Defining process design space for biotech products:: Case study of Pichia pastoris fermentation

被引:70
作者
Harms, Jean [1 ]
Wang, Xiangyang [1 ]
Kim, Tina [1 ]
Yang, Xiaoming [1 ]
Rathore, Anurag S. [1 ]
机构
[1] Amgen Inc, Proc Dev, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1021/bp070338y
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
The concept of "design space" has been proposed in the ICH Q8 guideline and is gaining momentum in its application in the biotech industry. It has been defined as "the multidimensional combination and interaction of input variables (e.g., material attributes) and process parameters that have been demonstrated to provide assurance of quality." This paper presents a stepwise approach for defining process design space for a biologic product. A case study, involving P. pastoris fermentation, is presented to facilitate this. First, risk analysis via Failure Modes and Effects Analysis (FMEA) is performed to identify parameters for process characterization. Second, small-scale models are created and qualified prior to their use in these experimental studies. Third, studies are designed using Design of Experiments (DOE) in order for the data to be amenable for use in defining the process design space. Fourth, the studies are executed and the results analyzed for decisions on the criticality of the parameters as well as on establishing process design space. For the application under consideration, it is shown that the fermentation unit operation is very robust with a wide design space and no critical operating parameters. The approach presented here is not specific to the illustrated case study. It can be extended to other biotech unit operations and processes that can be scaled down and characterized at small scale.
引用
收藏
页码:655 / 662
页数:8
相关论文
共 20 条
[11]  
RATHORE AS, 2005, BIOPHARM INT MAR, P60
[12]   Optimization and scale up of industrial fermentation processes [J].
Schmidt, FR .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2005, 68 (04) :425-435
[13]  
SEELY JE, 2003, BIOPHARM INT AUG, P24
[14]  
Seely R, 2005, PROCESS VALIDATION M, P31
[15]   Process characterization for metal-affinity chromatography of an Fc fusion protein: a design-of-experiments approach [J].
Shukla, AA ;
Sorge, L ;
Boldman, J ;
Waugh, S .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2001, 34 (02) :71-80
[16]   Causes of proteolytic degradation of secreted recombinant proteins produced in methylotrophic yeast Pichia pastoris:: Case study with recombinant ovine interferon-τ [J].
Sinha, J ;
Plantz, BA ;
Inan, M ;
Meagher, MM .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 89 (01) :102-112
[17]   Improved production of recombinant ovine interferon-τ by Mut+ strain of Pichia pastoris using an optimized methanol feed profile [J].
Sinha, J ;
Plantz, BA ;
Zhang, WH ;
Gouthro, M ;
Schlegel, V ;
Liu, CP ;
Meagher, MM .
BIOTECHNOLOGY PROGRESS, 2003, 19 (03) :794-802
[18]   Effect of methanol feeding strategies on production and yield of recombinant mouse endostatin from Pichia pastoris [J].
Trinh, LB ;
Phue, JN ;
Shiloach, J .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 82 (04) :438-444
[19]  
Zhang WH, 2000, BIOTECHNOL BIOENG, V70, P1, DOI 10.1002/1097-0290(20001005)70:1<1::AID-BIT1>3.0.CO
[20]  
2-Y