Early prediction of tablet defects during pan coating

IF 5.1 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Joona Sorjonen , Luis Martin de Juan , Pirjo Tajarobi , Håkan Wikström , Jarkko Ketolainen
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引用次数: 0

Abstract

The appearance of a tablet is a critical quality attribute that can be directly evaluated by patients. During tablet manufacturing, mechanical stress may lead to visual defects, such as edge chipping, the prediction of which remains a major challenge, particularly during technology transfer or scale-up processes. This study aimed to evaluate whether the number and severity of defects could be predicted under two mechanical stress environments: pan coating and friabilator testing.
A breakage model was calibrated using drop tests with two placebo formulations: mannitol:microcrystalline cellulose (7:3) and microcrystalline cellulose:anhydrous dibasic calcium phosphate (7:3), both at target tensile strengths of 1.5–2.5 MPa. Discrete element method (DEM) simulations were used to estimate the collision velocities and frequencies in the coating pan, enabling defect prediction using the breakage model. One verification run was performed using the mannitol:MCC 7:3 formulation at 2.0 MPa, which was also used to predict the tablet appearance in the friabilator.
The model accurately predicted the severity of defects (Classes I–III, where I is the least and III the most severe defect) in the coating trial but underestimated the number of Class I defects. The numerical predictions made by the model are exponentially affected by inaccuracies in the calibration of model parameters, particularly for small damage. Visual differences between tablets with equal mass loss in the friabilator and pan coater also suggest that wear from low-force collisions contributed to damage during the coating process. In contrast, the number of appearance defects was overpredicted in the friabilator, highlighting the model’s limitations in systems with frequent collisions. Overall, with careful calibration and under conditions with few defect-causing events, the model can provide useful guidance for defect prediction.

Abstract Image

涂布过程中片剂缺陷的早期预测。
片剂的外观是一项关键的质量属性,可由患者直接评价。在片剂制造过程中,机械应力可能导致视觉缺陷,如边缘剥落,这仍然是一个主要的挑战,特别是在技术转移或放大过程中。本研究旨在评估在两种机械应力环境下:pan涂层和脆性试验是否可以预测缺陷的数量和严重程度。使用两种安慰剂配方:甘露醇:微晶纤维素(7:3)和微晶纤维素:无水二碱磷酸钙(7:3),在1.5-2.5 MPa的目标抗拉强度下,使用跌落试验校准破损模型。采用离散元法(DEM)进行模拟,估计了涂层盘内的碰撞速度和频率,实现了基于破损模型的缺陷预测。在2.0 MPa下,以甘露醇:MCC 7:3的配方进行验证,并用于预测片剂在破碎机中的外观。该模型准确地预测了涂层试验中缺陷的严重程度(I-III类,其中I是最小的,III是最严重的缺陷),但低估了I类缺陷的数量。模型所作的数值预测受到模型参数校准误差的指数影响,特别是对于小损伤。在破碎机和涂覆机中损失相同质量的片剂之间的视觉差异也表明,在涂覆过程中,低力碰撞造成的磨损造成了损伤。相比之下,在易碎器中,外观缺陷的数量被高估了,这突出了模型在频繁碰撞系统中的局限性。总的来说,通过仔细的校准和在很少引起缺陷事件的条件下,该模型可以为缺陷预测提供有用的指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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