Effects of short‐term high‐dose and low‐dose dermal exposure to Jet A, JP‐8 and JP‐8 + 100 jet fuels

Occupational and environmental exposures to jet fuel recently have become a source of public and regulatory concern. This study investigates the cutaneous toxicity of three fuels used in both civilian and military aircraft. Pigs, an accepted animal model for human skin, were exposed to low‐dose (25 µl or 7.96 µl cm−2) or high‐dose (335 µl or 67 µl cm−2) Jet A, JP‐8 and JP‐8 + 100 under occluded (Hill Top® chamber or cotton fabric) and non‐occluded conditions for 5 h, 24 h and 5 days. To mimic occupational exposure, fuel‐soaked fabric (high dose) was used. Erythema, edema, transepidermal water loss (TEWL) and epidermal thickness were quantified. High‐dose fabric occluded sites had slight erythema at 5 h with increased erythema at 5 days. No erythema was noted in any of the occluded (Hill Top) or non‐occluded sites at any of the time points. Morphological assessments depicted slight intracellular epidermal edema at all time points. An increase in change in TEWL (ΔTEWL) was observed at the 5‐h and 24‐h fabric and Hill Top occluded treatments and a decrease at the 5‐day fabric and Hill Top occluded sites. In all 5‐day JP‐8 + 100 fabric sites, intracorneal microabscesses filled with inflammatory cells were observed. Epidermal thickening was significant (P < 0.05) in all three jet fuels at the high‐dose fabric sites, with JP‐8 + 100 being the thickest. The epidermal rete peg depth increased significantly (P < 0.05) at 24 h and 5 days with Jet A, JP‐8, and JP‐8 + 100 in the fabric sites. No significant differences were noted in the 5‐day non‐occluded fabric and Hill Top occluded and non‐occluded sites. Jet fuel JP‐8 + 100 tended to have the greatest proliferative response. In conclusion, the high‐dose fabric‐soaked exposure at 5 days to Jet A, JP‐8 and JP‐8 + 100 fuels caused the greatest increase in cutaneous erythema, edema, epidermal thickness and rete peg depth compared with high‐dose non‐occluded or low‐dose exposure under Hill Top occluded and non‐occluded conditions. Copyright © 2001 John Wiley & Sons, Ltd.

[1]  Wade H. Weisman,et al.  Assessment of skin absorption and penetration of JP-8 jet fuel and its components. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[2]  R. Bronaugh,et al.  Methods for in vitro percutaneous absorption studies. II. Animal models for human skin. , 1982, Toxicology and applied pharmacology.

[3]  S. Ullrich,et al.  Dermal application of JP-8 jet fuel induces immune suppression. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[4]  V. Brown,et al.  SKIN ARGINASE ACTIVITY AS A MEASURE OF SKIN CHANGE UNDER THE INFLUENCE OF SOME ALKANES AND ALKENES * , 1970, The British journal of dermatology.

[5]  N. Monteiro-Riviere,et al.  Identification of early biomarkers of inflammation produced by keratinocytes exposed to jet fuels jet A, JP‐8, and JP‐8(100) , 2000, Journal of biochemical and molecular toxicology.

[6]  A Bhattacharya,et al.  Effect of chronic low-level exposure to jet fuel on postural balance of US Air Force personnel. , 1997, Journal of occupational and environmental medicine.

[7]  R A Scala,et al.  Dermal carcinogenic activity of petroleum-derived middle distillate fuels. , 1988, Toxicology.

[8]  J. Riviere,et al.  Membrane transport of naphthalene and dodecane in jet fuel mixtures , 2000 .

[9]  M. Sharratt,et al.  Early changes produced in mouse skin by the application of three middle distillates. , 1988, Cancer letters.

[10]  D. Stenger,et al.  INVESTIGATION OF IN VITRO TOXICITY OF JET FUELS JP-8 AND JET A , 2000, Drug and chemical toxicology.

[11]  J J Freeman,et al.  The role of dermal irritation in the skin tumor promoting activity of petroleum middle distillates. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[12]  J. J. Freeman,et al.  Short-term biomarkers of tumor promotion in mouse skin treated with petroleum middle distillates. , 1998, Toxicological sciences : an official journal of the Society of Toxicology.

[13]  J. Sicé Tumor-promoting activity of n-alkanes and 1-alkanols , 1966 .

[14]  R. D. White,et al.  Refining and blending of aviation turbine fuels. , 1999, Drug and chemical toxicology.

[15]  John Pfaff,et al.  Inhalation exposure to jp‐8 jet fuel alters pulmonary function and substance p levels in fischer 344 rats , 1995, Journal of applied toxicology : JAT.

[16]  R. Robledo,et al.  Immunotoxicological Effects of Jp-8 Jet Fuel Exposure , 1997, Toxicology and industrial health.

[17]  H. Tagami,et al.  Kerosine dermatitis. Factors affecting skin irritability to kerosine. , 1973, Dermatologica.

[18]  R. Robledo,et al.  Short-Term Exposure To Jp-8 Jet Fuel Results in Longterm Immunotoxicity , 1997 .

[19]  J E Riviere,et al.  Dermal absorption and distribution of topically dosed jet fuels jet-A, JP-8, and JP-8(100). , 1999, Toxicology and applied pharmacology.

[20]  R Schwarz,et al.  The Skin of Domestic Mammals as a Model for the Human Skin, with Special Reference to the Domestic Pig1 , 1978 .

[21]  C L Alden,et al.  A 90-Day Continuous Vapor Inhalation Toxicity Study of JP-8 Jet Fuel Followed by 20 or 21 Months of Recovery in Fischer 344 Rats and C57BL/6 Mice , 1991, Toxicologic pathology.

[22]  G N Carlton,et al.  Exposures to jet fuel and benzene during aircraft fuel tank repair in the U.S. Air Force. , 2000, Applied occupational and environmental hygiene.

[23]  N. Monteiro-Riviere,et al.  The Pig as a Model for Cutaneous Pharmacology and Toxicology Research , 1996 .

[24]  R D Phillips,et al.  A 90-Day Toxicity Study of the Effects of Petroleum Middle Distillates on the Skin of C3H Mice a , 1990, Toxicology and industrial health.

[25]  R. Robledo,et al.  Effects of short-term JP-8 jet fuel exposure on cell-mediated immunity , 2000, Toxicology and industrial health.

[26]  N. Monteiro-Riviere,et al.  Cytokine induction as a measure of cutaneous toxicity in primary and immortalized porcine keratinocytes exposed to jet fuels, and their relationship to normal human epidermal keratinocytes. , 2001, Toxicology letters.

[27]  C R Clark,et al.  Comparative Dermal Carcinogenesis of Shale and Petroleum-Derived Distillates , 1988, Toxicology and industrial health.