Comparison of Different Methods of Purification and Concentration in Production of Influenza Vaccine


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Resumo

The overwhelming majority of influenza vaccines are prepared with the use of chicken embryo allantoic fluid. The presence of ovalbumin (this protein constitutes >60% total protein in the allantoic fluid) in the vaccine can lead to severe allergy. Hence, effective reduction of ovalbumin content is of crucial importance for vaccine production. We compared two methods of purification and concentration of influenza virus: zonal gradient ultracentrifugation and combined ultrafiltration/diafiltration and exclusion chromatography protocol, used for fabrication of seasonal vaccines. Combined chromatography is comparable with zonal centrifugation protocol by the results of ovalbumin removal (to meet standard requirements).

Sobre autores

N. Asanzhanova

Research Institute of Biological Safety Problems

Autor responsável pela correspondência
Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region

Sh. Ryskeldinova

Research Institute of Biological Safety Problems

Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region

O. Chervyakova

Research Institute of Biological Safety Problems

Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region

B. Khairullin

Research Institute of Biological Safety Problems

Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region

M. Kasenov

Research Institute of Biological Safety Problems

Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region

K. Tabynov

Research Institute of Biological Safety Problems

Email: anurika@mail.ru
Cazaquistão, Gvardeiskii settlement, Zhambyl Region


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2017

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