In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats

Detalhes bibliográficos
Autor(a) principal: Pereira, Vitor H.
Data de Publicação: 2011
Outros Autores: Salgado, A. J., Oliveira, Joaquim M., Cerqueira, Susana R., Frias, A. M., Fraga, J. S., Roque, Susana, Falcão, Ana M., Marques, Fernanda Cristina Gomes de Sousa, Neves, N. M., Mano, J. F., Reis, R. L., Sousa, Nuno
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/16935
Resumo: Carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles (CMCht/PAMAM) have recently been proposed for intracellular drug delivery purposes. These are constituted by a PAMAM dendrimer core grafted with chains of CMCht. Previous reports have shown that these nanoparticles disclosed an improved cytotoxic profile when compared to traditional dendrimers. Following on these results the present study aims to assess, for the first time, the short-term in vivo biodistribution of CMCht/PAMAM dendrimer nanoparticles upon intravenous injections in Wistar Han rats. The rats were injected in the tail vein with 1 and 10 µg/g, respectively, of fluorescein isothiocyanate (FITC) labeled CMCht/PAMAM dendrimer nanoparticles. Brain, liver, kidney and lung were collected at 24, 48 and 72 hours after injection and further stained with phalloidin-TRITC (red) and DAPI (blue) to trace the nanoparticles within the tissues. Liver, kidney and lung were also stained for haematoxylin and eosin in order to assess possible alterations in the morphology of these organs. CMCht/PAMAM dendrimer nanoparticles were observed within the vascular space and parenchyma of liver, kidney and lung, and in the choroid plexus, after 24, 48 and 72 hours upon intravenous injection of nanoparticles. No particles were observed in the brain parenchyma, nor any apparent deleterious histological changes, were observed within these organs. The present report revealed that CMCht/PAMAM dendrimer nanoparticles were stable in circulation for periods up to 72 hours, targeting the main organs/systems through internalization by the cells present in their parenchyma. These results provide positive indicators to their potential use in the future as intracellular drug delivery systems.
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spelling In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in ratsIn vivoPoly(amidoamine) dendrimersCarboxymethylchitosanBiodistributionFluorescenceCentral nervous systemDendrimer nanoparticlesIntracellular nanoparticlesDrug delivery systemsScience & TechnologyCarboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles (CMCht/PAMAM) have recently been proposed for intracellular drug delivery purposes. These are constituted by a PAMAM dendrimer core grafted with chains of CMCht. Previous reports have shown that these nanoparticles disclosed an improved cytotoxic profile when compared to traditional dendrimers. Following on these results the present study aims to assess, for the first time, the short-term in vivo biodistribution of CMCht/PAMAM dendrimer nanoparticles upon intravenous injections in Wistar Han rats. The rats were injected in the tail vein with 1 and 10 µg/g, respectively, of fluorescein isothiocyanate (FITC) labeled CMCht/PAMAM dendrimer nanoparticles. Brain, liver, kidney and lung were collected at 24, 48 and 72 hours after injection and further stained with phalloidin-TRITC (red) and DAPI (blue) to trace the nanoparticles within the tissues. Liver, kidney and lung were also stained for haematoxylin and eosin in order to assess possible alterations in the morphology of these organs. CMCht/PAMAM dendrimer nanoparticles were observed within the vascular space and parenchyma of liver, kidney and lung, and in the choroid plexus, after 24, 48 and 72 hours upon intravenous injection of nanoparticles. No particles were observed in the brain parenchyma, nor any apparent deleterious histological changes, were observed within these organs. The present report revealed that CMCht/PAMAM dendrimer nanoparticles were stable in circulation for periods up to 72 hours, targeting the main organs/systems through internalization by the cells present in their parenchyma. These results provide positive indicators to their potential use in the future as intracellular drug delivery systems.Funds attributed by Fundação Calouste de Gulbenkian to A.J. Salgado under the scope of the The Gulbenkian Programme to Support Research in Life Sciences; Portuguese Foundation for Science and Technology (Science 2007 Program – A.J. Salgado, pre- and postdoctoral fellowships to J.M. Oliveira – SFRH/BPD/63175/2009, A.M. Frias – SFRH/BPD/45206/2008, F. Marques – SFRH/BPD/33379/2008, A.M. Falcão – SFRH/BD/44485/2008, S. Roque – SFRH/BD/24539/2005; S.R. Cerqueira – SFRH/BD/SFRH/BD/48406: 2008).SAGEUniversidade do MinhoPereira, Vitor H.Salgado, A. J.Oliveira, Joaquim M.Cerqueira, Susana R.Frias, A. M.Fraga, J. S.Roque, SusanaFalcão, Ana M.Marques, Fernanda Cristina Gomes de SousaNeves, N. M.Mano, J. F.Reis, R. L.Sousa, Nuno20112011-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/16935eng0883-911510.1177/0883911511425567http://dx.doi.org/10.1177/0883911511425567info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:54:36Zoai:repositorium.sdum.uminho.pt:1822/16935Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:54:12.425540Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
title In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
spellingShingle In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
Pereira, Vitor H.
