Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/9684
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dc.contributor.authorL. Heinrichen_US
dc.contributor.authorO. Korzhenkoen_US
dc.contributor.authorL. Bausen_US
dc.contributor.authorK. Borrmannen_US
dc.contributor.authorB. Greveen_US
dc.contributor.authorIrina A. Kurzinaen_US
dc.date.accessioned2020-02-10T08:11:48Z-
dc.date.available2020-02-10T08:11:48Z-
dc.date.issued2017-
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/9684-
dc.description.abstractThe secondarily generated reactive oxygen radical species (ROS) play a crucial role in the radiotherapy due to their cell toxicity. Topically applied antioxidants to skin or open tissues are targeted to protect healthy tissue against irradiation associated damages. While the radioprotective effects of the antioxi- dants to the keratinocyte cell line HaCaT and the breast tumor cell line MCF-7 can be demonstrated by radiation experiments, their stability against oxygen in the formulation phase is insufficient. Stabiliza- tion against oxidation by cyclodextrin (CD) inclusion complexes and liposomes seems be a promising option.en_US
dc.language.isoenen_US
dc.titleStabilization of antioxidative drugs against premature oxidationen_US
dc.typeConference Paperen_US
dc.relation.conferenceXIV International Conference „Development perspectives of the fundamental sciences“en_US
dc.description.versionPublisheden_US
item.grantfulltextopen-
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Appears in Collections:Naučne i umetničke publikacije
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