Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery

Latrisha K Petersen,1 Lucas Huntimer,2 Katharine Walz,1 Amanda Ramer-Tait,2 Michael J Wannemuehler,2 Balaji Narasimhan11Department of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA; 2Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames...

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Autores principales: Petersen LK, Huntimer L, Walz K, Ramer-Tait A, Wannemuehler MJ, Narasimhan B
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2013
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Acceso en línea:https://doaj.org/article/762970708cc744ec8fce550e3172651d
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Sumario:Latrisha K Petersen,1 Lucas Huntimer,2 Katharine Walz,1 Amanda Ramer-Tait,2 Michael J Wannemuehler,2 Balaji Narasimhan11Department of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA; 2Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA, USAAbstract: Several challenges are associated with current vaccine strategies, including repeated immunizations, poor patient compliance, and limited approved routes for delivery, which may hinder induction of protective immunity. Thus, there is a need for new vaccine adjuvants capable of multi-route administration and prolonged antigen release at the site of administration by providing a depot within tissue. In this work, we designed a combinatorial platform to investigate the in vivo distribution, depot effect, and localized persistence of polyanhydride nanoparticles as a function of nanoparticle chemistry and administration route. Our observations indicated that the route of administration differentially affected tissue residence times. All nanoparticles rapidly dispersed when delivered intranasally but provided a depot when administered parenterally. When amphiphilic and hydrophobic nanoparticles were administered intranasally, they persisted within lung tissue. These results provide insights into the chemistry- and route-dependent distribution and tissue-specific association of polyanhydride nanoparticle-based vaccine adjuvants.Keywords: combinatorial, polyanhydride, nanoparticle, live animal imaging, distribution