硬脂酸镁
压片
润滑油
乳糖
无水的
材料科学
润滑
工艺工程
造粒
化学工程
复合材料
色谱法
剂型
化学
食品科学
有机化学
工程类
作者
Gerald A. Hebbink,Pauline H.M. Janssen,Jurjen H. Kok,Lorenzo Menarini,Federica Giatti,Caterina Funaro,S. Consoli,Bastiaan H.J. Dickhoff
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-11-03
卷期号:15 (11): 2575-2575
被引量:1
标识
DOI:10.3390/pharmaceutics15112575
摘要
Modern pharmaceutical manufacturing based on Quality by Design and digitalisation is revolutionising the pharmaceutical industry. Continuous processes are promoted as they increase efficiency and improve quality control. Compared to batch blending, continuous blending is easier to scale and provides advantages for achieving blend homogeneity. One potential challenge of continuous blending is the risk of over-lubrication. In this study, blending homogeneity and lubricant sensitivity are investigated for both batch and continuous processes. Given their distinct chemical structures and morphologies, anhydrous lactose and granulated lactose are expected to exhibit varying sensitivities to changes in process settings across both technologies. The findings suggest that both lactose grades provide highly stable blends that can be safely utilised in both batch and continuous modes. Optimisation should focus on process variables, such as the quality of loss-in-weight feeders used for dosing low doses of ingredients. The most significant process parameter for lubricant sensitivity was the type of lactose used. Anhydrous lactose produced harder tablets than the more porous granulated lactose but was more sensitive to lubrication at the same settings. The magnesium stearate content and its interaction with the type of lactose are also critical factors, with magnesium stearate having a counterproductive impact on tabletability.
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