METHODS AND STRATEGIES AVAILABLE FOR THE PROCESS-CONTROL AND OPTIMIZATION OF MONOCLONAL-ANTIBODY PRODUCTION

被引:7
作者
FU, PC [1 ]
BARFORD, JP [1 ]
机构
[1] UNIV SYDNEY,DEPT CHEM ENGN,SYDNEY,NSW 2006,AUSTRALIA
关键词
ANIMAL CELLS; CELLULAR METABOLISM; CULTIVATION; HYBRIDOMAS; MODELING; MONOCLONAL ANTIBODY; PROCESS CONTROL; OPTIMIZATION; SIMULATION;
D O I
10.1007/BF00749618
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 objective of this paper is to explore the range of methods and strategies available for the process control and optimization of monoclonal antibody production by hybridoma cell culture. Emphasis will be placed on the choice of the level of complexity incorporated into the process control and optimisation procedure. It will be shown that the behaviour of hybridomas in culture is influenced by sophisticated cellular metabolic activities and various interactive environmental factors and that the understanding and modelling of the way hybridomas grow in the bioreactor should enable optimisation of bioreactor operating conditions to achieve maximum monoclonal antibody formation. However, due to the lack of on-line instrumentation of important biological variables and the incomplete knowledge of hybridoma cultivation process, there exist many limitations and challenges to the advent of applications of process control and optimisation in this field. To solve the problem, introduction of industrially practical biological measurements and development of new control concepts are inevitable. At the end of this paper, we shall discuss possible schemes for the control of the physiological state of cells in order that balanced cell growth and maximum monoclonal antibody synthesis may be achieved.
引用
收藏
页码:219 / 232
页数:14
相关论文
共 75 条
[1]   SPECIFIC MONOCLONAL-ANTIBODY PRODUCTIVITY AND THE CELL CYCLE-COMPARISONS OF BATCH, CONTINUOUS AND PERFUSION CULTURES [J].
ALRUBEAI, M ;
EMERY, AN ;
CHALDER, S ;
JAN, DC .
CYTOTECHNOLOGY, 1992, 9 (1-3) :85-97
[2]   LARGE-SCALE PRODUCTION OF MONOCLONAL-ANTIBODIES IN SUSPENSION-CULTURE [J].
BACKER, MP ;
METZGER, LS ;
SLABER, PL ;
NEVITT, KL ;
BODER, GB .
BIOTECHNOLOGY AND BIOENGINEERING, 1988, 32 (08) :993-1000
[3]   LIMITATION OF GROWTH-RATE BY 2 COMPLEMENTARY NUTRIENTS - SOME ELEMENTARY BUT NEGLECTED CONSIDERATIONS [J].
BALTZIS, BC ;
FREDRICKSON, AG .
BIOTECHNOLOGY AND BIOENGINEERING, 1988, 31 (01) :75-86
[4]  
BARFORD J, 1991, PRODUCTION OF BIOLOGICALS FROM ANIMAL CELLS IN CULTURE, P631
[5]   SIMULATION OF ANIMAL-CELL METABOLISM [J].
BARFORD, JP ;
PHILLIPS, PJ ;
HARBOUR, C .
CYTOTECHNOLOGY, 1992, 10 (01) :63-74
[6]   A STRUCTURED KINETIC MODELING FRAMEWORK FOR THE DYNAMICS OF HYBRIDOMA GROWTH AND MONOCLONAL-ANTIBODY PRODUCTION IN CONTINUOUS SUSPENSION-CULTURES [J].
BATT, BC ;
KOMPALA, DS .
BIOTECHNOLOGY AND BIOENGINEERING, 1989, 34 (04) :515-531
[7]  
BELLGARDT KH, 1985, MODELLING CONTROL BU, P55
[8]   A STRUCTURED MODEL FOR MONOCLONAL-ANTIBODY SYNTHESIS IN EXPONENTIALLY GROWING AND STATIONARY PHASE HYBRIDOMA CELLS [J].
BIBILA, T ;
FLICKINGER, MC .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 37 (03) :210-226
[9]  
BIBILA T, 1993, UNPUB BIOTECHNOL BIO
[10]   USE OF A STRUCTURED KINETIC-MODEL OF ANTIBODY-SYNTHESIS AND SECRETION FOR OPTIMIZATION OF ANTIBODY-PRODUCTION SYSTEMS .1. STEADY-STATE ANALYSIS [J].
BIBILA, TA ;
FLICKINGER, MC .
BIOTECHNOLOGY AND BIOENGINEERING, 1992, 39 (03) :251-261