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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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Detalles Bibliográficos
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
Descripción
Sumario: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.