通过直接压制连续生产固体制剂的压片机控制中的变异和风险分析

Qinglin Su, Yasasvi Bommireddy, Marcial Gonzalez, Gintaras V Reklaitis, Zoltan K Nagy
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引用次数: 0

摘要

连续旋转式压片机是一个多工序过程,有许多冲压站并行运行,其中每个冲压站都要经过以下步骤:模具填充和计量、预压实、主压实、片剂顶出以及从下部冲压站取片。冲压工位内部或压片机各工位之间的工艺不确定性或干扰是导致最终产品质量属性(如硬度、重量等)变化的主要原因,进而给固体制剂的制药连续生产中的实时释放带来了挑战。本研究对普渡大学的直接压片生产线进行了调查,并使用 Natoli BLP-16 压片机对粉末可压缩性、系统动态和变化以及对过程控制开发的交互影响进行了表征。研究发现,由对乙酰氨基酚(原料药)、Avicel 微晶纤维素 PH-200(赋形剂)和二氧化硅(润滑剂)混合制成的片剂的可压缩性在很大程度上与压片速度无关。相比之下,灌装深度或定量水平、转塔速度、进料架速度和压紧力相互影响,并对模头灌装工艺和最终产品质量属性产生重大影响。因此,工艺控制结构的设计在减少工艺和产品质量变化方面发挥着重要作用。我们提出并评估了一种分级式三级控制设计,包括 0 级纳托利内置控制、用于片剂重量和生产率控制的 1 级解耦比例积分微分级联控制回路,以及 2 级高级模型预测控制。此外,还研究了连续稳态运行期间的工艺变化,如粉末体积密度变化。最后,简要讨论并总结了工艺动态变化对产品质量控制影响的风险分析。
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Variation and Risk Analysis in Tablet Press Control for Continuous Manufacturing of Solid Dosage via Direct Compaction.

A continuous rotary tablet press is a multi-stage process with many punch stations running in parallel, in which each punch undergoes the following steps: die filling and metering, pre-compaction, main-compaction, tablet ejection, and tablet take-off from lower punch. Process uncertainties or disturbances within a punch station or among stations in the tablet press are a major source of variation in final product quality attributes, e.g., hardness, weight, etc., which in turn imposes challenges for the real-time release in pharmaceutical continuous manufacturing of solid dosage. In this study, the direct compression line at Purdue University was investigated and a Natoli BLP-16 tablet press was used to characterize powder compressibility, system dynamics and variation, as well as the interaction effects on process control development. The compressibility of tablets made from a blend of Acetaminophen (API), Avicel Microcrystalline Cellulose PH-200 (excipient), and SiO2 (lubricant) was found to be largely independent of tableting speed. By contrast, filling depth or dosing level, turret speed, feed-frame speed, and compression force were interacting and significantly affected the die-filling process and the final product quality attributes. Thus, the design of the process control structure plays an important role in reducing process and product quality variations. A hierarchical three-level control design was proposed and evaluated, consisting of Level 0 Natoli built-in control, Level 1 decoupled Proportional Integral Derivative (PID) cascaded control loops for tablet weight and production rate control, and Level 2 advanced model predictive control. Process variations, e.g., in powder bulk density changes, during continuous steady-state operation were also investigated. Finally, a risk analysis of the effects of the process dynamics on variation on the product quality control was briefly discussed and summarized.

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