Literature DB >> 21651939

Foot and mouth disease (FMD) virus: quantification of whole virus particles during the vaccine manufacturing process by size exclusion chromatography.

Marcelo A Spitteler1, Ignacio Fernández, Erika Schabes, Alejandro Krimer, Emmanuel G Régulier, Mariela Guinzburg, Eliana Smitsaart, M Susana Levy.   

Abstract

Foot and mouth disease (FMD) is a highly infectious viral disease that affects cattle, sheep, goats and swine causing severe economic losses worldwide. The efficacy of inactivated vaccines is critically dependent on the integrity of foot and mouth disease virus (FMDV) particles. The recommended method to quantify the active ingredient of vaccines is the 140S quantitative sucrose density gradient analysis. This method has been an immensely valuable tool over the past three decades but it is highly operator dependent and difficult to automate. We developed a method to quantify FMDV particles during the vaccine manufacturing process that is based on separation of components by size-exclusion chromatography and measurement of virus by absorption at 254nm. The method is linear in the 5-70μg/mL range, it is applicable to different FMDV strains, and has a good correlation with the 140S test. The proposed method uses standard chromatographic media and it is amenable to automation. The method has potential as a process analytical technology and for control of final product by manufacturers, international vaccine banks and regulatory agencies.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21651939     DOI: 10.1016/j.vaccine.2011.05.078

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  6 in total

1.  Genetic identification and serological evaluation of commercial inactivated foot-and-mouth disease virus vaccine in pigs.

Authors:  Sang H Je; Taeyong Kwon; Sung J Yoo; Dong-Uk Lee; Sang Won Seo; Jeong J Byun; Jeong Y Shin; Young S Lyoo
Journal:  Clin Exp Vaccine Res       Date:  2018-07-31

2.  Investigation of cell culture conditions for optimal foot-and-mouth disease virus production.

Authors:  Veronika Dill; Aline Zimmer; Martin Beer; Michael Eschbaumer
Journal:  BMC Biotechnol       Date:  2019-06-07       Impact factor: 2.563

Review 3.  Cell culture propagation of foot-and-mouth disease virus: adaptive amino acid substitutions in structural proteins and their functional implications.

Authors:  Veronika Dill; Michael Eschbaumer
Journal:  Virus Genes       Date:  2019-11-27       Impact factor: 2.332

4.  Application of Heparin Affinity Chromatography to Produce a Differential Vaccine without Eliciting Antibodies against the Nonstructural Proteins of the Serotype O Foot-and-Mouth Disease Viruses.

Authors:  Sun Young Park; Jung-Min Lee; Ah-Young Kim; Sang Hyun Park; Jae-Seok Kim; Hyejin Kim; Jung-Won Park; Jong-Hyeon Park; Young-Joon Ko; Choi-Kyu Park
Journal:  Viruses       Date:  2020-12-07       Impact factor: 5.048

5.  Quantitative Detection of the Foot-And-Mouth Disease Virus Serotype O 146S Antigen for Vaccine Production Using a Double-Antibody Sandwich ELISA and Nonlinear Standard Curves.

Authors:  Xia Feng; Jun-Wu Ma; Shi-Qi Sun; Hui-Chen Guo; Ya-Min Yang; Ye Jin; Guang-Qing Zhou; Ji-Jun He; Jian-Hong Guo; Shu-yun Qi; Mi Lin; Hu Cai; Xiang-Tao Liu
Journal:  PLoS One       Date:  2016-03-01       Impact factor: 3.240

6.  Isolation of Single-Domain Antibody Fragments That Preferentially Detect Intact (146S) Particles of Foot-and-Mouth Disease Virus for Use in Vaccine Quality Control.

Authors:  Michiel M Harmsen; Julian Seago; Eva Perez; Bryan Charleston; Phaedra L Eblé; Aldo Dekker
Journal:  Front Immunol       Date:  2017-08-17       Impact factor: 7.561

  6 in total

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