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Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material

Gene therapy is a therapeutic process consisting of the transport of genetic material into cells. The design and preparation of novel carriers to transport DNA is an important research line in the medical field. Hybrid compounds such as metallo-liposomes, containing a mixture of lipids, were prepare...

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Autores principales: Lebrón, José Antonio, Ostos, Francisco José, López-López, Manuel, Moyá, María Luisa, Sales, Carlos, García, Encarnación, García-Calderón, Clara Beatriz, García-Calderón, Margarita, Peña-Gómez, María José, Rosado, Iván V., R. Balestra, Fernando, Huertas, Pablo, López-Cornejo, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284339/
https://www.ncbi.nlm.nih.gov/pubmed/32466339
http://dx.doi.org/10.3390/pharmaceutics12050482
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author Lebrón, José Antonio
Ostos, Francisco José
López-López, Manuel
Moyá, María Luisa
Sales, Carlos
García, Encarnación
García-Calderón, Clara Beatriz
García-Calderón, Margarita
Peña-Gómez, María José
Rosado, Iván V.
R. Balestra, Fernando
Huertas, Pablo
López-Cornejo, Pilar
author_facet Lebrón, José Antonio
Ostos, Francisco José
López-López, Manuel
Moyá, María Luisa
Sales, Carlos
García, Encarnación
García-Calderón, Clara Beatriz
García-Calderón, Margarita
Peña-Gómez, María José
Rosado, Iván V.
R. Balestra, Fernando
Huertas, Pablo
López-Cornejo, Pilar
author_sort Lebrón, José Antonio
collection PubMed
description Gene therapy is a therapeutic process consisting of the transport of genetic material into cells. The design and preparation of novel carriers to transport DNA is an important research line in the medical field. Hybrid compounds such as metallo-liposomes, containing a mixture of lipids, were prepared and characterized. Cationic metal lipids derived from the [Ru(bpy)(3)](2+) complex, RuC11C11 or RuC19C19, both with different hydrophobic/lipophilic ratios, were mixed with the phospholipid DOPE. A relation between the size and the molar fraction α was found and a multidisciplinary study about the interaction between the metallo-liposomes and DNA was performed. The metallo-liposomes/DNA association was quantified and a relationship between K(app) and α was obtained. Techniques such as AFM, SEM, zeta potential, dynamic light scattering and agarose gel electrophoresis demonstrated the formation of lipoplexes and showed the structure of the liposomes. L/D values corresponding to the polynucleotide’s condensation were estimated. In vitro assays proved the low cell toxicity of the metallo-liposomes, lower for normal cells than for cancer cell lines, and a good internalization into cells. The latter as well as the transfection measurements carried out with plasmid DNA pEGFP-C1 have demonstrated a good availability of the Ru(II)-based liposomes for being used as non-toxic nanovectors in gene therapy.
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spelling pubmed-72843392020-08-13 Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material Lebrón, José Antonio Ostos, Francisco José López-López, Manuel Moyá, María Luisa Sales, Carlos García, Encarnación García-Calderón, Clara Beatriz García-Calderón, Margarita Peña-Gómez, María José Rosado, Iván V. R. Balestra, Fernando Huertas, Pablo López-Cornejo, Pilar Pharmaceutics Article Gene therapy is a therapeutic process consisting of the transport of genetic material into cells. The design and preparation of novel carriers to transport DNA is an important research line in the medical field. Hybrid compounds such as metallo-liposomes, containing a mixture of lipids, were prepared and characterized. Cationic metal lipids derived from the [Ru(bpy)(3)](2+) complex, RuC11C11 or RuC19C19, both with different hydrophobic/lipophilic ratios, were mixed with the phospholipid DOPE. A relation between the size and the molar fraction α was found and a multidisciplinary study about the interaction between the metallo-liposomes and DNA was performed. The metallo-liposomes/DNA association was quantified and a relationship between K(app) and α was obtained. Techniques such as AFM, SEM, zeta potential, dynamic light scattering and agarose gel electrophoresis demonstrated the formation of lipoplexes and showed the structure of the liposomes. L/D values corresponding to the polynucleotide’s condensation were estimated. In vitro assays proved the low cell toxicity of the metallo-liposomes, lower for normal cells than for cancer cell lines, and a good internalization into cells. The latter as well as the transfection measurements carried out with plasmid DNA pEGFP-C1 have demonstrated a good availability of the Ru(II)-based liposomes for being used as non-toxic nanovectors in gene therapy. MDPI 2020-05-25 /pmc/articles/PMC7284339/ /pubmed/32466339 http://dx.doi.org/10.3390/pharmaceutics12050482 Text en © 2020 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
Lebrón, José Antonio
Ostos, Francisco José
López-López, Manuel
Moyá, María Luisa
Sales, Carlos
García, Encarnación
García-Calderón, Clara Beatriz
García-Calderón, Margarita
Peña-Gómez, María José
Rosado, Iván V.
R. Balestra, Fernando
Huertas, Pablo
López-Cornejo, Pilar
Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title_full Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title_fullStr Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title_full_unstemmed Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title_short Metallo-Liposomes of Ruthenium Used as Promising Vectors of Genetic Material
title_sort metallo-liposomes of ruthenium used as promising vectors of genetic material
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284339/
https://www.ncbi.nlm.nih.gov/pubmed/32466339
http://dx.doi.org/10.3390/pharmaceutics12050482
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