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dc.creatorParaš, Smiljana
dc.creatorJanković, Ognjenka
dc.creatorTrišić, Dijana
dc.creatorČolović, Božana M.
dc.creatorMitrović‐Ajtić, Olivera
dc.creatorDekić, Radoslav
dc.creatorSoldatović, Ivan A.
dc.creatorŽivković-Sandić, Marija
dc.creatorŽivković, Slavoljub
dc.creatorJokanović, Vukoman R.
dc.date.accessioned2020-04-30T16:30:23Z
dc.date.available2020-04-30T16:30:23Z
dc.date.issued2019
dc.identifier.issn0143-2885
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/8557
dc.description.abstractAim: To examine the potential systemic toxicity of nanostructured materials based on calcium silicate and calcium aluminate, for potential application in Dentistry. Methodology: Twenty-four Albino Wistar rats aged 2 months were used as an in vivo animal model for subcutaneous implantation of the investigated materials, placed in polyethylene tubes. Thirty days after implantation, the livers of the rats were analysed and following histological and stereological parameters were evaluated for volume density of hepatocytes and blood sinusoids, number and numerical density of hepatocytes, surface of hepatocytes and their nucleuses, nucleocytoplasmic ratio and mitotic index of hepatocytes. Stereological measurements were achieved using Cavalieri's principle, with grid P2 and unbiased analysis. Additionally, immunohistochemistry studies were performed to further analyse changes in liver tissue. Several haematological and biochemical parameters of blood of experimental animals were also analysed, as well as local tissue reactions around the implants. Statistical analysis was performed using parametric (anova and t-test) and nonparametric tests (Kruskal–Wallis and Mann–Whitney U-test) depending on data distribution. Results: Implanted dental cements led to an increase in stereological and histological parameters in liver tissue compared to control rats. Although the investigated parameters mostly showed significant differences between control and experimental animals, the liver tissue of the experimental animals did not have visible signs of pathological changes. This was supported by the analysis of blood parameters which were not significantly different between control and experimental animals. Also, the subcutaneous tissues had minimal inflammatory reactions. Immunohistochemistry studies revealed that nanostructured materials induced proliferation of hepatocytes, but that the immunological response to the materials was not strong enough to induce proliferation of immunoreactive cells in liver in the observed time period. Conclusions: This study was performed as a contribution to the attestation of the biocompatibility of dental cements based on calcium silicate and calcium aluminate. Although these materials induced several changes in the liver structure, they were not clinically relevant and represent a normal and reversible response of the liver to the presence of biocompatible materials in the body. Blood and immunohistochemistry analyses and local tissue reactions further confirmed that these materials possess good biocompatible potential. © 2019 International Endodontic Journal. Published by John Wiley & Sons Ltden
dc.language.isoen
dc.relationMinistry of Science and Technology of the Republic of Srpska
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172026/RS//
dc.rightsrestrictedAccess
dc.sourceInternational Endodontic Journal
dc.subjectbiocompatibilityen
dc.subjectcalcium aluminateen
dc.subjectcalcium silicateen
dc.subjectliveren
dc.subjectnanostructured materialen
dc.subjectstereologyen
dc.titleInfluence of nanostructured calcium aluminate and calcium silicate on the liver: histological and unbiased stereological analysisen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractЧоловић, Б; Митровић‐Aјтић, О.; Декић, Р; Солдатовић, И; Живковић Сандић, М; Живковић, С; Јокановић, В; Тришић, Д; Параш, С; Јанковић, О;
dc.rights.holder© 2019 International Endodontic Journal. Published by John Wiley & Sons Ltd
dc.citation.spage1162
dc.citation.epage1172
dc.identifier.wos000475393800008
dc.identifier.doi10.1111/iej.13105
dc.citation.rankaM21
dc.identifier.pmid30802977
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85063529347


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