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

Journal of Applied Toxicology

Volumn 21, Issue 6, 2001, Pages 485-494

  Monteiro Riviere, Nancy ^a   Inman, Alfred ^a   Riviere, Jim ^a  

^a NORTH CAROLINA STATE UNIVERSITY   (United States)

Author keywords

Dermatopathology; Dermatotoxicity; Hydrocarbon fuels; Jet A; Jet fuels; JP 8; JP 8+100; Pig; Skin

Indexed keywords

FUEL;

ABSCESS; AIRCRAFT; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARMY; ARTICLE; CELL PROLIFERATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; CORNEA; EDEMA; ENVIRONMENTAL EXPOSURE; EPIDERMIS; ERYTHEMA; FEMALE; INFLAMMATORY CELL; MORPHOLOGY; NONHUMAN; OCCUPATIONAL EXPOSURE; PRIORITY JOURNAL; SKIN TOXICITY; SWINE; THICKNESS; WATER LOSS;

ADMINISTRATION, CUTANEOUS; AIRCRAFT; ANIMALS; CELL DIVISION; CLOTHING; EDEMA; EPIDERMIS; ERYTHEMA; FEMALE; HUMANS; HYDROCARBONS; KEROSENE; OCCUPATIONAL EXPOSURE; SWINE; WATER-ELECTROLYTE BALANCE;

ANIMALIA; GOSSYPIUM HIRSUTUM; SUS SCROFA;

EID: 0035199646     PISSN: 0260437X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jat.785     Document Type: Article

References (36)

1. Effects of short-term JP-8 jet fuel exposure on cell-mediated immunity. Toxicol
2. Pollutant emission characteristics of future aviation jet fuels
3. Exposures to jet fuel and benzene during aircraft fuel tank repair in the U.S. Air Force
4. Refining and blending of aviation turbine fuels
5. Immunotoxicological effects of JP-8 jet fuel exposure
6. Short-term exposure to JP-8 jet fuel results in longterm immunotoxicity
7. 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 C56BL/6 mice
8. Dermal application of JP-8 jet fuel induces immune suppression
9. Effect of chronic low-level exposure to jet fuel on postural balance of US Air force personnel
10. Investigation of in vitro toxicology of jet fuels JP-8 and Jet A
11. Dermal absorption and distribution of topically dosed jet fuels Jet-A, JP-8, and JP-8 (100)
12. Assessment of skin absorption and penetration of JP-8 jet fuel and its components
13. Comparative dermal carcinogenesis of shale and petroleum-derived distillates
14. The role of dermal irritation in the skin tumor promoting activity of petroleum middle distillates
15. Short-term biomarkers of tumor promotion in mouse skin treated with petroleum middle distillates
16. Kerosine dermatitis. Factors affecting skin irritability to kerosine
17. A 90-day toxicity study of the effects of petroleum middle distillates on the skin of C3H mice
18. Early changes produced in mouse skin by the application of three middle distillates
19. Identification of early biomarkers of inflammation produced by keratinocytes exposed to jet fuels Jet A, JP-8, and JP-8 (100)
20. The skin of domestic mammals as a model for the human skin with special reference to the domestic pig
21. Ultrastructure of the integument of the domestic pig (Sus scrofa) from one through fourteen weeks of age
22. Ultrastructural evaluation of the porcine integument
23. The integument
24. The integument
25. The pig as a model for cutaneous pharmacology and toxicology research
26. Methods for in vitro percutaneous absorption studies. II. Animal models for human skin
27. Animal models for percutaneous absorption
28. Inhalation exposure to JP-8 jet fuels alters pulmonary function and substance P levels in Fischer 344 rats
29. Dermal carcinogenic activity of petroleum-derived middle distillate fuels
30. Tumor-promoting activity of n-alkanes and I-alkanols
31. Skin arginase activity as a measure of skin change under the influence of some alkanes and alkenes
32. Membrane transport of naphthalene and dodecane in jet fuel mixtures
33. Aliphatic hydrocarbons induce the release of interleukin-8 from normal human epidermal keratinocytes: Delivery of hydrocarbons to cell culture via complexation with α-cyclodextrin. Toxicol
34. 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