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基于 PAT 的在线控制系统在连续旋转冷冻干燥过程中的评估。

Evaluation of a PAT-based in-line control system for a continuous spin freeze-drying process.

机构信息

Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, 9000 Ghent, Belgium.

Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, 9000 Ghent, Belgium.

出版信息

Int J Pharm. 2023 Jun 25;641:123062. doi: 10.1016/j.ijpharm.2023.123062. Epub 2023 May 18.

Abstract

Continuous spin freeze-drying provides a range of opportunities regarding the implementation of several in-line process analytical technologies (PAT) to control and optimize the freeze-drying process at the individual vial level. In this work, two methods were developed to (1) control the freezing phase by separately controlling the cooling and freezing rate and (2) control the drying phase by controlling the vial temperature (and hence the product temperature) to setpoint values and monitoring the residual moisture content. During the freezing phase, the vial temperature closely followed the decreasing setpoint temperature during the cooling phases, and the crystallization phase was reproducibly controlled by regulating the freezing rate. During both primary and secondary drying, vial temperature could be maintained on the setpoint temperature which resulted in an elegant cake structure after every run. By being able to accurately control the freezing rate and the vial temperature, a homogeneous drying time (SD = 0.07-0.09 h) between replicates was obtained. Applying a higher freezing rate significantly increased primary drying time. On the other hand, fast freezing rates increased the desorption rate. Finally, the residual moisture of the freeze-dried formulation could be monitored in-line with a high accuracy providing insight on the required length of the secondary drying phase.

摘要

连续旋转冻干为多种在线过程分析技术(PAT)的实施提供了一系列机会,可在每个小瓶级别控制和优化冻干过程。在这项工作中,开发了两种方法来(1)通过分别控制冷却和冻结速率来控制冷冻阶段,(2)通过控制小瓶温度(从而控制产品温度)来设定点值并监测残余水分含量来控制干燥阶段。在冷冻阶段,小瓶温度在冷却阶段随设定点温度的降低而紧密跟踪,并且通过调节冻结速率可以重复控制结晶阶段。在主干燥和次干燥期间,小瓶温度都可以保持在设定点温度,从而在每次运行后都得到了结构良好的干块。通过能够准确地控制冻结速率和小瓶温度,可以在重复之间获得均匀的干燥时间(SD = 0.07-0.09 h)。采用更高的冻结速率会显著增加主干燥时间。另一方面,快速冻结速率会增加解吸速率。最后,可以在线以高精度监测冻干配方的残余水分,从而深入了解二次干燥阶段的所需长度。

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