Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles
- Autores
- Ferronato, María Julia; Facchinetti, Maria Marta; Curino, Alejandro Carlos; Agotegaray, Mariela Alejandra; Lasalle, María de Las Nieves
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- INTRODUCTION. Magnetic nanoparticles (MNPs) represent a tool for localized therapeutics on specific sites of the body by the influence of an external magnetic field. They may act as drug carriers as well as contrast agents for resonance magnetic images and agents for hyperthermia treatment in different oncological pathologies. In this work, we developed MNPs coated with different agents in order to induce biocompatible platforms for future loading of chemotherapies. Their effects on cell viability of murine triple negative breast cancer cells (TNBC) were studied to provide novel information for possible future clinical applications.MATERIALS AND METHODS: MNPs were synthesized by co-precipitation method from iron precursors and different coating agents: citric acid, glutamic acid, adenine, oleic acid, beta-cyclodextrin, and 3-aminopropyltriethoxysilane (APTES). Physicochemical characterization was performed employing FTIR spectroscopy, analysis of hydrodynamic diameter and zeta potential, transmission electronic microscopy and iron content. Cell viability of murine 4T1TNBC cells exposed for 24 h to different concentrations of MNPs (0-500 μg/mL) was evaluated by crystal violet staining assays. The experiments were repeated twice and performed in triplicate.RESULTS. Spectroscopic studies demonstrated the successful coating of the different MNPs with the coating agents employed. Physicochemical properties of MNPs were proper for biomedical applications in terms of hydrodynamic diameters (between 200 and 350 nm) and stability in physiological media pH near 7 (PDI<0.5). No differences were found on TNBC cell viability between nano-formulations or control cells at any of the concentrations tested. CONCLUSION. The MNPs studied with different biocompatible coating agents did not alter viability of murine TNBC cells by themselves. In this way, these MNPs may be used as platform for loading of different drugs intended to improve breast cancer current therapies.
Fil: Ferronato, María Julia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Facchinetti, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Curino, Alejandro Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Agotegaray, Mariela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Fil: Lasalle, María de Las Nieves. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
1st zooming into preclinical Nanomedicines in the era Covid-19
Argentina
La Asociación Argentina de Nanomedicinas - Materia
-
MAGNETIC
NANOPARTICLES
BREAST CANCER
TRIPLE NEGATIVE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/199925
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Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticlesFerronato, María JuliaFacchinetti, Maria MartaCurino, Alejandro CarlosAgotegaray, Mariela AlejandraLasalle, María de Las NievesMAGNETICNANOPARTICLESBREAST CANCERTRIPLE NEGATIVEhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3INTRODUCTION. Magnetic nanoparticles (MNPs) represent a tool for localized therapeutics on specific sites of the body by the influence of an external magnetic field. They may act as drug carriers as well as contrast agents for resonance magnetic images and agents for hyperthermia treatment in different oncological pathologies. In this work, we developed MNPs coated with different agents in order to induce biocompatible platforms for future loading of chemotherapies. Their effects on cell viability of murine triple negative breast cancer cells (TNBC) were studied to provide novel information for possible future clinical applications.MATERIALS AND METHODS: MNPs were synthesized by co-precipitation method from iron precursors and different coating agents: citric acid, glutamic acid, adenine, oleic acid, beta-cyclodextrin, and 3-aminopropyltriethoxysilane (APTES). Physicochemical characterization was performed employing FTIR spectroscopy, analysis of hydrodynamic diameter and zeta potential, transmission electronic microscopy and iron content. Cell viability of murine 4T1TNBC cells exposed for 24 h to different concentrations of MNPs (0-500 μg/mL) was evaluated by crystal violet staining assays. The experiments were repeated twice and performed in triplicate.RESULTS. Spectroscopic studies demonstrated the successful coating of the different MNPs with the coating agents employed. Physicochemical properties of MNPs were proper for biomedical applications in terms of hydrodynamic diameters (between 200 and 350 nm) and stability in physiological media pH near 7 (PDI<0.5). No differences were found on TNBC cell viability between nano-formulations or control cells at any of the concentrations tested. CONCLUSION. The MNPs studied with different biocompatible coating agents did not alter viability of murine TNBC cells by themselves. In this way, these MNPs may be used as platform for loading of different drugs intended to improve breast cancer current therapies.Fil: Ferronato, María Julia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Facchinetti, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Curino, Alejandro Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Agotegaray, Mariela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; ArgentinaFil: Lasalle, María de Las Nieves. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina1st zooming into preclinical Nanomedicines in the era Covid-19ArgentinaLa Asociación Argentina de NanomedicinasAsociación Argentina de Nanomedicinas, NanomedAR2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectConferenciaJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/199925Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles; 1st zooming into preclinical Nanomedicines in the era Covid-19; Argentina; 2020; 26-272718-7098CONICET DigitalCONICETengInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:06:37Zoai:ri.conicet.gov.ar:11336/199925instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:06:37.424CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
title |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
spellingShingle |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles Ferronato, María Julia MAGNETIC NANOPARTICLES BREAST CANCER TRIPLE NEGATIVE |
