Research Center Pharmaceutical Engineering, Graz, Austria; Institute of Biotechnology and Biochemical Engineering, Graz University of Technology, Graz, Austria.
J Pharm Sci. 2014 Feb;103(2):417-26. doi: 10.1002/jps.23814. Epub 2013 Dec 13.
A 300-mL stainless steel freeze container was constructed to enable QbD (Quality by Design)-compliant investigations and the optimization of freezing and thawing (F/T) processes of protein pharmaceuticals at moderate volumes. A characterization of the freezing performance was conducted with respect to freezing kinetics, temperature profiling, cryoconcentration, and stability of the frozen protein. Computational fluid dynamic (CFD) simulations of temperature and phase transition were established to facilitate process scaling and process analytics as well as customization of future freeze containers. Protein cryoconcentration was determined from ice-core samples using bovine serum albumin. Activity, aggregation, and structural perturbation were studied in frozen rabbit muscle l-lactic dehydrogenase (LDH) solution. CFD simulations provided good qualitative and quantitative agreement with highly resolved experimental measurements of temperature and phase transition, allowing also the estimation of spatial cryoconcentration patterns. LDH exhibited stability against freezing in the laboratory-scale system, suggesting a protective effect of cryoconcentration at certain conditions. The combination of the laboratory-scale freeze container with accurate CFD modeling will allow deeper investigations of F/T processes at advanced scale and thus represents an important step towards a better process understanding.
构建了一个 300 毫升的不锈钢冷冻容器,以实现符合 QbD(质量源于设计)要求的调查,并优化蛋白质药物在中等体积下的冷冻和融化(F/T)过程。对冷冻性能进行了特征描述,包括冷冻动力学、温度分布、冰晶浓缩和冷冻蛋白质的稳定性。建立了计算流体动力学(CFD)模拟温度和相变,以促进工艺放大、过程分析以及未来冷冻容器的定制。使用牛血清白蛋白从冰芯样品中确定蛋白质的冰晶浓缩。研究了冷冻兔肌肉 L-乳酸脱氢酶(LDH)溶液中的活性、聚集和结构扰动。CFD 模拟与温度和相变的高分辨率实验测量具有良好的定性和定量一致性,还允许估计空间冰晶浓缩模式。LDH 在实验室规模系统中表现出对冷冻的稳定性,表明在某些条件下冰晶浓缩具有保护作用。该实验室规模冷冻容器与精确 CFD 建模的结合将允许在高级规模下对 F/T 过程进行更深入的研究,因此代表了朝着更好的工艺理解迈出的重要一步。