Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/22278

TitleAntiproliferative activity of fucan nanogel
Author(s)Santos, Nednaldo Dantas
Lima, Jailma Almeida
Vidal, Arthur Anthunes Jacome
Oliveira, Ruth Medeiros
Pedrosa, Sílvia Santos
Pereira, Paula
Gama, F. M.
Rocha, Hugo Alexandre Oliveira
Gomes, Dayanne Lopes
KeywordsNanogelFucan
Nanogels
Cancer cells
Sulfated polysaccharides
Spatoglossum schröederi
Spatoglossum schroederi
Issue date2012
PublisherMDPI
JournalMarine Drugs
Abstract(s)Sulfated fucans comprise families of polydisperse natural polysaccharides based on sulfated l-fucose. Our aim was to investigate whether fucan nanogel induces cell-specific responses. To that end, a non toxic fucan extracted from Spatoglossum schröederi was chemically modified by grafting hexadecylamine to the polymer hydrophilic backbone. The resulting modified material (SNFuc) formed nanosized particles. The degree of substitution with hydrophobic chains was close to 100%, as estimated by elemental analysis. SNFfuc in aqueous media had a mean diameter of 123 nm and zeta potential of −38.3 ± 0.74 mV, as measured by dynamic light scattering. Nanoparticles conserved their size for up to 70 days. SNFuc cytotoxicity was determined using the MTT assay after culturing different cell lines for 24 h. Tumor-cell (HepG2, 786, H-S5) proliferation was inhibited by 2.0%–43.7% at nanogel concentrations of 0.05–0.5 mg/mL and rabbit aorta endothelial cells (RAEC) non-tumor cell line proliferation displayed inhibition of 8.0%–22.0%. On the other hand, nanogel improved Chinese hamster ovary (CHO) and monocyte macrophage cell (RAW) non-tumor cell line proliferation in the same concentration range. The antiproliferative effect against tumor cells was also confirmed using the BrdU test. Flow cytometric analysis revealed that the fucan nanogel inhibited 786 cell proliferation through caspase and caspase-independent mechanisms. In addition, SNFuc blocks 786 cell passages in the S and G2-M phases of the cell cycle.
TypeArticle
URIhttp://hdl.handle.net/1822/22278
DOI10.3390/md10092002
ISSN1660-3397
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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