Penetration Deep into Tissues of Reactive Oxygen Species Generated in Floating-Electrode Dielectric Barrier Discharge (FE-DBD): in Vitro Agarose Gel Model Mimicking an Open Wound
{"title":"Penetration Deep into Tissues of Reactive Oxygen Species Generated in Floating-Electrode Dielectric Barrier Discharge (FE-DBD): in Vitro Agarose Gel Model Mimicking an Open Wound","authors":"D. Dobrynin, G. Fridman, G. Friedman, A. Fridman","doi":"10.1615/PLASMAMED.2013006218","DOIUrl":null,"url":null,"abstract":"In this manuscript we present an in vitro model based on agarose gel that can be used to simulate a dirty, oily, bloody, and morphologically complex surface of, for example, an open wound. We show this models effectiveness in simulating depth of penetration of reactive species generated in plasma deep into tissue of a rat and confirm the penetration depths with agarose gel model. We envision that in the future such a model could be used to study plasma discharges (and other modalities) and minimize the use of live animals: plasma can be optimized on the agarose gel wound model and then finally verified using an actual wound.","PeriodicalId":360136,"journal":{"name":"arXiv: Biological Physics","volume":"132 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"33","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv: Biological Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1615/PLASMAMED.2013006218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 33
Abstract
In this manuscript we present an in vitro model based on agarose gel that can be used to simulate a dirty, oily, bloody, and morphologically complex surface of, for example, an open wound. We show this models effectiveness in simulating depth of penetration of reactive species generated in plasma deep into tissue of a rat and confirm the penetration depths with agarose gel model. We envision that in the future such a model could be used to study plasma discharges (and other modalities) and minimize the use of live animals: plasma can be optimized on the agarose gel wound model and then finally verified using an actual wound.