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dc:titleHistomorphometric Evaluation of Subchronic and Chronic Effects of Novel Experimental Calcium Aluminate- and Calcium Silicate-Based Dental Cement Materials on Rat Liver, Kidney, Brain, and Spleen Tissues
dc:creatorIlić, V.
dc:creatorSmiljanić-Milutinović, S.
dc:creatorBiočanin, Vladimir
dc:creatorKuzmanović Pfićer, J.
dc:creatorTasić, T
dc:creatorDanilović, V.
dc:creatorJapundžić-Žigon, N.
dc:creatorParaš, S.
dc:creatorJokanović, V.
dc:creatorĆetković, D.
dc:creatorAntonijević, Đ.
dc:subjectcalcium silicate cements
dc:subjectcalcium aluminate cement
dc:subjectdental cements
dc:subjectzirconia
dc:subjectmineral trioxide aggregate
dc:subjectbiocompatibility
dc:subjecthistomorphometry
dc:subjectliver
dc:subjectkidney
dc:subjectbrain
dc:subjectspleen
dc:subjectlymphoid follicles
dc:subjectrats
dc:descriptionAlthough biocompatible calcium silicate cements (CSCs) and calcium aluminate cements (CACs) may induce local and systemic adverse effects. This study aimed to evaluate the subchronic and chronic effects of experimental CAC and CSC mixtures on rat liver, kidney, brain, and spleen tissue. Two experimental mixtures, CAC with added ZrO2 (ECCA + ZrO2) and CSC with added ZrO2 (ECCS + ZrO2), and mineral trioxide aggregate (MTA), were implanted intraalveolary in 36 male Wistar rats. Histomorphometry was conducted after 30 and 180 days on liver, kidney, brain, and spleen. Consistent results were observed in all material groups. Liver tissue inflammation ranged from none to minimal for all three materials. In kidney, ECCA + ZrO2 displayed a slightly better result than other two materials. In brain, after 180 days, both ECCA + ZrO2 and MTA showed a statistically significant reduction in perineural vacuolation (p < 0.05), and MTA showed a reduction in the percentage of intravascular congestion (p < 0.05). In spleen, a larger lymphoid follicle diameter was observed for ECCS + ZrO2 chronic group compared to other two materials (p < 0.05). ECCA + ZrO2, ECCS + ZrO2, and MTA caused none to minimal changes in liver, kidney, brain, and spleen following subchronic and chronic exposure.
dc:publisherMultidisciplinary Digital Publishing Institute
dc:date2026
dc:typeinfo:eu-repo/semantics/article
dc:typeinfo:eu-repo/semantics/publishedVersion
dc:identifierhttps://stomatoloskifakultet.rs/nauka/publikacija/1017
dc:identifierDOI 10.3390/jfb17050253
dc:identifierISSN 2079-4983
dc:sourceJournal of Functional Biomaterials 17(5): 253
dc:languageen
dc:rightsinfo:eu-repo/semantics/closedAccess
dc:rightsSva prava zadržana