Laboratory of Pharmaceutical Technology, Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
BIOMATH, Department of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000 Ghent, Belgium; Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
Int J Pharm. 2018 Mar 25;539(1-2):1-10. doi: 10.1016/j.ijpharm.2018.01.009. Epub 2018 Jan 31.
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.
最近,提出并评估了一种用于生产单位剂量的连续冷冻干燥工艺。在该概念中,与传统的批量冷冻干燥相比,冷冻步骤进行了修改,因为装满液体制剂的玻璃小瓶在冷却和用冷、无菌和惰性气体(即旋转冷冻)冷冻时绕其纵轴旋转。最后,在整个小瓶壁上实现了一层薄的冷冻产品层。本文的目的有两个:首先,确定了不同小瓶类型下旋转速度与冷冻产品层厚度的顶部和底部之间的相对差异之间的关系。其次,检查了在旋转过程中产生的剪切和离心力的影响,以找出它们是否可能分别导致药物不稳定性和沉淀。机理和实验评估表明,剪切对蛋白质没有影响。计算表明,沉降和扩散速度太低,不会导致产品层不均匀。此外,还进行了全局敏感性分析(GSA)和不确定性分析(UA),以考虑所使用的机理模型的不确定性。