{"title":"Morphology-dependent titanium dioxide nanoparticle-induced keratinocyte toxicity and exacerbation of allergic contact dermatitis.","authors":"Brian C Palmer, Lisa A DeLouise","doi":"10.24966/tcr-3735/100019","DOIUrl":null,"url":null,"abstract":"<p><p>Titanium dioxide (TiO<sub>2</sub>) nanoparticles are commonly found in consumer products, such as sunscreens, and human dermal exposures are relatively high. Research suggests potential differences in the toxicity of anatase and rutile crystalline forms of TiO<sub>2</sub>. Additionally, transition metal dopants are frequently used to enhance physicochemical properties of TiO<sub>2</sub>, and the toxicity of these nanoparticles are not extensively studied. Therefore, this work examined the keratinocyte toxicity and <i>in vivo</i> skin allergy responses after treatment with 30 nm anatase, 30 nm rutile, or <100 nm Mn-doped TiO<sub>2</sub> nanoparticles. After a 24-hour exposure, there were no differences in keratinocyte cytotoxicity; however, Mn-doped TiO<sub>2</sub> nanoparticles induced significant <i>in vitro</i> ROS generation and <i>in vivo</i> skin swelling responses in a model of allergic contact dermatitis.</p>","PeriodicalId":93103,"journal":{"name":"HSOA journal of toxicology : current research","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643926/pdf/nihms-1640696.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HSOA journal of toxicology : current research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24966/tcr-3735/100019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/6/17 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Titanium dioxide (TiO2) nanoparticles are commonly found in consumer products, such as sunscreens, and human dermal exposures are relatively high. Research suggests potential differences in the toxicity of anatase and rutile crystalline forms of TiO2. Additionally, transition metal dopants are frequently used to enhance physicochemical properties of TiO2, and the toxicity of these nanoparticles are not extensively studied. Therefore, this work examined the keratinocyte toxicity and in vivo skin allergy responses after treatment with 30 nm anatase, 30 nm rutile, or <100 nm Mn-doped TiO2 nanoparticles. After a 24-hour exposure, there were no differences in keratinocyte cytotoxicity; however, Mn-doped TiO2 nanoparticles induced significant in vitro ROS generation and in vivo skin swelling responses in a model of allergic contact dermatitis.