Dermatotoxicity of Cutting Fluid Mixtures:In VitroandIn VivoStudies
- 1 January 2006
- journal article
- research article
- Published by Taylor & Francis in Cutaneous and Ocular Toxicology
- Vol. 25 (4) , 235-247
- https://doi.org/10.1080/15569520601013137
Abstract
Cutting fluids are widely used in the metal-machining industry to lubricate and reduce heat generation when metals are cut by a metal-cutting tool. These cutting fluids have caused occupational irritant contact dermatitis (OICD), and many of the additives used in these cutting fluid mixtures are thought to be responsible for OICD in workers. The purpose of this study was to assess single or various combinations of these additives in initiating the OICD response following an acute 8-hour exposure in porcine skin in vivo and in vitro using the isolated perfused porcine skin flap (IPPSF) and human epidermal keratinocytes (HEK). Pigs (n = 4) were exposed to 5% mineral oil (MO) or 5% polyethylene glycol (PEG) aqueous mixtures containing various combinations of 2% triazine (TRI), 5% triethanolamine (TEA), 5% linear alkylbenzene sulfonate (LAS), or 5% sulfurized ricinoleic acid (SRA). Erythema and edema were evaluated and skin biopsies for histopathology were obtained at 4 and 8 hours. IPPSFs (n = 4) were exposed to control MO or PEG mixtures and complete MO or PEG mixtures, and perfusate samples were collected hourly to determine interleukin- (IL-) 8 release. The only significant (p < 0.05) mixture effects observed in IPPSFs were with SRA + MO that caused an increase in IL-8 release after 1 or 2 hours' exposure. In vivo exposure to TRI alone appeared to increase erythema, edema, and dermal inflammation compared to the other additives, while SRA alone was least likely to initiate a dermal inflammatory response. In 2-component mixture exposures, the presence of TRI appeared to increase the dermal inflammatory response at 4 and 8 hours especially with the PEG mixtures. In the 3- and 4-component mixtures, MO mixtures are more likely to incite an inflammatory response than PEG mixtures. TRI exhibited the highest toxicity toward HEK, which correlates well to the in vivo irritation and morphology results. In summary, these preliminary studies suggest that the biocide, TRI, is the more potent of the 4 performance additives in causing dermal irritation, and this may vary depending on whether the worker is exposed to a synthetic (PEG)- or MO-based fluid. These findings will however require further clinical studies to validate these acute dermal effects as well as human cumulative irritation following exposure to similar cutting fluid formulations in the workplace.Keywords
This publication has 26 references indexed in Scilit:
- Dermal Disposition of Triazine in Cutting Fluid MixturesJournal of Toxicology- Cutaneous and Ocular Toxicology, 2003
- DERMAL TOXICITY OF LINEAR ALKYLBENZENE SULPHONATE AND NICKEL IN GUINEA PIGSJournal of Toxicology- Cutaneous and Ocular Toxicology, 2001
- DERMAL AND SYSTEMIC TOXICITY AFTER APPLICATION OF SEMISYNTHETIC METAL-WORKING FLUIDS IN B6C3F1 MICEJournal of Toxicology and Environmental Health, Part A, 2000
- Identification of early biomarkers of inflammation produced by keratinocytes exposed to jet fuels jet A, JP-8, and JP-8(100)Journal of Biochemical and Molecular Toxicology, 2000
- Keratinocyte-Derived Proinflammatory Key Mediators and Cell Viability as in Vitro Parameters of Irritancy: A Possible Alternative to the Draize Skin Irritation TestToxicology and Applied Pharmacology, 1994
- Causes of death among workers in a bearing manufacturing plantAmerican Journal of Industrial Medicine, 1988
- The isolated perfused porcine skin flap (IPPSF) I. A novel in vitro model for percutaneous absorption and cutaneous toxicology studiesFundamental and Applied Toxicology, 1986
- Studies on the acute toxicity, primary irritancy and genotoxic potential of 1,3,5-triacryloylhexahydro-s-triazine (TAHT)Toxicology, 1986
- Effect of Fatty Acids and Alcohols on the Penetration of Acyclovir Across Human Skin in VitroJournal of Pharmaceutical Sciences, 1985
- Lipstick dermatitis caused by ricinoleic acidContact Dermatitis, 1983