Affiliations: Delivery of Drugs and Genes Group (D2G2), Australian
Institute for Bioengineering and Nanotechnology, The University of Queensland,
Brisbane, QLD, Australia
Note: [] Correspondence: Professor Mark Kendall, The University of
Queensland, Delivery of Drugs and Genes Group (D2G2), Australian Institute for
Bioengineering and Nanotechnology, Brisbane, QLD 4072, Australia. Tel.: +61 7
334 64265; E-mail: m.kendall@ug.edu.au
Abstract: Young children are of the highest hospital admission rate of all
influenza cases. A broad and effective rollout of influenza vaccines for
children is hindered by the current most common method of administration: the
needle and syringe. Limitations include: reduced compliance due to
needle-phobia; increased costs due to maintaining refrigeration due to
transportation and storage (the "cold chain"); the need for qualified
medical/nursing practitioners – to help reduce risk of unsafe injections
and needle-stick injuries; and potentially impeded immunity – by delivery
to muscle and not accessing the abundant antigen presenting cell populations
resident in skin and mucosal surfaces. This paper explores needle-free routes
to improved childhood influenza vaccines rollout, by being a practical device
for self-administration that has also generated significantly-improved
immunogenicity and also the removal of the cold chain (through
dry-formulation). Marketed devices targeting the mucosa through intranasal
delivery (of liquid vaccine) are analysed, together with skin-targeting
approaches currently in development – offering both improved
immunogenicity and cold-chain removal by formulating the vaccine in a solid
form.