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Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells

Even today, breast cancer remains a global public problem, with a high mortality rate among women. Nanoparticle (NP) based systems are developed to enhance drug delivery, reducing the toxic effect of medicine molecules. By using iron oxide nanoparticles for cancer treatment, several advantages were...

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Autores principales: Lungu, Iulia Ioana, Nistorescu, Simona, Badea, Mădălina Andreea, Petre, Andreea-Mihaela, Udrea, Ana-Maria, Banici, Ana-Maria, Fleacă, Claudiu, Andronescu, Ecaterina, Dinischiotu, Anca, Dumitrache, Florian, Staicu, Angela, Balaș, Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760716/
https://www.ncbi.nlm.nih.gov/pubmed/33256060
http://dx.doi.org/10.3390/polym12122799
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author Lungu, Iulia Ioana
Nistorescu, Simona
Badea, Mădălina Andreea
Petre, Andreea-Mihaela
Udrea, Ana-Maria
Banici, Ana-Maria
Fleacă, Claudiu
Andronescu, Ecaterina
Dinischiotu, Anca
Dumitrache, Florian
Staicu, Angela
Balaș, Mihaela
author_facet Lungu, Iulia Ioana
Nistorescu, Simona
Badea, Mădălina Andreea
Petre, Andreea-Mihaela
Udrea, Ana-Maria
Banici, Ana-Maria
Fleacă, Claudiu
Andronescu, Ecaterina
Dinischiotu, Anca
Dumitrache, Florian
Staicu, Angela
Balaș, Mihaela
author_sort Lungu, Iulia Ioana
collection PubMed
description Even today, breast cancer remains a global public problem, with a high mortality rate among women. Nanoparticle (NP) based systems are developed to enhance drug delivery, reducing the toxic effect of medicine molecules. By using iron oxide nanoparticles for cancer treatment, several advantages were highlighted: the ability to target specific locations derived from their magnetic properties and reduced side effects. The aim of this study was to examine on breast cancer cell line the anticancer potential of γ-Fe(2)O(3) NPs loaded with doxorubicin (DOX) and stabilized with carboxymethylcellulose sodium (CMCNa). The γ-Fe(2)O(3) NPs were synthesized by laser pyrolysis technique and their nanometric size and crystallinity were confirmed by X-ray diffraction and transmission electron microscopy. The loading efficiency was estimated by using absorption and fluorescence spectroscopy. The DOX conjugated//CMCNa coated γ-Fe(2)O(3) NPs proved through the biological studies to have a good anticancer effect through the inhibition of tumoral cell proliferation, disruption of the cellular membrane, induction of cell death and reduced effects on normal breast cells. Our data showed that DOX cytotoxicity increases significantly when conjugated with ɣ-Fe(2)O(3) and ɣ-Fe(2)O(3)_CMCNa, a 50% reduction of cancer cell viability was obtained with a concentration around 0.1 µg/mL.
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spelling pubmed-77607162020-12-26 Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells Lungu, Iulia Ioana Nistorescu, Simona Badea, Mădălina Andreea Petre, Andreea-Mihaela Udrea, Ana-Maria Banici, Ana-Maria Fleacă, Claudiu Andronescu, Ecaterina Dinischiotu, Anca Dumitrache, Florian Staicu, Angela Balaș, Mihaela Polymers (Basel) Article Even today, breast cancer remains a global public problem, with a high mortality rate among women. Nanoparticle (NP) based systems are developed to enhance drug delivery, reducing the toxic effect of medicine molecules. By using iron oxide nanoparticles for cancer treatment, several advantages were highlighted: the ability to target specific locations derived from their magnetic properties and reduced side effects. The aim of this study was to examine on breast cancer cell line the anticancer potential of γ-Fe(2)O(3) NPs loaded with doxorubicin (DOX) and stabilized with carboxymethylcellulose sodium (CMCNa). The γ-Fe(2)O(3) NPs were synthesized by laser pyrolysis technique and their nanometric size and crystallinity were confirmed by X-ray diffraction and transmission electron microscopy. The loading efficiency was estimated by using absorption and fluorescence spectroscopy. The DOX conjugated//CMCNa coated γ-Fe(2)O(3) NPs proved through the biological studies to have a good anticancer effect through the inhibition of tumoral cell proliferation, disruption of the cellular membrane, induction of cell death and reduced effects on normal breast cells. Our data showed that DOX cytotoxicity increases significantly when conjugated with ɣ-Fe(2)O(3) and ɣ-Fe(2)O(3)_CMCNa, a 50% reduction of cancer cell viability was obtained with a concentration around 0.1 µg/mL. MDPI 2020-11-26 /pmc/articles/PMC7760716/ /pubmed/33256060 http://dx.doi.org/10.3390/polym12122799 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
Lungu, Iulia Ioana
Nistorescu, Simona
Badea, Mădălina Andreea
Petre, Andreea-Mihaela
Udrea, Ana-Maria
Banici, Ana-Maria
Fleacă, Claudiu
Andronescu, Ecaterina
Dinischiotu, Anca
Dumitrache, Florian
Staicu, Angela
Balaș, Mihaela
Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title_full Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title_fullStr Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title_full_unstemmed Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title_short Doxorubicin-Conjugated Iron Oxide Nanoparticles Synthesized by Laser Pyrolysis: In Vitro Study on Human Breast Cancer Cells
title_sort doxorubicin-conjugated iron oxide nanoparticles synthesized by laser pyrolysis: in vitro study on human breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760716/
https://www.ncbi.nlm.nih.gov/pubmed/33256060
http://dx.doi.org/10.3390/polym12122799
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