Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/15909
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dc.contributor.authorMooranian A.en_US
dc.contributor.authorZamani N.en_US
dc.contributor.authorTakechi R.en_US
dc.contributor.authorAl-Sallami H.en_US
dc.contributor.authorMomir Mikoven_US
dc.contributor.authorSvetlana Goločorbin-Konen_US
dc.contributor.authorBožica Kovačevićen_US
dc.contributor.authorArfuso F.en_US
dc.contributor.authorAl-Salami H.en_US
dc.date.accessioned2020-03-03T15:01:51Z-
dc.date.available2020-03-03T15:01:51Z-
dc.date.issued2019-01-01-
dc.identifier.issn20415990en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/15909-
dc.description.abstract© 2019 Newlands Press. Aim: Common features in insulin-resistance diabetes include inflammation and liver damage due to bile acid accumulation. Results & methodology: This study aimed to test in vivo pharmacological effects of combining two drugs, ursodeoxycholic acid that has bile acid regulatory effects, and probucol (PB) that has potent anti-oxidative stress effects, using a new poly(meth)acrylate nano-targeting formulation on prediabetic mice. Mice were made diabetic and were fed daily with either PB, nanoencapsulated PB or nanoencapsulated PB-ursodeoxycholic acid before blood, tissues, urine and feces were collected for inflammation and bile acid measurements. The nanoencapsulated PB-ursodeoxycholic acid formulation increased plasma IL-10, and increased the concentration of primary bile acids in the liver and heart. Conclusion: Results suggest potential applications in regulating IL-10 in insulin-resistance prediabetes.en_US
dc.language.isoenen_US
dc.relation.ispartofTherapeutic Deliveryen_US
dc.subjectinsulin resistanceen_US
dc.subjectdiabetesen_US
dc.subjectnanoencapsulationen_US
dc.subjectprobucolen_US
dc.subjectbile acidsen_US
dc.titleProbucol-poly(meth)acrylate-bile acid nanoparticles increase IL-10, and primary bile acids in prediabetic miceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.4155/tde-2019-0052-
dc.identifier.pmid10-
dc.identifier.scopus2-s2.0-85074527921-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85074527921-
dc.description.versionPublisheden_US
dc.relation.lastpage571en_US
dc.relation.firstpage563en_US
dc.relation.issue9en_US
dc.relation.volume10en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.orcidhttps://orcid.org/0000-0002-9257-8074 -
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