Interaction of mammalian cell culture broth with adsorbents in expanded bed adsorption of monoclonal antibodies

被引:39
作者
Feuser, J
Halfar, M
Lütkemeyer, D
Ameskamp, N
Kula, MR
Thömmes, J
机构
[1] Univ Dusseldorf, Inst Enzymtechnol, D-52426 Julich, Germany
[2] Univ Bielefeld, Tech Fak, D-33501 Bielefeld, Germany
关键词
expanded bed adsorption; monoclonal antibody; protein purification; ion exchange chromatography; affinity chromatography; hybridoma cells;
D O I
10.1016/S0032-9592(98)00083-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interaction of a mammalian cell culture broth with two commercially available adsorbents for the use in expanded bed adsorption (EBA) has been studied. A cation exchange resin (Streamline SP) and an affinity adsorbent (Streamline rProtein A) were compared with regard to adsorption of hybridoma cells during sample application as well as potential cell damage. The results showed that hybridoma cells interact significantly with an expanded bed of cation exchange adsorbents but not with the Protein A adsorbent. After application of 17-20 sedimented bed volumes a saturation of the Streamline SP resin with cells was noted. With both adsorbents no measurable cell damage was found acid IgG, was recovered in approximately 95% yield. The capacity for IgG, adsorption at 3% breakthrough was 2.7 mg IgG(1)/ml Streamline rProtein A at a constant fluid velocity of 380 cm/h and 1.0 mg IgG(1)/ml Streamline SP at 215-240 cm/h fluid velocity. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:159 / 165
页数:7
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