Freeze-Drying of Protein-Loaded Nanoparticles for Vaccine Delivery
Karishma Mody, Donna Mahony, Timothy J. Mahony and Neena Mitter
Pages 83-91 (9)
Conventional vaccines either use attenuated pathogens (live vaccines) or inactivated pathogens, such vaccines
can be expensive, difficult to deploy, require a ‘cold chain’, may have side effects and require multiple doses for effective
immunisation. Recent advances in the development of technology to delivery biologically active molecules in vivo have
utilised nanoparticles for the in vivo delivery of drugs, nucleic acids, proteins and peptides; nanotechnology has a promising
potential as a new platform technology for vaccine delivery. Nanoparticles allow controlled release of proteins and increase
the vaccine stability with the possibility of eliminating cold chain storage. Freeze-drying of protein-loaded
nanoparticles can be used to improve both the short and long-term stability of vaccine components. The purpose of this
review is to provide an overview of the freeze-drying process itself with the aim of identifying current procedures and parameters
that can impact the stability of the protein-loaded nanoparticles during and after freeze-drying. It also discusses
the formulation strategies, nanoparticle stability and the importance of excipients during the freeze-drying process. This
review will provide direction towards the successful integration of freeze-drying into the development of protein-based
nanovaccines to further enhance the application of this emerging vaccine technology platform.
Protein, antigen, nanoparticles, freeze-drying/lyophilisation, cryo/lyoprotectant, vaccine delivery.
Queensland Agricultural Biotechnology Facility, Ritchie Building No.64A, Research Road, The University of Queensland, St Lucia, Queensland Australia, 4072.