The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 02, 2014

Filed:

Apr. 20, 2012
Applicants:

Paola Rossi, Castiglione di Gafagnana, IT;

Ilaria Nardini, Barga, IT;

Pierangelo Giovacchini, Lammari-Capannori, IT;

Filippo Mori, Lucca, IT;

Claudio Farina, Pisa, IT;

Inventors:

Paola Rossi, Castiglione di Gafagnana, IT;

Ilaria Nardini, Barga, IT;

Pierangelo Giovacchini, Lammari-Capannori, IT;

Filippo Mori, Lucca, IT;

Claudio Farina, Pisa, IT;

Assignee:

Kedrion S.p.A., Castel Vecchio Pascoli, IT;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K 38/00 (2006.01); C07K 14/745 (2006.01); C07K 14/75 (2006.01); C07K 1/22 (2006.01); C07K 1/36 (2006.01); C07K 1/18 (2006.01); G01N 30/02 (2006.01); C07K 1/16 (2006.01);
U.S. Cl.
CPC ...
C07K 1/16 (2013.01); C07K 14/745 (2013.01);
Abstract

The present invention provides a process for purifying FV starting from human plasma or a fractionation intermediate thereof, that is simple, scalable to the industrial level and relatively inexpensive compared to the methods described in the literature to date. The invention consists of the use of two anion exchange chromatography steps, the first of which has the purpose of separating the FV from the PTC component factors, while the second has the purpose of isolating the protein of interest from the majority of plasma proteins by means of selective interaction with the weak anion exchange support used. The process developed has also had a viral inactivation step and a viral removal step included, contributing to the safety of the final product obtained, without however significantly altering the process total recovery of FV, and without necessitating the introduction of additional steps for eliminating the inactivating agents used, thanks to the order in which the various steps are conducted. The process described in the present invention also enables an FV concentrate to be obtained that is stable once frozen at −20° C.


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