Long-Term Inflammatory Response to Liquid Injectable Silicone, Cartilage, and Silicone Sheet

dc.contributor.authorHizal, Evren
dc.contributor.authorBuyuklu, Fuat
dc.contributor.authorOzdemir, B. Handan
dc.contributor.authorErbek, Selim S.
dc.contributor.orcIDhttps://orcid.org/0000-0002-9699-6783en_US
dc.contributor.orcIDhttps://orcid.org/0000-0003-1528-0036en_US
dc.contributor.orcIDhttps://orcid.org/0000-0002-7528-3557en_US
dc.contributor.orcIDhttps://orcid.org/0000-0003-4825-3499en_US
dc.contributor.pubmedID24966072en_US
dc.contributor.researcherIDA-5853-2018en_US
dc.contributor.researcherIDW-5941-2018en_US
dc.contributor.researcherIDX-8540-2019en_US
dc.contributor.researcherIDB-7604-2019en_US
dc.date.accessioned2023-12-20T12:37:26Z
dc.date.available2023-12-20T12:37:26Z
dc.date.issued2014
dc.description.abstractObjectives/HypothesisTo show and compare the long-term inflammatory responses to subdermal microdroplet injections of 1,000 centistoke (cS) and 5,000 cS liquid injectable silicone (LIS), and to assess the applicability of insulin pen as an alternative LIS delivery device in an animal model. Study DesignAnimal study. MethodsEighteen healthy adult Sprague-Dawley rats were used. Two graft recipient sites and four injection sites were prepared on each rat's back for: 1) autogenous auricular cartilage graft; 2) silicone sheet; 3) 1,000 cS LIS injection with insulin syringe; 4) 1,000 cS LIS injection with insulin pen; 5) 5,000 cS LIS injection with insulin syringe; and 6) 5,000 cS LIS injection with insulin pen. The animals were followed up for 6 months, and skin biopsies were examined for the evaluation of LIS microdroplets in situ and the degree of inflammatory tissue response. Immunohistochemistry was used for the examination of macrophages and the density of microvessels. ResultsBiopsies from 17 animals were assessed. There was no statistically significant difference among the groups in terms of the number of lymphocytes (P=0.081), macrophages (P=0.857), and neutrophils (P=0.995), the degree of vascular proliferation (P=0.698), and the mean LIS microdroplet diameter (P=0.540). Grossly, there was no sign of granuloma formation in any of the specimens. ConclusionThere is a low-grade, well-tolerated long-term inflammatory response to microdroplet injections of 1,000 cS and 5,000 cS LIS that is comparable to autogenous cartilage graft in rats. Standard dose delivery devices such as insulin pens can be used for controlled LIS injections. Level of EvidenceN/A. Laryngoscope, 124:E425-E430, 2014en_US
dc.identifier.endpage430en_US
dc.identifier.issn0023-852Xen_US
dc.identifier.issue11en_US
dc.identifier.scopus2-s2.0-84922332342en_US
dc.identifier.startpage425en_US
dc.identifier.urihttp://hdl.handle.net/11727/11150
dc.identifier.volume124en_US
dc.identifier.wos000344382100001en_US
dc.language.isoengen_US
dc.relation.isversionof10.1002/lary.24800en_US
dc.relation.journalLARYNGOSCOPEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSiliconeen_US
dc.subjectliquid injectable siliconeen_US
dc.subject1000 centistokeen_US
dc.subject5000 centistokeen_US
dc.subjectdermal filleren_US
dc.subjectinjectable filleren_US
dc.subjectinflammationen_US
dc.subjectautogenous cartilageen_US
dc.subjectrhinoplastyen_US
dc.subjectfacial plastic surgeryen_US
dc.titleLong-Term Inflammatory Response to Liquid Injectable Silicone, Cartilage, and Silicone Sheeten_US
dc.typearticleen_US

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