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A novel primary amine-based anion exchange membrane adsorber
- Source :
- Journal of Chromatography A. 1218:5386-5392
- Publication Year :
- 2011
- Publisher :
- Elsevier BV, 2011.
-
Abstract
- A novel anion exchange membrane adsorber is presented which shows excellent impurity removal under different buffer conductivities ranging from 2 to 27 mS/cm. The membrane utilizes a primary amine ligand (polyallylamine) and was designed specifically to bind impurities at high salt concentrations. Studies with DNA, endotoxin, and virus spiked into buffer at varying salt conditions were done, resulting in clearance of >3, 4, and 4 LRV, respectively, with negligible change on increasing salt up to 27 mS/cm conductivities. Verification of virus removal in mAb feedstocks is also shown. The data are compared with other membrane adsorbers and a conventional resin which utilize traditional chemistries to demonstrate improved purification performance with the primary amine ligand. Additional data on scale-up of the membrane adsorber device is discussed. A stacked flat-sheet design was implemented to ensure linear scale-up of performance using bovine serum albumin (BSA) as a model. The linearly scalable device, coupled with the highly effective membrane for virus, DNA, and endotoxin removal, represents a step forward in polishing technology for the purification of monoclonal antibodies and recombinant proteins.
- Subjects :
- Salt (chemistry)
Biochemistry
Buffer (optical fiber)
Analytical Chemistry
law.invention
law
Impurity
Animals
Humans
Amines
Bovine serum albumin
chemistry.chemical_classification
Chromatography
biology
Ion exchange
Chemistry
Organic Chemistry
Proteins
Membranes, Artificial
Serum Albumin, Bovine
DNA
General Medicine
Chromatography, Ion Exchange
Recombinant Proteins
Endotoxins
Membrane
Viruses
Recombinant DNA
biology.protein
Cattle
Amine gas treating
Adsorption
Subjects
Details
- ISSN :
- 00219673
- Volume :
- 1218
- Database :
- OpenAIRE
- Journal :
- Journal of Chromatography A
- Accession number :
- edsair.doi.dedup.....3cec5d9ebb8afda6d925b51c79115caf