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The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment

Herein, the authors synthesised chitosan nanoparticles (Cs NPs) as a resveratrol (RSV) carrier and evaluated their efficacy in stimulating apoptosis in MDA‐MB 231 cells. Blank (Cs NPs) and RSV‐ Cs NPs (RSV‐Cs NPs) were synthesised via ionic gelation and characterised by using fourier‐transform infra...

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Autores principales: Bozorgi, Azam, Haghighi, Zahra, Khazaei, Mohammad Rasool, Bozorgi, Maryam, Khazaei, Mozafar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116016/
https://www.ncbi.nlm.nih.gov/pubmed/36420812
http://dx.doi.org/10.1049/nbt2.12108
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author Bozorgi, Azam
Haghighi, Zahra
Khazaei, Mohammad Rasool
Bozorgi, Maryam
Khazaei, Mozafar
author_facet Bozorgi, Azam
Haghighi, Zahra
Khazaei, Mohammad Rasool
Bozorgi, Maryam
Khazaei, Mozafar
author_sort Bozorgi, Azam
collection PubMed
description Herein, the authors synthesised chitosan nanoparticles (Cs NPs) as a resveratrol (RSV) carrier and evaluated their efficacy in stimulating apoptosis in MDA‐MB 231 cells. Blank (Cs NPs) and RSV‐ Cs NPs (RSV‐Cs NPs) were synthesised via ionic gelation and characterised by using fourier‐transform infrared spectroscopy (FTIR), Scanning electron microscope, dynamic light scattering/Zeta potential and RSV release. MDA‐MB 231 cells were treated with RSV, Cs NPs and RSV‐Cs NPs (24, 48, and 72 h), followed by the 3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide assay. Cell toxicity was evaluated using lactate dehydrogenase assay, and real‐time polymerase chain reaction was performed to explore apoptosis induction. FTIR spectra confirmed the NPs via the formation of cross‐linking bonds. Cs and RSV‐Cs NPs sizes were about 75 and 198 nm with 14 and 24 mV zeta potentials. The RSV entrapment efficiency was 52.34 ± 0.16%, with an early rapid release followed by a sustained manner. Cs and RSV‐Cs NPs inhibited cell proliferation at lower concentrations and IC50 values. RSV‐Cs NPs had the most cytotoxic effect and stimulated intrinsic apoptotic pathway, indicated by increased Bcl‐2‐associated x (BAX), BAX/Bcl‐2 ratio, P53 expressions, reduced Bcl‐2 and upregulated caspases 3, 8 and 9. RSV‐Cs NPs have a great potential to suppress invasive breast cancer cell proliferation by targeting mitochondrial metabolism and inducing the intrinsic apoptotic pathway.
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spelling pubmed-101160162023-04-21 The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment Bozorgi, Azam Haghighi, Zahra Khazaei, Mohammad Rasool Bozorgi, Maryam Khazaei, Mozafar IET Nanobiotechnol Original Research Herein, the authors synthesised chitosan nanoparticles (Cs NPs) as a resveratrol (RSV) carrier and evaluated their efficacy in stimulating apoptosis in MDA‐MB 231 cells. Blank (Cs NPs) and RSV‐ Cs NPs (RSV‐Cs NPs) were synthesised via ionic gelation and characterised by using fourier‐transform infrared spectroscopy (FTIR), Scanning electron microscope, dynamic light scattering/Zeta potential and RSV release. MDA‐MB 231 cells were treated with RSV, Cs NPs and RSV‐Cs NPs (24, 48, and 72 h), followed by the 3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide assay. Cell toxicity was evaluated using lactate dehydrogenase assay, and real‐time polymerase chain reaction was performed to explore apoptosis induction. FTIR spectra confirmed the NPs via the formation of cross‐linking bonds. Cs and RSV‐Cs NPs sizes were about 75 and 198 nm with 14 and 24 mV zeta potentials. The RSV entrapment efficiency was 52.34 ± 0.16%, with an early rapid release followed by a sustained manner. Cs and RSV‐Cs NPs inhibited cell proliferation at lower concentrations and IC50 values. RSV‐Cs NPs had the most cytotoxic effect and stimulated intrinsic apoptotic pathway, indicated by increased Bcl‐2‐associated x (BAX), BAX/Bcl‐2 ratio, P53 expressions, reduced Bcl‐2 and upregulated caspases 3, 8 and 9. RSV‐Cs NPs have a great potential to suppress invasive breast cancer cell proliferation by targeting mitochondrial metabolism and inducing the intrinsic apoptotic pathway. John Wiley and Sons Inc. 2022-11-24 /pmc/articles/PMC10116016/ /pubmed/36420812 http://dx.doi.org/10.1049/nbt2.12108 Text en © 2022 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Bozorgi, Azam
Haghighi, Zahra
Khazaei, Mohammad Rasool
Bozorgi, Maryam
Khazaei, Mozafar
The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title_full The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title_fullStr The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title_full_unstemmed The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title_short The anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
title_sort anti‐cancer effect of chitosan/resveratrol polymeric nanocomplex against triple‐negative breast cancer; an in vitro assessment
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116016/
https://www.ncbi.nlm.nih.gov/pubmed/36420812
http://dx.doi.org/10.1049/nbt2.12108
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