比较计量器和定量盘自动胶囊灌装机的配方要求。

AAPS PharmSci Pub Date : 2002-01-01 DOI:10.1208/ps040317
Pavan K Heda, Kapiamba Muteba, Larry L Augsburger
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引用次数: 0

摘要

本研究的总体目标是为具有代表性的计量器和定量盘胶囊灌装机的配方流动性、润滑性和密实性要求提供 "半定量 "或 "严格 "的定义。为此,我们使用卡尔压缩指数、弹射力和特定压缩力下的断塞力来分别衡量流动性、润滑性和致密性,并针对这些特性开发了模型配方。这些配方分别在 Hofliger-Karg GKF-400 定量圆盘机和 Zanasi LZ-64 定量机上进行封装。每台机器都安装了仪器,用于测量塞子的压缩力和弹射力。对封装过程中的填充重量百分比CV、顶出力、塞子断裂力和配方中标记药物的溶解度进行了评估。使用 f2 指标对溶解曲线进行比较。结果表明:(1) 要在两台机器上成功封装,制剂应满足不同的流动标准;(2) 相对较低的润滑剂水平可能对定量盘机器来说就足够了;(3) 定量器机器需要更高的制剂压实度;(4) 在这些机器类型(根据 FDA 的 SUPAC-IR/MR 制造设备附录,相同类别、不同子类别)之间转移制剂可能具有挑战性。在某些情况下,基于 f2 < 50,在两台机器上以同等压缩力灌装相同制剂的溶出曲线是不同的。总之,本研究结果表明了适合在这两种机器之间转移配方的配方特性范围。
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Comparison of the formulation requirements of dosator and dosing disc automatic capsule filling machines.

The overall objective of this study was to provide 'semi-quantitative' or 'rigorous' definitions of the fluidity, lubricity and compactibility requirements of formulation for representative dosator and dosing disc capsule filling machines. To that end, model formulations were developed for those properties using Carr's compressibility index, ejection force, and plug breaking force at a specified compression force to gauge fluidity, lubricity, and compactibility, respectively. These formulations were each encapsulated on an Hofliger-Karg GKF-400 dosing disc machine and a Zanasi LZ-64 dosator machine. Each machine was instrumented to measure plug compression and ejection forces. The encapsulation process was evaluated for %CV of fill-weight, ejection force, plug breaking force and the dissolution of marker drugs incorporated in the formulations. The f2 metric was used to compare dissolution profiles. The results suggest: (1) formulations should meet different flow criteria for successful encapsulation on the two machines, (2) a relatively lower level of lubricant may be sufficient for the dosing disc machine, (3) a higher degree of formulation compactibility is needed for the dosator machine, and (4) transferring formulations between these machine types (same class, different subclass per FDA's SUPAC-IR/MR Manufacturing Equipment Addendum) could be challenging. In certain cases dissolution profiles for the same formulation filled on the two machines with equivalent compression force were different based on f2 < 50. Overall, the results of this study suggest a range of formulation characteristics appropriate for transferring formulations between these two types of machines.

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