Effects of ultra-/diafiltration conditions on present aggregates in human immunoglobulin G preparations

被引:19
作者
Ahrer, K
Buchacher, A
Iberer, G
Jungbauer, A
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Biotechnol, A-1190 Vienna, Austria
[2] Octapharma Pharmazeut Prod GembH, A-1100 Vienna, Austria
关键词
cross-flow filtration; light scattering; immunoglobulin; aggregation; ionic strength;
D O I
10.1016/j.memsci.2005.08.018
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Small traces of aggregates may cause reduced stability of human immunoglobulin G preparations. Ultra-/diafiltration as last step before formulation could also contribute to aggregate formation or depletion. One of the key challenges is to find a sensitive analytical method for the early detection of initial aggregation. Dynamic light scattering was applied to detect differences in the aggregate pattern during cross-flow filtration of human immunoglobulin preparations. The change of ionic strength of the process solution during diatiltration significantly influenced the aggregate pattern. Other causes for aggregation, such as flow induced shear stress or high local protein concentrations due to the build-up of a gel layer, did not significantly influence the formation of aggregates. The use of weak buffered solutions suppressed aggregate formation and as a positive effect permeate flux was increased during diatiltration. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 115
页数:8
相关论文
共 35 条
[11]  
*FOOD DRUG ADM, 2004, GUID IND DRUG SUBST
[12]  
GERHART EM, 1993, STEADY INCOMPRESSIBL, P462
[13]   Streptokinase recovery by cross-flow microfiltration: Study of enzyme denaturation [J].
HernandezPinzon, I ;
Millan, F ;
Bautista, J .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1997, 61 (08) :1240-1243
[14]   Effect of aggregated protein sizes on the flux of protein solution through microporous membranes [J].
Higuchi, A ;
Kyokon, M ;
Murayama, S ;
Yokogi, M ;
Hirasaki, T ;
Manabe, SI .
JOURNAL OF MEMBRANE SCIENCE, 2004, 236 (01) :137-144
[15]   Enhanced microfiltration of γ-globulin solution upon treatment of NaCl addition and/or DNase digestion [J].
Higuchi, A ;
Nemoto, M ;
Koyama, H ;
Hirano, K ;
Yoon, BO ;
Hara, M ;
Yokogi, M ;
Manabe, SI .
JOURNAL OF MEMBRANE SCIENCE, 2002, 210 (02) :369-378
[16]   Permeation of γ-globulin through microporous membranes in the presence of trace DNA [J].
Higuchi, A ;
Komuro, A ;
Hirano, K ;
Yoon, BO ;
Hara, M ;
Hirasaki, T ;
Nishimoto, Y ;
Yokogi, M ;
Manabe, SI .
JOURNAL OF MEMBRANE SCIENCE, 2001, 186 (01) :9-18
[17]   The effect of protein-protein and protein-membrane interactions on membrane fouling in ultrafiltration [J].
Huisman, IH ;
Prádanos, P ;
Hernández, A .
JOURNAL OF MEMBRANE SCIENCE, 2000, 179 (1-2) :79-90
[18]  
Johnstone AP, 1996, IMMUNOCHEMISTRY PRAC
[20]   PROCESS-DEVELOPMENT FOR THE RECOVERY AND PURIFICATION OF RECOMBINANT PROTEIN-G [J].
LEE, SM ;
ESSIG, NZ ;
LEE, TK .
JOURNAL OF BIOTECHNOLOGY, 1992, 26 (2-3) :213-229