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dc.creatorMilenković, Ivana
dc.creatorRadotić, Ksenija
dc.creatorMatović, Branko
dc.date.accessioned2023-03-22T08:32:16Z
dc.date.available2023-03-22T08:32:16Z
dc.date.issued2015
dc.identifier.isbn978-3-7369-9098-2
dc.identifier.urihttp://rimsi.imsi.bg.ac.rs/handle/123456789/1841
dc.description.abstractCeO2 (nanoceria) is the most important rare-earth oxide, which application is rapidly emerging. These nanoparticles are potent free radical scavengers, due to coexistence of Ce3+ and Ce4+ ions and formation of oxygen vacancies on their surface. These ions are promising candidates for improving the treatment of cancers, drug delivery and catalysis. First, they collect reactive oxygen species (ROS) and protect healthy cells from oxidative stress. Also, they show cytotoxicity, which can be manipulated for treatment of cancer cells by inducing targeted cell death with minimal toxicity to surrounding healthy cells. This dual behavior of nanoceria presents a great pharmacological potential. We established the method for synthesizing these nanoparticles. This was particularly challenging because of their low solubility. We further coated these nanoparticles with glucose to facilitate entry into the cells. Untill now, anticancer properties of nanoceria have been poorly characterized. Hence, the aim of this work was to investigate the cytotoxic effect of nanoceria in several cancer cell lines. Nanoceria can be beneficial for the improvement of cancer treatments and a promising candidate for further medical aplication.sr
dc.language.isoensr
dc.publisherInternational Max Planck Research School for Molecular Biology in Gottingensr
dc.relationProject ID Project Title info:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45012/RS//sr
dc.rightsopenAccesssr
dc.source12th International PhD Student Symposium Horizons in Molecular Biologysr
dc.subjectAnticancer propertiessr
dc.subjectCeO2sr
dc.subjectTreatmentsr
dc.titleAnticancer properties of nanoceriasr
dc.typeconferenceObjectsr
dc.rights.licenseARRsr
dc.citation.spage101
dc.identifier.fulltexthttp://rimsi.imsi.bg.ac.rs/bitstream/id/4709/bitstream_4709.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_rimsi_1841
dc.type.versionpublishedVersionsr


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