dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversity of Minho
dc.contributorICVS/3B's-PT Government Associate Laboratory
dc.date.accessioned2021-06-25T10:49:46Z
dc.date.accessioned2022-12-19T22:25:41Z
dc.date.available2021-06-25T10:49:46Z
dc.date.available2022-12-19T22:25:41Z
dc.date.created2021-06-25T10:49:46Z
dc.date.issued2021-01-01
dc.identifierNanomedicine, v. 16, n. 1, p. 5-17, 2021.
dc.identifier1748-6963
dc.identifier1743-5889
dc.identifierhttp://hdl.handle.net/11449/207152
dc.identifier10.2217/nnm-2020-0312
dc.identifier2-s2.0-85099547905
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5387749
dc.description.abstractAim: To established a simple, controlled and reproducible method to synthesize gallium (Ga)-coated polydopamine (PDA) nanoparticles (NPs). Materials & methods: PDA NPs were synthesized in alkali medium with posterior Ga shell formation due to ion chelation on the NP surface. Results: The obtained results with energy-dispersive X-ray spectroscopy confirmed the incorporation of Ga on the PDA NP surface. The cytotoxicity of Ga-coated PDA NPs was evaluated in vitro at different concentrations in contact with human adipose-derived stem cells. Further cell analysis also demonstrated the benefit of Ga-coated PDA NPs, which increased the cell proliferation rate compared with noncoated PDA NPs. Conclusion: This study indicated that Ga could work as an appropriate shell for PDA NPs, inducing cell proliferation at the analyzed concentrations.
dc.languageeng
dc.relationNanomedicine
dc.sourceScopus
dc.subjectcore/shell
dc.subjectcytotoxicity
dc.subjectgallium incorporation
dc.subjectnanoparticle synthesis
dc.titleSynthesis of mussel-inspired polydopamine-gallium nanoparticles for biomedical applications
dc.typeArtículos de revistas


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