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

Int J Pharm

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

Published: June 2023

AI Article Synopsis

  • Continuous spin freeze-drying allows for the integration of process analytical technologies (PAT) to enhance control over the freeze-drying process at the vial level.
  • Two key methods were developed: one to individually control the freezing phase's cooling and freezing rates, and another to manage the drying phase by adjusting vial temperature and monitoring moisture content.
  • This control led to consistently structured products, homogeneous drying times across samples, and accurate in-line moisture monitoring to optimize the duration of the secondary drying phase.

Article 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.

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Source
http://dx.doi.org/10.1016/j.ijpharm.2023.123062DOI Listing

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