Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/827
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dc.contributor.authorBabić, Marija M.en_US
dc.contributor.authorBožić, Bojanen_US
dc.contributor.authorBožić, Biljanaen_US
dc.contributor.authorFilipović, Jovanka M.en_US
dc.contributor.authorUšćumlić, Gordana S.en_US
dc.contributor.authorTomić, Simonida Ljen_US
dc.date.accessioned2019-07-12T21:13:11Z-
dc.date.available2019-07-12T21:13:11Z-
dc.date.issued2015-09-25-
dc.identifier.issn0022-2461-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/827-
dc.description.abstractA series of dual-sensitive poly(2-hydroxyethyl acrylate/itaconic acid) (P(HEA/IA)) hydrogels were synthesized and evaluated as drug delivery systems for potential antiproliferative agents. Investigated hydrophobic compounds, Mn(II) and Zn(II) complexes with Oxaprozin, were efficiently loaded into the P(HEA/IA) hydrogels, which was confirmed by FTIR and UV–Vis spectroscopy. Swelling studies, conducted in the physiological pH range of 2.20–8.00 and in temperature range of 30–50 °C, demonstrated that loaded transition metal complexes in P(HEA/IA) hydrogels did not annul pH and temperature sensitivity of the hydrogels. In vitro antiproliferative activity of Mn(II) and Zn(II) complexes with Oxaprozin against human cervical (HeLa) and melanoma cancer (Fem X) cell lines was tested. Results of in vitro release study investigated at different pH conditions confirmed P(HEA/IA) hydrogels as a highly effective pH-triggered drug delivery system for hydrophobic antiproliferative agents. These performances indicate that P(HEA/IA) hydrogels loaded with transition metal complexes can be further studied as a promising candidate for anticancer therapy, as well as for targeted treatment of intestine/colon cancers.en_US
dc.relation.ispartofJournal of Materials Scienceen_US
dc.titleEvaluation of poly(hydroxyethyl acrylate/itaconic acid) hydrogels for controlled delivery of transition metal complexes with Oxaprozin as potential antiproliferative agentsen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s10853-015-9179-6-
dc.identifier.scopus2-s2.0-84934952070-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84934952070-
dc.description.rankM21en_US
dc.description.impact2.599en_US
dc.description.startpage6208en_US
dc.description.endpage6219en_US
dc.description.volume50en_US
dc.description.issue18en_US
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0001-9910-2741-
crisitem.author.orcid0000-0002-1238-1731-
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