Use of a Statistical Model to Predict the Potential for Repeated Dose and Developmental Toxicity of Dermally Administered Crude Oil and Relation to Reproductive Toxicity

Petroleum (commonly called crude oil) is a complex substance primarily composed of hydrocarbon constituents. Based on the results of previous toxicological studies as well as occupational experience, the principal acute toxicological hazards are those associated with exposure by inhalation to volatile hydrocarbon constituents and hydrogen sulfide, and chronic hazards are associated with inhalation exposure to benzene and dermal exposure to polycyclic aromatic compounds. The current assessment was an attempt to characterize the potential for repeated dose and/or developmental effects of crude oils following dermal exposures and to generalize the conclusions across a broad range of crude oils from different sources. Statistical models were used to predict the potential for repeated dose and developmental toxicity from compositional information. The model predictions indicated that the empirical data from previously tested crude oils approximated a “worst case” situation, and that the data from previously tested crude oils could be used as a reasonable basis for characterizing the repeated dose and developmental toxicological hazards of crude oils in general.

[1]  H. Bartsch,et al.  International Agency for Research on Cancer. , 1969, WHO chronicle.

[2]  Myron A. Mehlman,et al.  Advances in modern environmental toxicology , 1980 .

[3]  H. Enoch,et al.  Comparative study of the genotoxic properties of Eastern and Western U.S. shale oils, crude petroleum, and coal-derived oil. , 1982, Mutation research.

[4]  K S Crump,et al.  A new method for determining allowable daily intakes. , 1984, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[5]  S. Cragg,et al.  Lack of concordance of the Salmonella/microsome assay with the mouse dermal carcinogenesis bioassay for complex petroleum hydrocarbon mixtures. , 1985, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[6]  S. Cragg,et al.  Lack of concordance of the Salmonella/microsome assay with the mouse dermal carcinogenesis bioassay for complex petroleum hydrocarbon mixtures. , 1985, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[7]  W. Stubblefield,et al.  Evaluation of the dermal carcinogenic potential of tar sands bitumen-derived liquids. , 1986, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[8]  S. Khan,et al.  Embryotoxic evaluation of a Prudhoe Bay crude oil in rats. , 1987, Toxicology letters.

[9]  C. Mackerer,et al.  Correlation of mutagenic and dermal carcinogenic activities of mineral oils with polycyclic aromatic compound content. , 1988, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[10]  Correlation of mutagenic and dermal carcinogenic activities of mineral oils with polycyclic aromatic compound content. , 1988 .

[11]  M. Cooke,et al.  PAH-X: Polynuclear aromatic hydrocarbons: A decade of progress , 1988 .

[12]  F. Leighton The systemic toxicity of Prudhoe Bay crude and other petroleum oils to CD-1 mice , 1990, Archives of environmental contamination and toxicology.

[13]  C. Mackerer,et al.  Correlation of systemic and developmental toxicities with chemical component classes of refinery streams. , 1994, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[14]  A. Hoberman,et al.  Developmental toxicity study of clarified slurry oil (CSO) in the rat. , 1995, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[15]  A. Hoberman,et al.  Reproductive Toxicity Study of Clarified Slurry Oil in the Rat , 1995 .

[16]  C. Mackerer,et al.  Systemic toxicity of dermally applied crude oils in rats. , 1997, Journal of toxicology and environmental health.

[17]  C. Mackerer,et al.  Developmental toxicity of dermally applied crude oils in rats. , 1997, Journal of toxicology and environmental health.

[18]  Michigan.,et al.  Toxicological profile for dichloropropenes , 2008 .

[19]  M Pelekis,et al.  Evaluation of subchronic toxicity data using the benchmark dose approach. , 2001, Regulatory toxicology and pharmacology : RTP.

[20]  O. Orisakwe,et al.  Testicular toxicity of Nigerian bonny light crude oil in male albino rats. , 2004, Reproductive toxicology.

[21]  C.-H. Selene J. Chou,et al.  Toxicological profile for hydrogen sulfide , 2006 .

[22]  Deborah Cussen,et al.  Mercury in crude oil processed in the United States (2004). , 2007, Environmental science & technology.

[23]  I. Obidike,et al.  Testicular morphology and cauda epididymal sperm reserves of male rats exposed to Nigerian Qua Iboe Brent crude oil , 2007, Journal of veterinary science.

[24]  M. Witko,et al.  Sixth International Symposium. Effects of surface heterogeneity in adsorption and catalysis on solids—ISSHAC VI, Zakopane, Poland, 28th August-2nd September 2006 , 2007 .

[25]  Mark J Nicolich,et al.  Assessing the mammalian toxicity of high-boiling petroleum substances under the rubric of the HPV program. , 2013, Regulatory toxicology and pharmacology : RTP.

[26]  J. J. Freeman,et al.  A GHS-consistent approach to health hazard classification of petroleum substances, a class of UVCB substances. , 2013, Regulatory toxicology and pharmacology : RTP.

[27]  Mark J Nicolich,et al.  The relationship between developmental toxicity and aromatic-ring class profile of high-boiling petroleum substances. , 2013, Regulatory toxicology and pharmacology : RTP.

[28]  Mark J Nicolich,et al.  The relationship between repeat-dose toxicity and aromatic-ring class profile of high-boiling petroleum substances. , 2013, Regulatory toxicology and pharmacology : RTP.

[29]  Mark J Nicolich,et al.  The development of statistical models to determine the relationship between aromatic-ring class profile and repeat-dose and developmental toxicities of high-boiling petroleum substances. , 2013, Regulatory toxicology and pharmacology : RTP.