Anti-inflammatory, analgesic and anti-tumor properties of gold nanoparticles
Anti-inflammatory, analgesic and anti-tumor properties of gold nanoparticles
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DOI:
10.1016/j.pharep.2016.09.017
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发表时间:
2017-01-01
影响因子:
4.4
通讯作者:
Gasparotto, Luiz H. S.
中科院分区:
文献类型:
--
作者:
de Araujo Junior, Raimundo Fernandes;de Araujo, Aurigena Antunes;Gasparotto, Luiz H. S.
Background: Gold nanoparticles (GNPs) are regarded as potential platforms for drug delivery. However, their interaction with live organisms must be understood prior to their utilization as drug carriers. The present study reports the anti-inflammatory, analgesic and anti-tumor effects of GNPs. The biodistribution of GNPs and their effect on various tissues have also been studied.Methods: GNPs were synthesized through an environmentally friendly route and characterized with TEM and UV-vis. After HT-29 cells had been exposed to GNPs, apoptosis was assessed with Annexin V and propidium iodide staining and caspase-3 activity determined with a confocal laser scanning microscope. GNPs were administrated to male and female Swiss mice for posterior assessment of their antiinflammatory and analgesic properties. The biodistribution of GNPs and their impact on tissues were studied with UV-vis and histopathological analysis, respectively.Results: Cell apoptosis was observed in a dose-dependent manner for GNPs concentrations ranging from 40 mu g/mL to 80 mu g/mL (p < 0.05). The best anti-inflammatory activity was observed at the dose of 1500 mu g/kg, which caused a reduction of 49.3% in leukocyte migration. GNPs showed peripheral analgesia at the dose of 1500 mu g/kg and have been found in liver, spleen, kidney and lungs. Histopathological examination revealed extravasation of red blood cells in lungs.Conclusion: The study draws attention to gold nanoparticles as a resource for technological innovation in the anti-inflammatory, analgesic and anti-tumor fields. GNPs have biological effects that deserve investigation to assess their full interaction with organic systems. (C) 2016 Published by Elsevier Sp. z o.o. on behalf of Institute of Pharmacology, Polish Academy of Sciences.