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Unveiling the consequences of early human saliva contamination on membranes for guided bone regeneration

dc.contributor.authorKunrath, Marcel F.
dc.contributor.authorGiraldo‐Osorno, Paula Milena
dc.contributor.authorMendes, Karina
dc.contributor.authorGomes, Ana T. P. C.
dc.contributor.authorRosa, Nuno
dc.contributor.authorBarros, Marlene
dc.contributor.authorDahlin, Christer
dc.date.accessioned2024-04-30T08:31:49Z
dc.date.available2024-04-30T08:31:49Z
dc.date.issued2024-12-01
dc.description.abstractAims: GBR membranes have various surface properties designed to elicit positive responses in regenerative clinical procedures; dental clinicians attempt to employ techniques to prevent the direct interaction of contaminated oral fluids with these biomaterials. However, saliva is uninterruptedly exhibited in oral surgical proce-dures applying GBR membranes, suggesting a persistent interaction with biomate-rials and the surrounding oral tissues. This fundamental study aimed to investigate potential alterations in the physical, chemical, and key biological properties of membranes for guided bone regeneration (GBR) caused by isolated early interac-tion with human saliva.Methods: A reproducible step- by- step protocol for collecting and interacting human saliva with membranes was developed. Subsequently, membranes were evaluated for their physicochemical properties, protein quantification, DNA, and 16S rRNA levels viability of two different cell lines at 1 and 7 days, and ALP activity. Non-interacted membranes and pure saliva of donors were applied as controls.Results: Qualitative morphological alterations were noticed; DNA extraction and 16S quantification revealed significantly higher values. Furthermore, the viability of HGF- 1 and MC3T3-E1 cells was significantly (p< .05) reduced following saliva inter-action with biodegradable membranes. Saliva contamination did not prejudice PTFE membranes significantly in any biological assay.Conclusions: These outcomes demonstrated a susceptible response of biodegrad-able membranes to isolated early human saliva interaction, suggesting impairment of structural morphology, reduced viability to HGF-1 and MC3T3-E1, and higher ab-sorption/adherence of DNA/16S rRNA. As a result, clinical oral procedures may need corresponding refinements.pt_PT
dc.description.versioninfo:eu-repo/semantics/acceptedVersionpt_PT
dc.identifier.doi10.1111/jre.13266pt_PT
dc.identifier.eid85191164351
dc.identifier.issn0022-3484
dc.identifier.pmid38644743
dc.identifier.urihttp://hdl.handle.net/10400.14/44848
dc.identifier.wos001206470600001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectBiocompatibilitypt_PT
dc.subjectDental materialspt_PT
dc.subjectGuided regenerationpt_PT
dc.subjectOral regenerationpt_PT
dc.subjectPeriodontologypt_PT
dc.subjectSalivapt_PT
dc.titleUnveiling the consequences of early human saliva contamination on membranes for guided bone regenerationpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1209
oaire.citation.issue6
oaire.citation.startPage1196
oaire.citation.titleJournal of Periodontal Researchpt_PT
oaire.citation.volume59
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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