title_short |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
title_full |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
title_fullStr |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
title_full_unstemmed |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
title_sort |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles |
dc.creator.none.fl_str_mv |
Ferronato, María Julia Facchinetti, Maria Marta Curino, Alejandro Carlos Agotegaray, Mariela Alejandra Lasalle, María de Las Nieves |
author |
Ferronato, María Julia |
author_facet |
Ferronato, María Julia Facchinetti, Maria Marta Curino, Alejandro Carlos Agotegaray, Mariela Alejandra Lasalle, María de Las Nieves |
author_role |
author |
author2 |
Facchinetti, Maria Marta Curino, Alejandro Carlos Agotegaray, Mariela Alejandra Lasalle, María de Las Nieves |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
MAGNETIC NANOPARTICLES BREAST CANCER TRIPLE NEGATIVE |
topic |
MAGNETIC NANOPARTICLES BREAST CANCER TRIPLE NEGATIVE |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
INTRODUCTION. Magnetic nanoparticles (MNPs) represent a tool for localized therapeutics on specific sites of the body by the influence of an external magnetic field. They may act as drug carriers as well as contrast agents for resonance magnetic images and agents for hyperthermia treatment in different oncological pathologies. In this work, we developed MNPs coated with different agents in order to induce biocompatible platforms for future loading of chemotherapies. Their effects on cell viability of murine triple negative breast cancer cells (TNBC) were studied to provide novel information for possible future clinical applications.MATERIALS AND METHODS: MNPs were synthesized by co-precipitation method from iron precursors and different coating agents: citric acid, glutamic acid, adenine, oleic acid, beta-cyclodextrin, and 3-aminopropyltriethoxysilane (APTES). Physicochemical characterization was performed employing FTIR spectroscopy, analysis of hydrodynamic diameter and zeta potential, transmission electronic microscopy and iron content. Cell viability of murine 4T1TNBC cells exposed for 24 h to different concentrations of MNPs (0-500 μg/mL) was evaluated by crystal violet staining assays. The experiments were repeated twice and performed in triplicate.RESULTS. Spectroscopic studies demonstrated the successful coating of the different MNPs with the coating agents employed. Physicochemical properties of MNPs were proper for biomedical applications in terms of hydrodynamic diameters (between 200 and 350 nm) and stability in physiological media pH near 7 (PDI<0.5). No differences were found on TNBC cell viability between nano-formulations or control cells at any of the concentrations tested. CONCLUSION. The MNPs studied with different biocompatible coating agents did not alter viability of murine TNBC cells by themselves. In this way, these MNPs may be used as platform for loading of different drugs intended to improve breast cancer current therapies. Fil: Ferronato, María Julia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Facchinetti, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Curino, Alejandro Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Agotegaray, Mariela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina Fil: Lasalle, María de Las Nieves. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina 1st zooming into preclinical Nanomedicines in the era Covid-19 Argentina La Asociación Argentina de Nanomedicinas |
description |
INTRODUCTION. Magnetic nanoparticles (MNPs) represent a tool for localized therapeutics on specific sites of the body by the influence of an external magnetic field. They may act as drug carriers as well as contrast agents for resonance magnetic images and agents for hyperthermia treatment in different oncological pathologies. In this work, we developed MNPs coated with different agents in order to induce biocompatible platforms for future loading of chemotherapies. Their effects on cell viability of murine triple negative breast cancer cells (TNBC) were studied to provide novel information for possible future clinical applications.MATERIALS AND METHODS: MNPs were synthesized by co-precipitation method from iron precursors and different coating agents: citric acid, glutamic acid, adenine, oleic acid, beta-cyclodextrin, and 3-aminopropyltriethoxysilane (APTES). Physicochemical characterization was performed employing FTIR spectroscopy, analysis of hydrodynamic diameter and zeta potential, transmission electronic microscopy and iron content. Cell viability of murine 4T1TNBC cells exposed for 24 h to different concentrations of MNPs (0-500 μg/mL) was evaluated by crystal violet staining assays. The experiments were repeated twice and performed in triplicate.RESULTS. Spectroscopic studies demonstrated the successful coating of the different MNPs with the coating agents employed. Physicochemical properties of MNPs were proper for biomedical applications in terms of hydrodynamic diameters (between 200 and 350 nm) and stability in physiological media pH near 7 (PDI<0.5). No differences were found on TNBC cell viability between nano-formulations or control cells at any of the concentrations tested. CONCLUSION. The MNPs studied with different biocompatible coating agents did not alter viability of murine TNBC cells by themselves. In this way, these MNPs may be used as platform for loading of different drugs intended to improve breast cancer current therapies. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Conferencia Journal http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/199925 Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles; 1st zooming into preclinical Nanomedicines in the era Covid-19; Argentina; 2020; 26-27 2718-7098 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/199925 |
identifier_str_mv |
Evaluation of murine triple negative breast cancer cell viability exposed to magnetic nanoparticles; 1st zooming into preclinical Nanomedicines in the era Covid-19; Argentina; 2020; 26-27 2718-7098 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf application/pdf |
dc.coverage.none.fl_str_mv |
Internacional |
dc.publisher.none.fl_str_mv |
Asociación Argentina de Nanomedicinas, NanomedAR |
publisher.none.fl_str_mv |
Asociación Argentina de Nanomedicinas, NanomedAR |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |