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Rotavirus-Like Particles: A Novel Nanocarrier for the Gut
The delivery of bioactive molecules directly to damaged tissues represents a technological challenge. We propose here a new system based on virus-like particles (VLP) from rotavirus, with a marked tropism for the gut to deliver bio-active molecules to intestinal cells. For this, nonreplicative VLP n...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856017/ https://www.ncbi.nlm.nih.gov/pubmed/20414353 http://dx.doi.org/10.1155/2010/317545 |
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author | Cortes-Perez, Naima G. Sapin, Catherine Jaffrelo, Loïc Daou, Sabine Grill, Jean Pierre Langella, Philippe Seksik, Philippe Beaugerie, Laurent Chwetzoff, Serge Trugnan, Germain |
author_facet | Cortes-Perez, Naima G. Sapin, Catherine Jaffrelo, Loïc Daou, Sabine Grill, Jean Pierre Langella, Philippe Seksik, Philippe Beaugerie, Laurent Chwetzoff, Serge Trugnan, Germain |
author_sort | Cortes-Perez, Naima G. |
collection | PubMed |
description | The delivery of bioactive molecules directly to damaged tissues represents a technological challenge. We propose here a new system based on virus-like particles (VLP) from rotavirus, with a marked tropism for the gut to deliver bio-active molecules to intestinal cells. For this, nonreplicative VLP nanoparticles were constructed using a baculovirus expression system and used to deliver an exogenous biomolecule, the green fluorescent protein (GFP), into either MA104 cells or intestinal cells from healthy and 2,4,6-trinitrobenzene sulfonic acid (TNBS)-treated mice. Our results show that expression of rotavirus capsid proteins in baculovirus led to the auto assembly of VLP that display similar properties to rotavirus. In vitro experiments showed that VLP were able to enter into MA104 cells and deliver the reporter protein. Intragastric administration of fluorescent VLP in healthy and TNBS-treated mice resulted in the detection of GFP and viral proteins in intestinal samples. Our results demonstrate an efficient entry of non-replicative rotavirus VLP into the epithelial cell line MA104 and provide the first in vivo evidence of the potential of these nanoparticles as a promising safe candidate for drug delivery to intestinal cells. |
format | Text |
id | pubmed-2856017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-28560172010-04-22 Rotavirus-Like Particles: A Novel Nanocarrier for the Gut Cortes-Perez, Naima G. Sapin, Catherine Jaffrelo, Loïc Daou, Sabine Grill, Jean Pierre Langella, Philippe Seksik, Philippe Beaugerie, Laurent Chwetzoff, Serge Trugnan, Germain J Biomed Biotechnol Research Article The delivery of bioactive molecules directly to damaged tissues represents a technological challenge. We propose here a new system based on virus-like particles (VLP) from rotavirus, with a marked tropism for the gut to deliver bio-active molecules to intestinal cells. For this, nonreplicative VLP nanoparticles were constructed using a baculovirus expression system and used to deliver an exogenous biomolecule, the green fluorescent protein (GFP), into either MA104 cells or intestinal cells from healthy and 2,4,6-trinitrobenzene sulfonic acid (TNBS)-treated mice. Our results show that expression of rotavirus capsid proteins in baculovirus led to the auto assembly of VLP that display similar properties to rotavirus. In vitro experiments showed that VLP were able to enter into MA104 cells and deliver the reporter protein. Intragastric administration of fluorescent VLP in healthy and TNBS-treated mice resulted in the detection of GFP and viral proteins in intestinal samples. Our results demonstrate an efficient entry of non-replicative rotavirus VLP into the epithelial cell line MA104 and provide the first in vivo evidence of the potential of these nanoparticles as a promising safe candidate for drug delivery to intestinal cells. Hindawi Publishing Corporation 2010 2010-04-13 /pmc/articles/PMC2856017/ /pubmed/20414353 http://dx.doi.org/10.1155/2010/317545 Text en Copyright © 2010 Naima G. Cortes-Perez et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cortes-Perez, Naima G. Sapin, Catherine Jaffrelo, Loïc Daou, Sabine Grill, Jean Pierre Langella, Philippe Seksik, Philippe Beaugerie, Laurent Chwetzoff, Serge Trugnan, Germain Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title | Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title_full | Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title_fullStr | Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title_full_unstemmed | Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title_short | Rotavirus-Like Particles: A Novel Nanocarrier for the Gut |
title_sort | rotavirus-like particles: a novel nanocarrier for the gut |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856017/ https://www.ncbi.nlm.nih.gov/pubmed/20414353 http://dx.doi.org/10.1155/2010/317545 |
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