Formulation and coating of microneedles with inactivated influenza virus to improve vaccine stability and immunogenicity

• Type of Material: Article
• Authors: Yeu-Chun Kim, Georgia Institute of Technology; Fu-Shi Quan, Emory University; Richard W Compans, Emory University; Sang-Moo Kang, Emory University; Mark R. Prausnitz, Emory University
• Language: English
• Date: 2010-03-03
• Publisher: Elsevier: 12 months
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2009 Elsevier B.V. All rights reserved.
• License: Creative Commons Attribution-NonCommerical-NoDerivs 3.0 Unported
• Final Published Version (URL): http://dx.doi.org/10.1016/j.jconrel.2009.10.013
• Title of Journal or Parent Work: Journal of Controlled Release
• ISSN: 0168-3659
• Volume: 142
• Issue: 2
• Start Page: 187
• End Page: 195
• Grant/Funding Information: It was supported in part by NIH grants R01-EB006369 (M.R.P.), AI0680003 (R.W.C.), AI074579-01 (R.W.C), SERCEB (R.W.C) and the Korea Ginseng Society (S.M.K).
• Keywords: microneedle; influenza virus; inactivated virus vaccine; trehalose
• Research Categories: Health Sciences, Immunology; Engineering, Biomedical

Abstract

Microneedle patches coated with solid-state influenza vaccine have been developed to improve vaccine efficacy and patient coverage. However, dip coating microneedles with influenza vaccine can reduce antigen activity. In this study, we sought to determine the experimental factors and mechanistic pathways by which inactivated influenza vaccine can lose activity, as well as develop and assess improved microneedle coating formulations that protect the antigen from activity loss. After coating microneedles using a standard vaccine formulation, antigenicity was reduced to just 2%, as measured by hemagglutination activity. The presence of carboxymethylcellulose, which was added to increase viscosity of the coating formulation, was shown to contribute to vaccine activity loss. After screening a panel of candidate stabilizers, the addition of trehalose to the coating formulation was shown to protect the antigen and retain 48–82% antigen activity for all three major strains of seasonal influenza: H1N1, H3N2 and B. Influenza vaccine coated in this way also exhibited thermal stability, such that activity loss was independent of temperature over the range of 4 – 37°C for 24 h. Dynamic light scattering measurements showed that antigen activity loss was associated with virus particle aggregation, and that stabilization using trehalose largely blocked this aggregation. Finally, microneedles using an optimized vaccine coating formulation were applied to the skin to vaccinate mice. Microneedle vaccination induced robust systemic and functional antibodies and provided complete protection against lethal challenge infection similar to conventional intramuscular injection. Overall, these results show that antigen activity loss during microneedle coating can be largely prevented through optimized formulation and that stabilized microneedle patches can be used for effective vaccination.