In vivo
Poly(amidoamine) dendrimers
Carboxymethylchitosan
Biodistribution
Fluorescence
Central nervous system
Dendrimer nanoparticles
Intracellular nanoparticles
Drug delivery systems
Science & Technology
title_short In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
title_full In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
title_fullStr In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
title_full_unstemmed In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
title_sort In vivo biodistribution of carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles in rats
author Pereira, Vitor H.
author_facet Pereira, Vitor H.
Salgado, A. J.
Oliveira, Joaquim M.
Cerqueira, Susana R.
Frias, A. M.
Fraga, J. S.
Roque, Susana
Falcão, Ana M.
Marques, Fernanda Cristina Gomes de Sousa
Neves, N. M.
Mano, J. F.
Reis, R. L.
Sousa, Nuno
author_role author
author2 Salgado, A. J.
Oliveira, Joaquim M.
Cerqueira, Susana R.
Frias, A. M.
Fraga, J. S.
Roque, Susana
Falcão, Ana M.
Marques, Fernanda Cristina Gomes de Sousa
Neves, N. M.
Mano, J. F.
Reis, R. L.
Sousa, Nuno
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Pereira, Vitor H.
Salgado, A. J.
Oliveira, Joaquim M.
Cerqueira, Susana R.
Frias, A. M.
Fraga, J. S.
Roque, Susana
Falcão, Ana M.
Marques, Fernanda Cristina Gomes de Sousa
Neves, N. M.
Mano, J. F.
Reis, R. L.
Sousa, Nuno
dc.subject.por.fl_str_mv In vivo
Poly(amidoamine) dendrimers
Carboxymethylchitosan
Biodistribution
Fluorescence
Central nervous system
Dendrimer nanoparticles
Intracellular nanoparticles
Drug delivery systems
Science & Technology
topic In vivo
Poly(amidoamine) dendrimers
Carboxymethylchitosan
Biodistribution
Fluorescence
Central nervous system
Dendrimer nanoparticles
Intracellular nanoparticles
Drug delivery systems
Science & Technology
description Carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles (CMCht/PAMAM) have recently been proposed for intracellular drug delivery purposes. These are constituted by a PAMAM dendrimer core grafted with chains of CMCht. Previous reports have shown that these nanoparticles disclosed an improved cytotoxic profile when compared to traditional dendrimers. Following on these results the present study aims to assess, for the first time, the short-term in vivo biodistribution of CMCht/PAMAM dendrimer nanoparticles upon intravenous injections in Wistar Han rats. The rats were injected in the tail vein with 1 and 10 µg/g, respectively, of fluorescein isothiocyanate (FITC) labeled CMCht/PAMAM dendrimer nanoparticles. Brain, liver, kidney and lung were collected at 24, 48 and 72 hours after injection and further stained with phalloidin-TRITC (red) and DAPI (blue) to trace the nanoparticles within the tissues. Liver, kidney and lung were also stained for haematoxylin and eosin in order to assess possible alterations in the morphology of these organs. CMCht/PAMAM dendrimer nanoparticles were observed within the vascular space and parenchyma of liver, kidney and lung, and in the choroid plexus, after 24, 48 and 72 hours upon intravenous injection of nanoparticles. No particles were observed in the brain parenchyma, nor any apparent deleterious histological changes, were observed within these organs. The present report revealed that CMCht/PAMAM dendrimer nanoparticles were stable in circulation for periods up to 72 hours, targeting the main organs/systems through internalization by the cells present in their parenchyma. These results provide positive indicators to their potential use in the future as intracellular drug delivery systems.
publishDate 2011
dc.date.none.fl_str_mv 2011
2011-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/16935
url http://hdl.handle.net/1822/16935
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0883-9115
10.1177/0883911511425567
http://dx.doi.org/10.1177/0883911511425567
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv SAGE
publisher.none.fl_str_mv SAGE
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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