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Estudio2016Financiación no declaradaSolo mecanismosAcceso abierto

Docosahexaenoic acid liposomes for targeting chronic inflammatory diseases and cancer: an in vitro assessment

Alaarg A, Jordan NY, Verhoef JJ, Metselaar JM, Storm G, Kok RJ

International journal of nanomedicine · 37 citas

Etiquetas de revisión

Financiación no declaradaSolo mecanismos

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Cómo se estudió

Diseño
Estudio in vitro o de mecanismos (clasificado por nuestro filtro de IA)
Estudiado en
Personas, más trabajo en animales o laboratorio
Resultado principal
Solo mecanismos

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2016-10-01 · Int J Nanomedicine · vol. Volume 11 · págs. 5027–5040
Editorial
Dove Medical Press
Citado
59 citas · más que el 95% de estudios similares · 4.7× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
48 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC
Áreas de investigación
Fatty Acid Research and Health · Cholesterol and Lipid Metabolism · Eicosanoids and Hypertension Pharmacology
Palabras clave
Docosahexaenoic acid, Fish oil, Proinflammatory cytokine, Polyunsaturated fatty acid, Inflammation, Liposome, Immune system, Eicosapentaenoic acid, Cancer, Cancer cell, Cancer research, Pharmacology, Reactive oxygen species, Chemistry, Immunology, Medicine, Biology, Biochemistry, Fatty acid, Internal medicine
MeSH
monocytes, cells, cultured, macrophages, animals, humans, mice, carcinoma, squamous cell, breast neoplasms, inflammation, reactive nitrogen species, reactive oxygen species, docosahexaenoic acids, tumor necrosis factor-alpha, cytokines, liposomes, cell proliferation, oxidative stress, female, human umbilical vein endothelial cells, in vitro techniques

6 autores

  • Amr Alaarg🇳🇱Utrecht University; University of Twente
  • Nan Yeun Jordan🇳🇱Utrecht University; Pharmo Institute; University of Twente
  • Johan J. F. Verhoef🇳🇱Utrecht University; Pharmo Institute
  • Josbert M. Metselaar🇳🇱🇩🇪Utrecht University; Pharmo Institute; RWTH Aachen University; University of Twente
  • Gert Storm🇳🇱Utrecht University; Pharmo Institute; University of Twente
  • Robbert J. Kok🇳🇱Utrecht University; Pharmo Institute

Resumen

El texto original del estudio, en el idioma en que se publicó.

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.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC).

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