Fishroesomes as carriers with antioxidant and anti-inflammatory bioactivities

The great diversity of marine habitats and organisms renders them a high-value source to find/develop novel drugs and formulations. Therefore, herein, sardine (Sardina pilchardus) roe was used as a lipidic source to produce liposomes. This fish product presents high nutritional value, being its lipi...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2021-08, Vol.140, p.111680, Article 111680
Hauptverfasser: Guedes, Marta, Vieira, Sara F., Reis, Rui L., Ferreira, Helena, Neves, Nuno M.
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Sprache:eng
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Zusammenfassung:The great diversity of marine habitats and organisms renders them a high-value source to find/develop novel drugs and formulations. Therefore, herein, sardine (Sardina pilchardus) roe was used as a lipidic source to produce liposomes. This fish product presents high nutritional value, being its lipidic content associated with important health benefits. Consequently, it can be advantageously used to produce therapeutically active delivery devices. Roe lipids were extracted using the Matyash method. After lipid film hydration and extrusion, sardine roe-derived large unilamellar liposomes (LUVs), designated as fishroesomes, presented a size of ≈330 nm and a significant negative surface charge (≈−27 mV). Radical scavenging assays demonstrated that fishroesomes efficiently neutralized peroxyl, hydroxyl and nitric oxide radicals. Moreover, fishroesomes significantly reduced the expression of pro-inflammatory cytokines and chemokines by LPS-stimulated macrophages at non-toxic concentrations for L929 and THP-1 cells. Consequently, the developed liposomes exhibit unique properties as bioactive drug carriers for inflammatory diseases treatment. [Display omitted] •Fishroesomes were produced from lipidic extracts of sardine roe.•Fishroesomes had antioxidant and anti-inflammatory actions at cytocompatible levels.•Bioactivity was often similar or higher than positive controls (e.g., dexamethasone).•Fishroesomes may be a valid formulation for the treatment of inflammatory diseases.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2021.111680