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Phenomenex, Inc.. (6/1/11). "Press Release: Phenomenex Announces New Method for EPO (Erythropoietin) Impurity Analysis. New Solution Meets Growing Method Development Needs as Patents Expire". Torrance, CA.

	Organisation	Phenomenex Inc.
	Group	Phenomenex (Group)
	Product	BioSep-SEC-s2000 column (product series)
	Person	McGinley, Michael (Phenomenex 201105 HPLC Product Manager)

Phenomenex Inc., a global leader in the research and manufacture of advanced technologies for the separation sciences, announces the publication of a new method for the analysis of aggregates of EPO, a widely manufactured recombinant biosimilar protein therapeutic. As patent protection expires for the original EPO drugs, many companies are working to produce generic versions, resulting in a skyrocketing need for method development and validation. The new gel filtration chromatography (GFC) method developed by Phenomenex quantifies aggregates in these recombinant therapeutics using a BioSep-SEC-s2000 series column, which provides a superior separation window for low-molecular-weight proteins.

"Our published data shows a clear advantage in using this BioSep column and our GFC method, over the columns used in the past," explains Michael McGinley, HPLC product manager for Phenomenex. "This rugged yet simple method effectively analyzes the amount of aggregate and dimer in these low-molecular-weight samples."

A technical note on the new Phenomenex EPO method has just been published and can be accessed at: www.phenomenex.com/epo.

For more information regarding this article please contact:
Phenomenex Press Room
Phone: (310) 212-0555

Record changed: 2011-11-25

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