Related Experiment Video
Updated: Aug 10, 2026

Isolation and Characterization Of Chimeric Human Fc-expressing Proteins Using Protein A Membrane Adsorbers And A Streamlined Workflow
Published on: January 8, 2014
Large-scale purification of antisense oligonucleotides by high-performance membrane adsorber chromatography
R R Deshmukh1, T N Warner, F Hutchison
1Isis Pharmaceuticals, Inc., Carlsbad, CA 92008, USA. Deshmur@war.wyeth.com
Abstract:
Very high flux ion-exchange membranes were utilized for a novel purification of antisense oligonucleotides (20-mer). Strong anion-exchange membranes were produced by attaching polymeric ligands onto a microporous cellulosic matrix. The oligonucleotides purified were therapeutic single-stranded phosphorothioates deoxyribonucleotides. Although small-scale membrane devices (15 cm2) had similar resolution to traditional chromatographic columns; their throughputs were superior. Greater than a 1300-fold scale-up produced very similar purity and yields of the phosphorothionate product. Scale-up experiments were conducted with a 2 m2 surface area membrane module. These modules were easily capable of very high throughputs of 0.5 to 2 l/min. High purity and yields were achieved by both step and linear gradient elution.
Related Concept Videos
Detergent Purification of Membrane Proteins
Affinity Chromatography

