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dc.contributor.authorHassett, Kimberly J.
dc.contributor.authorVance, David J.
dc.contributor.authorJain, Nishant K.
dc.contributor.authorShani, Neha
dc.contributor.authorRabia, Lilia A.
dc.contributor.authorCousins, Megan C.
dc.contributor.authorJoshi, Sangeeta B.
dc.contributor.authorVolkin, David B.
dc.contributor.authorMiddaugh, C. Russell
dc.contributor.authorMantis, Nicholas J.
dc.contributor.authorCarpenter, John F.
dc.contributor.authorRandolph, Theodore W.
dc.date.accessioned2017-04-25T18:22:10Z
dc.date.available2017-04-25T18:22:10Z
dc.date.issued2015-02
dc.identifier.citationHassett, K. J., Vance, D. J., Jain, N. K., Sahni, N., Rabia, L. A., Cousins, M. C., … Randolph, T. W. (2015). Glassy-State Stabilization of a Dominant Negative Inhibitor Anthrax Vaccine Containing Aluminum Hydroxide and Glycopyranoside Lipid A Adjuvants. Journal of Pharmaceutical Sciences, 104(2), 627–639. http://doi.org/10.1002/jps.24295en_US
dc.identifier.urihttp://hdl.handle.net/1808/23768
dc.description.abstractDuring transport and storage, vaccines may be exposed to temperatures outside of the range recommended for storage, potentially causing efficacy losses. To better understand and prevent such losses, Dominant Negative Inhibitor (DNI), a recombinant protein antigen for a candidate vaccine against anthrax, was formulated as a liquid and as a glassy lyophilized powder with the adjuvants aluminum hydroxide and glycopyranoside lipid A (GLA). Freeze-thawing of the liquid vaccine caused the adjuvants to aggregate and decreased its immunogenicity in mice. Immunogenicity of liquid vaccines also decreased when stored at 40 °C for 8 weeks, as measured by decreases in neutralizing antibody titers in vaccinated mice. Concomitant with efficacy losses at elevated temperatures, changes in DNI structure were detected by fluorescence spectroscopy and increased deamidation was observed by capillary isoelectric focusing (cIEF) after only 1 week of storage of the liquid formulation at 40 °C. In contrast, upon lyophilization, no additional deamidation after 4 weeks at 40 °C and no detectable changes in DNI structure or reduction in immunogenicity after 16 weeks at 40 °C was observed. Vaccines containing aluminum hydroxide and GLA elicited higher immune responses than vaccines adjuvanted with only aluminum hydroxide, with more mice responding to a single dose.en_US
dc.publisherElsevieren_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectLyophilizationen_US
dc.subjectAnthraxen_US
dc.subjectDominant Negative Inhibitoren_US
dc.subjectVaccine Adjuvantsen_US
dc.subjectAluminumen_US
dc.subjectGlycopyranoside Lipid A (GLA)en_US
dc.subjectVaccinesen_US
dc.subjectFreeze-thawen_US
dc.subjectStabilityen_US
dc.subjectFormulationen_US
dc.titleGlassy-State Stabilization of a Dominant Negative Inhibitor Anthrax Vaccine Containing Aluminum Hydroxide and Glycopyranoside Lipid A Adjuvantsen_US
dc.typeArticleen_US
kusw.kuauthorJain, Nishant K.
kusw.kuauthorSahni, Neha
kusw.kuauthorJoshi, Sangeeta B.
kusw.kuauthorVolkin, David B.
kusw.kuauthorMiddaugh, C. Russell
kusw.kudepartmentPharmaceutical Chemistryen_US
dc.identifier.doi10.1002/jps.24295en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC4312196en_US
dc.rights.accessrightsopenAccess


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This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.