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Comparison of the formulation requirements of dosator and dosing disc automatic capsule filling machines

机译:计量器和计量盘自动胶囊填充机的配方要求比较

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摘要

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.
机译:这项研究的总体目标是为代表性定量给料机和定量盘式胶囊填充机的配方的流动性,润滑性和致密性要求提供“半定量”或“严格”定义。为此,使用Carr的可压缩指数,弹射力和在指定压缩力下的塞子破坏力来开发这些特性的模型公式,以分别衡量流动性,润滑性和可压实性。将这些制剂分别封装在Hofliger-Karg GKF-400配料盘式机器和Zanasi LZ-64配料器上。每台机器都经过仪器测量,以测量塞子的压缩和顶出力。评估包囊过程中填充重量的%CV,喷射力,塞子破坏力和制剂中掺入的标记药物的溶出度。 f2指标用于比较溶出度曲线。结果表明:(1)制剂应满足不同的流动标准,才能成功封装在两台机器上;(2)剂量相对较低的润滑剂可能足以满足计量圆盘机器的需求;(3)需要更高程度的制剂致密性(4)在这些机器类型(FDA的SUPAC-IR / MR制造设备附录中相同类别,不同子类别)之间转移配方可能具有挑战性。在某些情况下,以相等的压缩力在两台机器上填充的相同配方的溶出曲线基于f2 <50而不同。总的来说,这项研究的结果表明了一系列适合在这两种机器之间转移配方的配方特性。

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