| Literature DB >> 29366945 |
Joris Lammens1, Séverine Thérèse F C Mortier2, Laurens De Meyer3, Brecht Vanbillemont4, Pieter-Jan Van Bockstal5, Simon Van Herck6, Jos Corver7, Ingmar Nopens8, Valérie Vanhoorne9, Bruno G De Geest10, Thomas De Beer11, Chris Vervaet12.
Abstract
Recently, a continuous freeze-drying process for the production of unit doses was presented and evaluated. In this concept, the freezing step is modified compared to traditional batch freeze-drying, as glass vials filled with a liquid formulation, are rotated around their longitudinal axis while cooled and frozen with a cold, sterile and inert gas (i.e. spin freezing). Finally, a thin frozen product layer spread over the entire vial wall is achieved. The aim of this paper is twofold: firstly, the relation between the rotation velocity and the relative difference between top and bottom of the frozen product layer thickness was determined for different vial types. Secondly, the impact of shear and centrifugal forces generated during spinning was examined, to find out whether they might cause pharmaceutical instability and sedimentation, respectively. Mechanistic and experimental evaluation showed that shear has no effect on proteins. Calculations showed that the sedimentation and diffusion velocity is too low to cause inhomogeneity in the product layer. In addition, Global Sensitivity Analysis (GSA) and Uncertainty Analysis (UA) were performed in order to account for the uncertainty of the used mechanistic model.Keywords: Diffusion; Freeze-drying; Global sensitivity analysis; Sedimentation; Shear; Uncertainty analysis
Mesh:
Year: 2018 PMID: 29366945 DOI: 10.1016/j.ijpharm.2018.01.009
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875