Raman spectroscopic based chemometric models to support a dynamic capacitance based cell culture feeding strategy

被引:17
|
作者
Rafferty, Carl [1 ,2 ]
O'Mahony, Jim [2 ]
Rea, Rosemary [2 ]
Burgoyne, Barbara [3 ]
Balss, Karin M. [4 ]
Lyngberg, Olav [4 ]
O'Mahony-Hartnett, Caitlin [1 ]
Hill, Dan [5 ]
Schaefer, Eugene [6 ]
机构
[1] Janssen Sci Ireland UC, BioTherapeut Dev, Cork, Ireland
[2] Cork Inst Technol, Biol Sci, Cork, Ireland
[3] Janssen Sci Ireland UC, Prod Qual Management, Cork, Ireland
[4] Adv Technol Ctr Excellence, Janssen Supply Grp, Raritan, NJ USA
[5] Biogen, Global Proc Analyt, Res Triangle Pk, NC USA
[6] Janssen Res & Dev Malvern, DPDS, BioTherapeut Dev, Malvern, PA USA
关键词
Cell culture; Raman spectroscopy; Capacitance; Dynamic feeding; Chemometric modelling; DIELECTRIC-SPECTROSCOPY; BATCH; DENSITY; GLUCOSE; PARAMETERS; REGRESSION; BIOMASS;
D O I
10.1007/s00449-020-02336-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Multiple process analytical technology (PAT) tools are now being applied in tandem for cell culture. Research presented used two in-line probes, capacitance for a dynamic feeding strategy and Raman spectroscopy for real-time monitoring. Data collected from eight batches at the 15,000 L scale were used to develop process models. Raman spectroscopic data were modelled using Partial Least Squares (PLS) by two methods-(1) use of the full dataset and (2) split the dataset based on the capacitance feeding strategy. Root mean square error of prediction (RMSEP) for the first model method of capacitance was 1.54 pf/cm and the second modelling method was 1.40 pf/cm. The second Raman method demonstrated results within expected process limits for capacitance and a 0.01% difference in total nutrient feed compared to the capacitance probe. Additional variables modelled using Raman spectroscopy were viable cell density (VCD), viability, average cell diameter, and viable cell volume (VCV).
引用
收藏
页码:1415 / 1429
页数:15
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