离线 d(50)之间的相关性很高,为 0.975(p<0.001),而在线 d(50)与在线 d(50)之间的相关性为 0.917(p<0.001)。发现 TESSA 的概念在检测磨矿条件的变化方面非常有用,包括成功检测到在磨矿过程中故意引入的损坏筛网。这种粒径和形状的监测方法有可能降低产品变异性,促进工艺开发,并最终有助于建立用于制造固体制剂的设计质量概念。