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Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous del...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922173/ https://www.ncbi.nlm.nih.gov/pubmed/33669785 http://dx.doi.org/10.3390/pharmaceutics13020281 |
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author | Sanmartín, Isaías Sendra, Luis Moret, Inés Herrero, María José Aliño, Salvador F. |
author_facet | Sanmartín, Isaías Sendra, Luis Moret, Inés Herrero, María José Aliño, Salvador F. |
author_sort | Sanmartín, Isaías |
collection | PubMed |
description | Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous delivery of lipid or water-soluble antigens associated with genes to the same cell, in much higher amounts than conventional lipopolyplexes. The vector characterization and optimization were carried out using liposomes with entrapped carboxyfluorescein and adapted electrophoretic assays. Two types of lipopolyplexes (containing hydrophilic or lipophilic antigens) were employed to evaluate their interest in vaccination. The lipopolyplex loaded with an extract of water-soluble melanoma proteins proved to efficiently induce humoral response in murine melanoma model, increasing the levels of IgM and IgG. The specificity of the immune response induced by the lipopolyplex was demonstrated in mice with the lipopolyplex containing the GD3 ganglioside lipid antigen, abundant in melanoma cells. The levels of anti-GD3 IgG increased markedly without modifying the expression of humoral antibodies against other gangliosides. |
format | Online Article Text |
id | pubmed-7922173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79221732021-03-03 Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations Sanmartín, Isaías Sendra, Luis Moret, Inés Herrero, María José Aliño, Salvador F. Pharmaceutics Article Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous delivery of lipid or water-soluble antigens associated with genes to the same cell, in much higher amounts than conventional lipopolyplexes. The vector characterization and optimization were carried out using liposomes with entrapped carboxyfluorescein and adapted electrophoretic assays. Two types of lipopolyplexes (containing hydrophilic or lipophilic antigens) were employed to evaluate their interest in vaccination. The lipopolyplex loaded with an extract of water-soluble melanoma proteins proved to efficiently induce humoral response in murine melanoma model, increasing the levels of IgM and IgG. The specificity of the immune response induced by the lipopolyplex was demonstrated in mice with the lipopolyplex containing the GD3 ganglioside lipid antigen, abundant in melanoma cells. The levels of anti-GD3 IgG increased markedly without modifying the expression of humoral antibodies against other gangliosides. MDPI 2021-02-19 /pmc/articles/PMC7922173/ /pubmed/33669785 http://dx.doi.org/10.3390/pharmaceutics13020281 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sanmartín, Isaías Sendra, Luis Moret, Inés Herrero, María José Aliño, Salvador F. Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title | Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title_full | Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title_fullStr | Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title_full_unstemmed | Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title_short | Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations |
title_sort | multicompartmental lipopolyplex as vehicle for antigens and genes delivery in vaccine formulations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922173/ https://www.ncbi.nlm.nih.gov/pubmed/33669785 http://dx.doi.org/10.3390/pharmaceutics13020281 |
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