2020
DOI: 10.1063/5.0000159
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Effect of hesperidin conjugated with golden nanoparticles on phagocytic activity: In vitro study

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Cited by 20 publications
(4 citation statements)
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“…Overall, AgNPs augmented BMDMs and phagocytosis activity due to IL-8 production. The increase in phagocytic activity is likely a consequence of the AgNPs containing chemical substances, which acted as immune stimulators and enhancers, leading to increases in the activity of BMDMs to engulf foreign bodies, such as bacterial strains [49]. A study by Fraser et al [50] verified effect of silver NP on circulating mature, CD16 bright /CD62L bright and immature, CD16 dim /CD62L bright neutrophils.…”
Section: Silver Nanoparticles Induce Phagocytic Cell Activitymentioning
confidence: 99%
“…Overall, AgNPs augmented BMDMs and phagocytosis activity due to IL-8 production. The increase in phagocytic activity is likely a consequence of the AgNPs containing chemical substances, which acted as immune stimulators and enhancers, leading to increases in the activity of BMDMs to engulf foreign bodies, such as bacterial strains [49]. A study by Fraser et al [50] verified effect of silver NP on circulating mature, CD16 bright /CD62L bright and immature, CD16 dim /CD62L bright neutrophils.…”
Section: Silver Nanoparticles Induce Phagocytic Cell Activitymentioning
confidence: 99%
“…Recently, a golden nanoparticle-conjugated hesperidin complex was produced and evaluated with respect to the stimulation of the activity of phagocytic cells [55]. The phagocytic index of the conjugated complex against Staphylococcus aureus bacteria was considerably higher (85%) in comparison with both gold nanoparticles (66%), hesperidin (51%) and untreated blood sample used as the control (20%), demonstrating its higher bioavailability.…”
Section: The Bioavailability Issuementioning
confidence: 99%
“…Briefly, Cells line was seeded with density(1×104)on the cover slide that was located at the12well plate with GNPs and Si-GNPs were added in triplicate at different concentrations, and then incubated for 72 h (IC50 concentration), were used to treat the cells in 96-well plates. After incubation 24 hours, washing with PBS (twice), and addition of 100 μL of AO/EtBr (5 min), fluorescence microscopy was applied for cell visualization [32].…”
Section: Test For Clonogenicitymentioning
confidence: 99%