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dc.contributor.authorKara, Özlem
dc.contributor.authorŞeşeoğulları Dirihan, Roda
dc.contributor.authorSayın Özel, Gülsüm
dc.contributor.authorTezvergil Mutluay, Arzu
dc.contributor.authorÜşümez, Aslıhan
dc.date.accessioned2021-10-13T12:49:52Z
dc.date.available2021-10-13T12:49:52Z
dc.date.issued2021en_US
dc.identifier.citationKara, Ö., Şeşeoğulları Dirihan, R., Sayın Özel, G., Tezvergil Mutluay, A. ve Üşümez, A. (2021). Inhibition of cathepsin-K and matrix metalloproteinase by photodynamic therapy. Dental Materials, 37(10), e485-e492. https://dx.doi.org/10.1016/j.dental.2021.08.015en_US
dc.identifier.issn0109-5641
dc.identifier.issn1879-0097
dc.identifier.urihttps://dx.doi.org/10.1016/j.dental.2021.08.015
dc.identifier.urihttps://hdl.handle.net/20.500.12511/8443
dc.description.abstractObjectives: The objective of this study was to determine the effects of antimicrobial photodynamic therapy (aPDT) with indocyanine green (ICG) and toluidine blue (TB) on protease activity (matrix-bound cathepsin K and matrix metalloproteinase (MMP) and dentin bond strength. Methods: Caries-free human third molars were assigned to five groups: 1—control group, 2—application of ICG with activation using an 810 nm diode (aPDT), 3—application of ICG, 4—application of TB with activation using a 660 nm diode (aPDT), and 5—application of TB. For the enzymatic investigation, dentin beams were incubated for either 3 days or 3 weeks. Aliquots of the incubation media were analyzed by ELISA for CTX (C-terminal cross-linked telopeptide of type I Collagen) and ICTP (cross-linked carboxy-terminal telopeptide of type I collagen). For microtensile bond strength testing (μTBS), composite resins were layered onto the tooth surface; the samples were then subjected to μTBS. Kruskall–Wallis and Mann–Whitney U tests were applied for statistical analysis of CTX and ICTP, one way-ANOVA and Tukey's test were applied for statistical analysis of μTBS. Results: Pretreating the dentin matrices with aPDT decreased the endogenous protease activity. ICG with laser activation resulted in the highest μTBS. Therefore, aPDT should be considered as a treatment method because it can reduce MMP-mediated dentin degradation and increase the μTBS. Significance: Inhibiting endogenous protease activity improves the stability of the dentin–adhesive bond and the durability of the bond strength.en_US
dc.language.isoengen_US
dc.publisherElsevier Inc.en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectAntimicrobial Photodynamic Therapyen_US
dc.subjectCTXen_US
dc.subjectICTPen_US
dc.subjectIndocyanine Greenen_US
dc.subjectMicrotensile Bond Strengthen_US
dc.subjectToluidine Blueen_US
dc.titleInhibition of cathepsin-K and matrix metalloproteinase by photodynamic therapyen_US
dc.typearticleen_US
dc.relation.ispartofDental Materialsen_US
dc.departmentİstanbul Medipol Üniversitesi, Diş Hekimliği Fakültesi, Protetik Diş Tedavisi Ana Bilim Dalıen_US
dc.authorid0000-0001-8833-5259en_US
dc.identifier.volume37en_US
dc.identifier.issue10en_US
dc.identifier.startpagee485en_US
dc.identifier.endpagee492en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.dental.2021.08.015en_US
dc.identifier.wosqualityQ1en_US
dc.identifier.scopusqualityQ1en_US


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