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dc.contributor.authorVural, G.
dc.contributor.authorYardımcı, Mehmet
dc.contributor.authorKoçak, Melek
dc.contributor.authorYaşar, Tuba Özge
dc.contributor.authorKurt, A.
dc.contributor.authorHarem, İsmail Şah
dc.contributor.authorCasulli, Adriano
dc.date.accessioned2022-05-11T14:42:29Z
dc.date.available2022-05-11T14:42:29Z
dc.date.issued2020
dc.identifier.issn0031-1820
dc.identifier.issn1469-8161
dc.identifier.urihttps://doi.org/10.1017/S0031182020001225
dc.identifier.urihttps://hdl.handle.net/20.500.11776/9390
dc.description.abstractIn this study, we evaluated the efficacy, expressed as a mean weight decrease of the whole echinococcal cyst mass, of novel benzimidazole salt formulations in a murine Echinococcus granulosus infection model. BALB/c mice were intraperitoneally infected with protoscoleces of E. granulosus (genotype G1). At 9 months post-infection, treatment with albendazole (ABZ), ricobendazole (RBZ) salt formulations, and RBZ enantiomer salts (R)-(+)-RBZ-Na and (S)-(-)-RBZ-Na formulations were initiated. Drugs were orally applied by gavage at 10 mg kg(-1) body weight per day during 30 days. Experimental treatments with benzimidazole sodium salts resulted in a significant reduction of the weight of cysts compared to conventional ABZ treatment, except for the (S)-(-)-RBZ-Na enantiomer formulation. Scanning electron microscopy and histological inspection revealed that treatments impacted not only the structural integrity of the parasite tissue in the germinal layer, but also induced alterations in the laminated layer. Overall, these results demonstrate the improved efficacy of benzimidazole salt formulations compared to conventional ABZ treatment in experimental murine cystic echinococcosis.en_US
dc.description.sponsorshipEuropean UnionEuropean Commission [602051]en_US
dc.description.sponsorshipThe research leading to these results received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under the project HERACLES (http://www.heracles-fp7.eu/), grant agreement no. 602051. The funder of the study had no role in study design, data collection, data analysis, data interpretation or writing of the report.en_US
dc.language.isoengen_US
dc.publisherCambridge Univ Pressen_US
dc.identifier.doi10.1017/S0031182020001225
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAlbendazoleen_US
dc.subjectEchinococcus granulosusen_US
dc.subjectefficacyen_US
dc.subjectenantiomersen_US
dc.subjectmouse modelen_US
dc.subjectnew formulationsen_US
dc.subjectricobendazoleen_US
dc.subjectsalts of benzimidazolesen_US
dc.subjectsalts of ricobendazoleen_US
dc.subjectsecondary cystic echinococcosisen_US
dc.subjectSulfoxide Enantiomersen_US
dc.subjectIn-Vitroen_US
dc.subjectGranulosusen_US
dc.subjectFlubendazoleen_US
dc.subjectNitazoxanideen_US
dc.subjectBurdenen_US
dc.titleEfficacy of novel albendazole salt formulations against secondary cystic echinococcosis in experimentally infected miceen_US
dc.typearticleen_US
dc.relation.ispartofParasitologyen_US
dc.departmentFakülteler, Veteriner Fakültesi, Temel Bilimler Bölümü, Histoloji ve Embriyoloji Ana Bilim Dalıen_US
dc.authorid0000-0001-9183-7591
dc.authorid0000-0001-9183-7591
dc.authorid0000-0002-8698-9440
dc.authorid0000-0003-2672-5766
dc.authorid0000-0002-0622-2128
dc.authorid0000-0002-5947-4118
dc.identifier.volume147en_US
dc.identifier.issue13en_US
dc.identifier.startpage1425en_US
dc.identifier.endpage1432en_US
dc.institutionauthorKoçak, Melek
dc.institutionauthorYardımcı, Mehmet
dc.institutionauthorYaşar, T. O.
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid23971786000
dc.authorscopusid57218705593
dc.authorscopusid57190291855
dc.authorscopusid57218705880
dc.authorscopusid12545052400
dc.authorscopusid57212700878
dc.authorscopusid12781515600
dc.authorwosidHAREM, Ismail Sah/ABG-8821-2020
dc.authorwosidCasulli, Adriano/AAQ-6859-2020
dc.authorwosidCarradori, Simone/S-4776-2019
dc.authorwosidCASULLI, ADRIANO/O-2278-2015
dc.authorwosidLundstrom-Stadelmann, Britta/E-8042-2011
dc.identifier.wosWOS:000590482000006en_US
dc.identifier.scopus2-s2.0-85090156361en_US
dc.identifier.pmid32729453en_US


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