Comparative manufacture and cell-based delivery of antiretroviral nanoformulations

Shantanu Balkundi1, Ari S Nowacek1, Ram S Veerubhotla1, Han Chen2, Andrea Martinez-Skinner1, Upal Roy1, R Lee Mosley1,3, Georgette Kanmogne1, Xinming Liu1,3,4, Alexander V Kabanov3,4, Tatiana Bronich3,4, JoEllyn McMillan1, Howard E Gendelman1,31Department of Pharmacology and Experimental Neuroscienc...

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Autores principales: Balkundi S, Nowacek AS, Veerubhotla RS, Chen H, Martinez-Skinner A, Roy U, Mosley RL, Kanmogne G, Liu X, Kabanov AV, Bronich T, McMillan J, Gendelman HE
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Publicado: Dove Medical Press 2011
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spelling oai:doaj.org-article:3116847039a74ce9ab92631e7e4f75622021-12-02T00:40:15ZComparative manufacture and cell-based delivery of antiretroviral nanoformulations1176-91141178-2013https://doaj.org/article/3116847039a74ce9ab92631e7e4f75622011-12-01T00:00:00Zhttp://www.dovepress.com/comparative-manufacture-and-cell-based-delivery-of-antiretroviral-nano-a8925https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Shantanu Balkundi1, Ari S Nowacek1, Ram S Veerubhotla1, Han Chen2, Andrea Martinez-Skinner1, Upal Roy1, R Lee Mosley1,3, Georgette Kanmogne1, Xinming Liu1,3,4, Alexander V Kabanov3,4, Tatiana Bronich3,4, JoEllyn McMillan1, Howard E Gendelman1,31Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA; 2Center for Biotechnology, University of Nebraska-Lincoln, Lincoln, NE, USA; 3Center for Drug Delivery and Nanomedicine, University of Nebraska Medical Center, Omaha, NE, USA; 4Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, USAAbstract: Nanoformulations of crystalline indinavir, ritonavir, atazanavir, and efavirenz were manufactured by wet milling, homogenization or sonication with a variety of excipients. The chemical, biological, immune, virological, and toxicological properties of these formulations were compared using an established monocyte-derived macrophage scoring indicator system. Measurements of drug uptake, retention, release, and antiretroviral activity demonstrated differences amongst preparation methods. Interestingly, for drug cell targeting and antiretroviral responses the most significant difference among the particles was the drug itself. We posit that the choice of drug and formulation composition may ultimately affect clinical utility.Keywords: human immunodeficiency virus type one, nanotoxicology, monocyte-derived macrophage, nanoformulated antiretroviral therapy, manufacturing techniquesBalkundi SNowacek ASVeerubhotla RSChen HMartinez-Skinner ARoy UMosley RLKanmogne GLiu XKabanov AVBronich TMcMillan JGendelman HEDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2011, Iss default, Pp 3393-3404 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Balkundi S
Nowacek AS
Veerubhotla RS
Chen H
Martinez-Skinner A
Roy U
Mosley RL
Kanmogne G
Liu X
Kabanov AV
Bronich T
McMillan J
Gendelman HE
Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
description Shantanu Balkundi1, Ari S Nowacek1, Ram S Veerubhotla1, Han Chen2, Andrea Martinez-Skinner1, Upal Roy1, R Lee Mosley1,3, Georgette Kanmogne1, Xinming Liu1,3,4, Alexander V Kabanov3,4, Tatiana Bronich3,4, JoEllyn McMillan1, Howard E Gendelman1,31Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA; 2Center for Biotechnology, University of Nebraska-Lincoln, Lincoln, NE, USA; 3Center for Drug Delivery and Nanomedicine, University of Nebraska Medical Center, Omaha, NE, USA; 4Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, USAAbstract: Nanoformulations of crystalline indinavir, ritonavir, atazanavir, and efavirenz were manufactured by wet milling, homogenization or sonication with a variety of excipients. The chemical, biological, immune, virological, and toxicological properties of these formulations were compared using an established monocyte-derived macrophage scoring indicator system. Measurements of drug uptake, retention, release, and antiretroviral activity demonstrated differences amongst preparation methods. Interestingly, for drug cell targeting and antiretroviral responses the most significant difference among the particles was the drug itself. We posit that the choice of drug and formulation composition may ultimately affect clinical utility.Keywords: human immunodeficiency virus type one, nanotoxicology, monocyte-derived macrophage, nanoformulated antiretroviral therapy, manufacturing techniques
format article
author Balkundi S
Nowacek AS
Veerubhotla RS
Chen H
Martinez-Skinner A
Roy U
Mosley RL
Kanmogne G
Liu X
Kabanov AV
Bronich T
McMillan J
Gendelman HE
author_facet Balkundi S
Nowacek AS
Veerubhotla RS
Chen H
Martinez-Skinner A
Roy U
Mosley RL
Kanmogne G
Liu X
Kabanov AV
Bronich T
McMillan J
Gendelman HE
author_sort Balkundi S
title Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
title_short Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
title_full Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
title_fullStr Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
title_full_unstemmed Comparative manufacture and cell-based delivery of antiretroviral nanoformulations
title_sort comparative manufacture and cell-based delivery of antiretroviral nanoformulations
publisher Dove Medical Press
publishDate 2011
url https://doaj.org/article/3116847039a74ce9ab92631e7e4f7562
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