| Literature DB >> 2800464 |
A Farrugia1, D Spiers, I Young, A Oates, R Herrington, F Damianos.
Abstract
Using pilot-scale production of our present factor IX (II and X) concentrate, we have studied the effects of starting plasma source and processing parameter on two in-vitro indicators of product quality - yield and thrombogenic potential. Plasma source did not affect factor IX yield but had a marked effect on thrombogenic potential. Factor IX concentrates produced from plasma derived through centrifugation-based technology showed significantly higher thrombogenic potential than products derived from plasma derived through a filtration-based system. Removal of Cohn fraction I prior to ion-exchange chromatography resulted in a drop in factor IX yield and thrombogenic potential, as did heat treatment to 80 degrees C for 72 h. We conclude that a membrane-filtration-based plasmapheresis system may be the preferred method of plasma procurement for factor IX concentrate production.Mesh:
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Year: 1989 PMID: 2800464 DOI: 10.1111/j.1423-0410.1989.tb04975.x
Source DB: PubMed Journal: Vox Sang ISSN: 0042-9007 Impact factor: 2.144