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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Dove Medical Press
2013
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oai:doaj.org-article:762970708cc744ec8fce550e3172651d2021-12-02T00:43:05ZCombinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery1176-91141178-2013https://doaj.org/article/762970708cc744ec8fce550e3172651d2013-06-01T00:00:00Zhttp://www.dovepress.com/combinatorial-evaluation-of-in-vivo-distribution-of-polyanhydride-part-a13389https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Latrisha 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, distributionPetersen LKHuntimer LWalz KRamer-Tait AWannemuehler MJNarasimhan BDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2013, Iss default, Pp 2213-2225 (2013) |
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Medicine (General) R5-920 |
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Medicine (General) R5-920 Petersen LK Huntimer L Walz K Ramer-Tait A Wannemuehler MJ Narasimhan B Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
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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 |
format |
article |
author |
Petersen LK Huntimer L Walz K Ramer-Tait A Wannemuehler MJ Narasimhan B |
author_facet |
Petersen LK Huntimer L Walz K Ramer-Tait A Wannemuehler MJ Narasimhan B |
author_sort |
Petersen LK |
title |
Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
title_short |
Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
title_full |
Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
title_fullStr |
Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
title_full_unstemmed |
Combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
title_sort |
combinatorial evaluation of in vivo distribution of polyanhydride particle-based platforms for vaccine delivery |
publisher |
Dove Medical Press |
publishDate |
2013 |
url |
https://doaj.org/article/762970708cc744ec8fce550e3172651d |
work_keys_str_mv |
AT petersenlk combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery AT huntimerl combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery AT walzk combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery AT ramertaita combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery AT wannemuehlermj combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery AT narasimhanb combinatorialevaluationofinvivodistributionofpolyanhydrideparticlebasedplatformsforvaccinedelivery |
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1718403505124802560 |