Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles

Héctor L Rodríguez-Luccioni, Magda Latorre-Esteves, Janet Méndez-Vega, Orlando Soto, Ana R Rodríguez, Carlos Rinaldi, Madeline Torres-LugoDepartment of Chemical Engineering, University of Puerto Rico, Mayagüez 00681, Puerto Ric...

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Autores principales: Héctor L Rodríguez-Luccioni, Magda Latorre-Esteves, Janet Méndez-Vega, et al
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Publicado: Dove Medical Press 2011
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spelling oai:doaj.org-article:4853ef7deeef4f4f927a16bc6e2c514c2021-12-02T06:29:10ZEnhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles1176-91141178-2013https://doaj.org/article/4853ef7deeef4f4f927a16bc6e2c514c2011-02-01T00:00:00Zhttp://www.dovepress.com/enhanced-reduction-in-cell-viability-by-hyperthermia-induced-by-magnet-a6355https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Héctor L Rodríguez-Luccioni, Magda Latorre-Esteves, Janet Méndez-Vega, Orlando Soto, Ana R Rodríguez, Carlos Rinaldi, Madeline Torres-LugoDepartment of Chemical Engineering, University of Puerto Rico, Mayagüez 00681, Puerto RicoAbstract: Colloidal suspensions of iron oxide magnetic nanoparticles are known to dissipate energy when exposed to an oscillating magnetic field. Such energy dissipation can be employed to locally raise temperature inside a tumor between 41°C and 45°C (hyperthermia) to promote cell death, a treatment known as magnetic fluid hyperthermia (MFH). This work seeks to quantify differences between MFH and hot-water hyperthermia (HWH) in terms of reduction in cell viability using two cancer cell culture models, Caco-2 (human epithelial colorectal adenocarcinoma) and MCF-7 (human breast cancer). Magnetite nanoparticles were synthesized via the co-precipitation method and functionalized with adsorbed carboxymethyl dextran. Cytotoxicity studies indicated that in the absence of an oscillating magnetic field, cell viability was not affected at concentrations of up to 0.6 mg iron oxide/mL. MFH resulted in a significant decrease in cell viability when exposed to a magnetic field for 120 minutes and allowed to rest for 48 hours, compared with similar field applications, but with shorter resting time. The results presented here suggest that MFH most likely induces apoptosis in both cell types. When compared with HWH, MFH produced a significant reduction in cell viability, and these effects appear to be cell-type related.Keywords: magnetic fluid hyperthermia, carboxymethyl dextran magnetite, cell death, apoptosis Héctor L Rodríguez-LuccioniMagda Latorre-EstevesJanet Méndez-Vegaet alDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2011, Iss default, Pp 373-380 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Héctor L Rodríguez-Luccioni
Magda Latorre-Esteves
Janet Méndez-Vega
et al
Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
description Héctor L Rodríguez-Luccioni, Magda Latorre-Esteves, Janet Méndez-Vega, Orlando Soto, Ana R Rodríguez, Carlos Rinaldi, Madeline Torres-LugoDepartment of Chemical Engineering, University of Puerto Rico, Mayagüez 00681, Puerto RicoAbstract: Colloidal suspensions of iron oxide magnetic nanoparticles are known to dissipate energy when exposed to an oscillating magnetic field. Such energy dissipation can be employed to locally raise temperature inside a tumor between 41°C and 45°C (hyperthermia) to promote cell death, a treatment known as magnetic fluid hyperthermia (MFH). This work seeks to quantify differences between MFH and hot-water hyperthermia (HWH) in terms of reduction in cell viability using two cancer cell culture models, Caco-2 (human epithelial colorectal adenocarcinoma) and MCF-7 (human breast cancer). Magnetite nanoparticles were synthesized via the co-precipitation method and functionalized with adsorbed carboxymethyl dextran. Cytotoxicity studies indicated that in the absence of an oscillating magnetic field, cell viability was not affected at concentrations of up to 0.6 mg iron oxide/mL. MFH resulted in a significant decrease in cell viability when exposed to a magnetic field for 120 minutes and allowed to rest for 48 hours, compared with similar field applications, but with shorter resting time. The results presented here suggest that MFH most likely induces apoptosis in both cell types. When compared with HWH, MFH produced a significant reduction in cell viability, and these effects appear to be cell-type related.Keywords: magnetic fluid hyperthermia, carboxymethyl dextran magnetite, cell death, apoptosis
format article
author Héctor L Rodríguez-Luccioni
Magda Latorre-Esteves
Janet Méndez-Vega
et al
author_facet Héctor L Rodríguez-Luccioni
Magda Latorre-Esteves
Janet Méndez-Vega
et al
author_sort Héctor L Rodríguez-Luccioni
title Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
title_short Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
title_full Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
title_fullStr Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
title_full_unstemmed Enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
title_sort enhanced reduction in cell viability by hyperthermia induced by magnetic nanoparticles
publisher Dove Medical Press
publishDate 2011
url https://doaj.org/article/4853ef7deeef4f4f927a16bc6e2c514c
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AT magdalatorreesteves enhancedreductionincellviabilitybyhyperthermiainducedbymagneticnanoparticles
AT janetmampeacutendezvega enhancedreductionincellviabilitybyhyperthermiainducedbymagneticnanoparticles
AT etal enhancedreductionincellviabilitybyhyperthermiainducedbymagneticnanoparticles
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