Heat flux sensor to create a design space for freeze-drying development

被引:13
作者
Carfagna, Marco [1 ,2 ]
Rosa, Monica [1 ]
Lucke, Matthias [1 ]
Hawe, Andrea [1 ]
Friess, Wolfgang [2 ]
机构
[1] Coriolis Pharma Res GmbH, Fraunhoferstr 18B, D-82152 Planegg, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Pharm Pharmaceut Technol & Biopharmaceut, D-81377 Munich, Germany
关键词
Freeze-drying; QbD; PAT; Heat flux sensor; Gravimetric technique; Design space; MANOMETRIC TEMPERATURE-MEASUREMENT; LASER ABSORPTION-SPECTROSCOPY; PRODUCT TEMPERATURE; RAPID-DETERMINATION; TRANSFER PARAMETERS; SCALE-UP; LYOPHILIZATION; QUALITY; MASS; TECHNOLOGY;
D O I
10.1016/j.ejpb.2020.05.028
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Freeze-drying methodology requires an in-depth understanding and characterization for optimal processing of biopharmaceuticals. Particularly the primary drying phase, the longest and most expensive stage of the process, is of interest for optimization. The currently used process analytical technology (PAT) tools give highly valuable insights but come with limitations. Our study describes, for the first time, the application of a heat flux sensor (HFS) to build a primary drying design space and predict the process evolution. First, the heat transfer coefficient (K-v) generated by HFS and by the most accurate, but time-consuming and invasive, gravimetric method were compared. Second, the applicability to generate a design space was tested and verified. Obtained results revealed a good agreement of the values generated from this new and fast HFS compared to the gravimetric determination. Additionally, residual moisture assessed by Karl-Fischer titration and frequency modulated spectroscopy (FMS) support the quality of the obtained predictions. Thus, the HFS approach can substantially accelerate evaluation, development and transfer of a freeze-drying cycle.
引用
收藏
页码:84 / 94
页数:11
相关论文
共 50 条
[31]  
PIKAL M J, 1985, Journal of Parenteral Science and Technology, V39, P115
[32]   The nonsteady state modeling of freeze drying: In-process product temperature and moisture content mapping and pharmaceutical product quality applications [J].
Pikal, MJ ;
Cardon, S ;
Bhugra, C ;
Jameel, F ;
Rambhatla, S ;
Mascarenhas, WJ ;
Akay, HU .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2005, 10 (01) :17-32
[33]   MASS AND HEAT-TRANSFER IN VIAL FREEZE-DRYING OF PHARMACEUTICALS - ROLE OF THE VIAL [J].
PIKAL, MJ ;
ROY, ML ;
SHAH, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (09) :1224-1237
[34]  
Pisano R, 2011, DEVELOPMENTS IN HEAT TRANSFER, P91
[35]  
Rambhatla Shailaja, 2003, AAPS PharmSciTech, V4, pE14
[36]  
Rey L., 2004, FREEZE DRYING LYOPHI
[37]  
Schneid S., 2007, P AAPS ANN M SAN DIE
[38]   3D mathematical modelling to understand atypical heat transfer observed in vial freeze-drying [J].
Scutella, B. ;
Plana-Fattori, A. ;
Passot, S. ;
Bourles, E. ;
Fonseca, F. ;
Flick, D. ;
Trelea, I. C. .
APPLIED THERMAL ENGINEERING, 2017, 126 :226-236
[39]   Determination of the dried product resistance variability and its influence on the product temperature in pharmaceutical freeze-drying [J].
Scutella, Bernadette ;
Trelea, Ioan Cristian ;
Bourles, Erwan ;
Fonseca, Fernanda ;
Passot, Stephanie .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2018, 128 :379-388
[40]   How Vial Geometry Variability Influences Heat Transfer and Product Temperature During Freeze-Drying [J].
Scutella, Bernadette ;
Passot, Stehanie ;
Bourles, Erwan ;
Fonseca, Fernanda ;
Trelea, Ioan Cristian .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 106 (03) :770-778