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Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment
Inflammation, oxidative stress, and uncontrolled cell proliferation are common key features of chronic inflammatory diseases, such as atherosclerosis and cancer. ω3 polyunsaturated fatty acids (PUFAs; also known as omega3 fatty acids or fish oil) have beneficial effects against inflammation upon die...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063558/ https://www.ncbi.nlm.nih.gov/pubmed/27785012 http://dx.doi.org/10.2147/IJN.S115995 |
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author | Alaarg, Amr Jordan, Nan Yeun Verhoef, Johan JF Metselaar, Josbert M Storm, Gert Kok, Robbert J |
author_facet | Alaarg, Amr Jordan, Nan Yeun Verhoef, Johan JF Metselaar, Josbert M Storm, Gert Kok, Robbert J |
author_sort | Alaarg, Amr |
collection | PubMed |
description | Inflammation, oxidative stress, and uncontrolled cell proliferation are common key features of chronic inflammatory diseases, such as atherosclerosis and cancer. ω3 polyunsaturated fatty acids (PUFAs; also known as omega3 fatty acids or fish oil) have beneficial effects against inflammation upon dietary consumption. However, these effects cannot be fully exploited unless diets are enriched with high concentrations of fish oil supplements over long periods of time. Here, a nanomedicine-based approach is presented for delivering effective levels of PUFAs to inflammatory cells. Nanoparticles are internalized by immune cells, and hence can adequately deliver bioactive lipids into these target cells. The ω3 FA docosahexaenoic acid was formulated into liposomes (ω-liposomes), and evaluated for anti-inflammatory effects in different types of immune cells. ω-Liposomes strongly inhibited the release of reactive oxygen species and reactive nitrogen species from human neutrophils and murine macrophages, and also inhibited the production of the proinflammatory cytokines TNFα and MCP1. Moreover, ω-liposomes inhibited tumor-cell proliferation when evaluated in FaDu head and neck squamous carcinoma and 4T1 breast cancer cells in in vitro cultures. We propose that ω-liposomes are a promising nanonutraceutical formulation for intravenous delivery of fish oil FAs, which may be beneficial in the treatment of inflammatory disorders and cancer. |
format | Online Article Text |
id | pubmed-5063558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50635582016-10-26 Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment Alaarg, Amr Jordan, Nan Yeun Verhoef, Johan JF Metselaar, Josbert M Storm, Gert Kok, Robbert J Int J Nanomedicine Original Research Inflammation, oxidative stress, and uncontrolled cell proliferation are common key features of chronic inflammatory diseases, such as atherosclerosis and cancer. ω3 polyunsaturated fatty acids (PUFAs; also known as omega3 fatty acids or fish oil) have beneficial effects against inflammation upon dietary consumption. However, these effects cannot be fully exploited unless diets are enriched with high concentrations of fish oil supplements over long periods of time. Here, a nanomedicine-based approach is presented for delivering effective levels of PUFAs to inflammatory cells. Nanoparticles are internalized by immune cells, and hence can adequately deliver bioactive lipids into these target cells. The ω3 FA docosahexaenoic acid was formulated into liposomes (ω-liposomes), and evaluated for anti-inflammatory effects in different types of immune cells. ω-Liposomes strongly inhibited the release of reactive oxygen species and reactive nitrogen species from human neutrophils and murine macrophages, and also inhibited the production of the proinflammatory cytokines TNFα and MCP1. Moreover, ω-liposomes inhibited tumor-cell proliferation when evaluated in FaDu head and neck squamous carcinoma and 4T1 breast cancer cells in in vitro cultures. We propose that ω-liposomes are a promising nanonutraceutical formulation for intravenous delivery of fish oil FAs, which may be beneficial in the treatment of inflammatory disorders and cancer. Dove Medical Press 2016-10-05 /pmc/articles/PMC5063558/ /pubmed/27785012 http://dx.doi.org/10.2147/IJN.S115995 Text en © 2016 Alaarg et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Alaarg, Amr Jordan, Nan Yeun Verhoef, Johan JF Metselaar, Josbert M Storm, Gert Kok, Robbert J Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title | Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title_full | Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title_fullStr | Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title_full_unstemmed | Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title_short | Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
title_sort | docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063558/ https://www.ncbi.nlm.nih.gov/pubmed/27785012 http://dx.doi.org/10.2147/IJN.S115995 |
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