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A mechanistic study on the destabilization of whole inactivated influenza virus vaccine in gastric environment

tetano

Editor, Senior Moderator
PLoS One. 2013 Jun 11;8(6):e66316. doi: 10.1371/journal.pone.0066316. Print 2013.
A mechanistic study on the destabilization of whole inactivated influenza virus vaccine in gastric environment.
Choi HJ, Ebersbacher CF, Kim MC, Kang SM, Montemagno CD.
Source

School of Energy, Environmental, Biological and Medical Engineering University of Cincinnati, Cincinnati, Ohio, United States of America.
Abstract

Oral immunization using whole inactivated influenza virus vaccine promises an efficient vaccination strategy. While oral vaccination was hampered by harsh gastric environment, a systematic understanding about vaccine destabilization mechanisms was not performed. Here, we investigated the separate and combined effects of temperature, retention time, pH, and osmotic stress on the stability of influenza vaccine by monitoring the time-dependent morphological change using stopped-flow light scattering. When exposed to osmotic stress, clustering of vaccine particles was enhanced in an acidic medium (pH 2.0) at ≥25?C. Fluorescence spectroscopic studies showed that hyper-osmotic stress at pH 2.0 and 37?C caused a considerable increase in conformational change of antigenic proteins compared to that in acidic iso-osmotic medium. A structural integrity of membrane was destroyed upon exposure to hyper-osmotic stress, leading to irreversible morphological change, as observed by undulation in stopped-flow light scattering intensity and transmission electron microscopy. Consistent with these analyses, hemagglutination activity decreased more significantly with an increasing magnitude of hyper-osmotic stress than in the presence of the hypo- and iso-osmotic stresses. This study shows that the magnitude and direction of the osmotic gradient has a substantial impact on the stability of orally administrated influenza vaccine.

PMID:
23776657
[PubMed - in process]
PMCID:
PMC3679046

Free full text

http://www.ncbi.nlm.nih.gov/pubmed/23776657
 
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