Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents

The obtaining of nanocarriers of gene material and small drugs is still an interesting research line. Side-effects produced by the toxicity of several pharmaceutics, the high concentrations needed to get therapeutic effects, or their excessive use by patients have motivated the search for new nanost...

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Main Authors: Maria Luisa Moyá, Francisco José Ostos, Izamar Moreno, Diandra García, Paula Moreno-Gordillo, Ivan V. Rosado, Pilar López-Cornejo, José Antonio Lebrón, Manuel López-López
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Chemosensors
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Online Access:https://www.mdpi.com/2227-9040/9/5/90
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author Maria Luisa Moyá
Francisco José Ostos
Izamar Moreno
Diandra García
Paula Moreno-Gordillo
Ivan V. Rosado
Pilar López-Cornejo
José Antonio Lebrón
Manuel López-López
author_facet Maria Luisa Moyá
Francisco José Ostos
Izamar Moreno
Diandra García
Paula Moreno-Gordillo
Ivan V. Rosado
Pilar López-Cornejo
José Antonio Lebrón
Manuel López-López
author_sort Maria Luisa Moyá
collection DOAJ
description The obtaining of nanocarriers of gene material and small drugs is still an interesting research line. Side-effects produced by the toxicity of several pharmaceutics, the high concentrations needed to get therapeutic effects, or their excessive use by patients have motivated the search for new nanostructures. For these reasons, cationic metallo-liposomes composed by phosphatidylcholine (PC), cholesterol (CHO) and RuC1C19 (a surfactant derived from the metallic complex [Ru(bpy)<sub>3</sub>]<sup>2+</sup>) were prepared and characterized by using diverse techniques (zeta potential, dynamic light scattering and electronic transmission microscopy –TEM-). Unimodal or bimodal populations of spherical aggregates with small sizes were obtained depending on the composition of the liposomes. The presence of cholesterol favored the formation of small aggregates. ct-DNA was condensed in the presence of the liposomes investigated. In-vitro assays demonstrated the ability of these nanoaggregates to internalize into different cell lines. A positive gene transfection into human bone osteosarcoma epithelial cells (U2OS) was also observed. The RuC1C19 surfactant was used as sensor to quantify the binding of DNA to the liposomes. Doxorubicin was encapsulated into the metallo-liposomes, demonstrating their ability to be also used as nanocarriers of drugs. A relationship between then encapsulation percentage of the antibiotic and the composition of the aggregates has been established.
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spelling doaj.art-b4b827e5bbda4f949b9c018372c12cff2023-11-21T17:07:32ZengMDPI AGChemosensors2227-90402021-04-01959010.3390/chemosensors9050090Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic AgentsMaria Luisa Moyá0Francisco José Ostos1Izamar Moreno2Diandra García3Paula Moreno-Gordillo4Ivan V. Rosado5Pilar López-Cornejo6José Antonio Lebrón7Manuel López-López8Department of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainDepartment of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainDepartment of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainDepartment of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainInstitute of Biomedicine of Seville (IBiS), University Hospital Virgen del Rocio/CSIC/University of Seville, Avda. Manuel Siurot s/n, 41013 Seville, SpainInstitute of Biomedicine of Seville (IBiS), University Hospital Virgen del Rocio/CSIC/University of Seville, Avda. Manuel Siurot s/n, 41013 Seville, SpainDepartment of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainDepartment of Physical Chemistry, Faculty of Chemistry, University of Seville, C/Professor García González 1, 41012 Seville, SpainDepartment of Chemical Engineering, Physical Chemistry and Materials Science, Faculty of Experimental Sciences, Campus de El Carmen, Avda. de las Fuerzas Armadas s/n, 21071 Huelva, SpainThe obtaining of nanocarriers of gene material and small drugs is still an interesting research line. Side-effects produced by the toxicity of several pharmaceutics, the high concentrations needed to get therapeutic effects, or their excessive use by patients have motivated the search for new nanostructures. For these reasons, cationic metallo-liposomes composed by phosphatidylcholine (PC), cholesterol (CHO) and RuC1C19 (a surfactant derived from the metallic complex [Ru(bpy)<sub>3</sub>]<sup>2+</sup>) were prepared and characterized by using diverse techniques (zeta potential, dynamic light scattering and electronic transmission microscopy –TEM-). Unimodal or bimodal populations of spherical aggregates with small sizes were obtained depending on the composition of the liposomes. The presence of cholesterol favored the formation of small aggregates. ct-DNA was condensed in the presence of the liposomes investigated. In-vitro assays demonstrated the ability of these nanoaggregates to internalize into different cell lines. A positive gene transfection into human bone osteosarcoma epithelial cells (U2OS) was also observed. The RuC1C19 surfactant was used as sensor to quantify the binding of DNA to the liposomes. Doxorubicin was encapsulated into the metallo-liposomes, demonstrating their ability to be also used as nanocarriers of drugs. A relationship between then encapsulation percentage of the antibiotic and the composition of the aggregates has been established.https://www.mdpi.com/2227-9040/9/5/90metallo-liposomenanocarriergene therapyDNAdoxorubicinTEM
spellingShingle Maria Luisa Moyá
Francisco José Ostos
Izamar Moreno
Diandra García
Paula Moreno-Gordillo
Ivan V. Rosado
Pilar López-Cornejo
José Antonio Lebrón
Manuel López-López
Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
Chemosensors
metallo-liposome
nanocarrier
gene therapy
DNA
doxorubicin
TEM
title Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
title_full Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
title_fullStr Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
title_full_unstemmed Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
title_short Metallo-Liposomes Derived from the [Ru(bpy)<sub>3</sub>]<sup>2+</sup> Complex as Nanocarriers of Therapeutic Agents
title_sort metallo liposomes derived from the ru bpy sub 3 sub sup 2 sup complex as nanocarriers of therapeutic agents
topic metallo-liposome
nanocarrier
gene therapy
DNA
doxorubicin
TEM
url https://www.mdpi.com/2227-9040/9/5/90
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