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Polydopamine nanoparticles kill cancer cells

Polydopamine (PD) is a synthetic melanin analogue of growing importance in the field of biomedicine, especially with respect to cancer research, due, in part, to its biocompatibility. But little is known about the cytotoxic effects of PD on cancer cell lines. PD is a UV-vis absorbing material whose...

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Autores principales: Nieto, Celia, Vega, Milena A., Marcelo, Gema, Martín del Valle, Eva M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088449/
https://www.ncbi.nlm.nih.gov/pubmed/35558470
http://dx.doi.org/10.1039/c8ra05586f
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author Nieto, Celia
Vega, Milena A.
Marcelo, Gema
Martín del Valle, Eva M.
author_facet Nieto, Celia
Vega, Milena A.
Marcelo, Gema
Martín del Valle, Eva M.
author_sort Nieto, Celia
collection PubMed
description Polydopamine (PD) is a synthetic melanin analogue of growing importance in the field of biomedicine, especially with respect to cancer research, due, in part, to its biocompatibility. But little is known about the cytotoxic effects of PD on cancer cell lines. PD is a UV-vis absorbing material whose absorbance overlaps with that of formazan salts, which are used to assess cell viability in MTT assays. In this study, a protocol has been established to eliminate the contributing absorbance of PD at 550 nm, and has been applied to characterize the cytotoxicity of PD nanoparticles in both healthy and breast cancer cell lines. Once the protocol is applied, it was found that PD is per se an antineoplastic system, meaning it selectively kills cancer cells, especially those of breast cancer, but it has no toxic effect on healthy cells. The mechanism of action could be related to the production of ROS and the alteration of iron homeostasis in lysosomes. To the best of our knowledge there are only a few examples of nanoparticle systems devoid of drugs that selectively kill cancer cells.
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spelling pubmed-90884492022-05-11 Polydopamine nanoparticles kill cancer cells Nieto, Celia Vega, Milena A. Marcelo, Gema Martín del Valle, Eva M. RSC Adv Chemistry Polydopamine (PD) is a synthetic melanin analogue of growing importance in the field of biomedicine, especially with respect to cancer research, due, in part, to its biocompatibility. But little is known about the cytotoxic effects of PD on cancer cell lines. PD is a UV-vis absorbing material whose absorbance overlaps with that of formazan salts, which are used to assess cell viability in MTT assays. In this study, a protocol has been established to eliminate the contributing absorbance of PD at 550 nm, and has been applied to characterize the cytotoxicity of PD nanoparticles in both healthy and breast cancer cell lines. Once the protocol is applied, it was found that PD is per se an antineoplastic system, meaning it selectively kills cancer cells, especially those of breast cancer, but it has no toxic effect on healthy cells. The mechanism of action could be related to the production of ROS and the alteration of iron homeostasis in lysosomes. To the best of our knowledge there are only a few examples of nanoparticle systems devoid of drugs that selectively kill cancer cells. The Royal Society of Chemistry 2018-10-24 /pmc/articles/PMC9088449/ /pubmed/35558470 http://dx.doi.org/10.1039/c8ra05586f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Nieto, Celia
Vega, Milena A.
Marcelo, Gema
Martín del Valle, Eva M.
Polydopamine nanoparticles kill cancer cells
title Polydopamine nanoparticles kill cancer cells
title_full Polydopamine nanoparticles kill cancer cells
title_fullStr Polydopamine nanoparticles kill cancer cells
title_full_unstemmed Polydopamine nanoparticles kill cancer cells
title_short Polydopamine nanoparticles kill cancer cells
title_sort polydopamine nanoparticles kill cancer cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088449/
https://www.ncbi.nlm.nih.gov/pubmed/35558470
http://dx.doi.org/10.1039/c8ra05586f
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