{"title":"三乙醇胺经人体皮肤体外吸收的研究","authors":"M. Kraeling, R. Bronaugh","doi":"10.1081/CUS-120022754","DOIUrl":null,"url":null,"abstract":"The human skin penetration of triethanolamine (TEA) was measured using in vitro diffusion cell techniques. [14C]TEA was applied to viable skin in an oil-in-water emulsion containing TEA stearate as an emulsifying agent to simulate cosmetic exposure. The percent of the applied dose of TEA absorbed into the receptor fluid was similar with both 1% and 5% TEA formulations. Absorption of TEA was reduced by lowering the pH of the formulation, presumably due to the increased ionization of TEA. Absorption of TEA into the receptor fluid (1% formulation, pH 7.0) was 0.43% of the applied dose in a 24 h study. Substantial amounts of TEA remained in the skin at the end of the study (9.4% of dose), but only minimal amounts diffused into the receptor fluid when the collection time was extended to 72 h in separate studies. The amount of TEA remaining in skin at the end of the 24 h studies should not be included in estimates of systemic absorption.","PeriodicalId":17547,"journal":{"name":"Journal of Toxicology-cutaneous and Ocular Toxicology","volume":"1 1","pages":"137 - 145"},"PeriodicalIF":0.0000,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"In Vitro Absorption of Triethanolamine Through Human Skin\",\"authors\":\"M. Kraeling, R. Bronaugh\",\"doi\":\"10.1081/CUS-120022754\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The human skin penetration of triethanolamine (TEA) was measured using in vitro diffusion cell techniques. [14C]TEA was applied to viable skin in an oil-in-water emulsion containing TEA stearate as an emulsifying agent to simulate cosmetic exposure. The percent of the applied dose of TEA absorbed into the receptor fluid was similar with both 1% and 5% TEA formulations. Absorption of TEA was reduced by lowering the pH of the formulation, presumably due to the increased ionization of TEA. Absorption of TEA into the receptor fluid (1% formulation, pH 7.0) was 0.43% of the applied dose in a 24 h study. Substantial amounts of TEA remained in the skin at the end of the study (9.4% of dose), but only minimal amounts diffused into the receptor fluid when the collection time was extended to 72 h in separate studies. The amount of TEA remaining in skin at the end of the 24 h studies should not be included in estimates of systemic absorption.\",\"PeriodicalId\":17547,\"journal\":{\"name\":\"Journal of Toxicology-cutaneous and Ocular Toxicology\",\"volume\":\"1 1\",\"pages\":\"137 - 145\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Toxicology-cutaneous and Ocular Toxicology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1081/CUS-120022754\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Toxicology-cutaneous and Ocular Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/CUS-120022754","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In Vitro Absorption of Triethanolamine Through Human Skin
The human skin penetration of triethanolamine (TEA) was measured using in vitro diffusion cell techniques. [14C]TEA was applied to viable skin in an oil-in-water emulsion containing TEA stearate as an emulsifying agent to simulate cosmetic exposure. The percent of the applied dose of TEA absorbed into the receptor fluid was similar with both 1% and 5% TEA formulations. Absorption of TEA was reduced by lowering the pH of the formulation, presumably due to the increased ionization of TEA. Absorption of TEA into the receptor fluid (1% formulation, pH 7.0) was 0.43% of the applied dose in a 24 h study. Substantial amounts of TEA remained in the skin at the end of the study (9.4% of dose), but only minimal amounts diffused into the receptor fluid when the collection time was extended to 72 h in separate studies. The amount of TEA remaining in skin at the end of the 24 h studies should not be included in estimates of systemic absorption.