White Mineral Oils

2008 ◽  
pp. 210-210-5
Author(s):  
SJ Rand ◽  
CM Copeland
Keyword(s):  
Mineral Oils ◽  
White Mineral

White Mineral Oils

2010 ◽  
pp. 184-184-5
Author(s):  
Salvatore J. Rand ◽  
C. Monroe Copeland
Keyword(s):  
Mineral Oils ◽  
White Mineral

Results of Chronic Dietary Toxicity Studies of High Viscosity (P70H and P100H) White Mineral Oils in Fischer 344 Rats

2004 ◽  
Vol 32 (4) ◽  
pp. 439-447 ◽  
Author(s):  
Gary W. Trimmer ◽  
James J. Freeman ◽  
R. A. J. Priston ◽  
Jan Urbanus
Keyword(s):  
High Viscosity ◽  
Female Rats ◽  
Fischer 344 Rats ◽  
Mesenteric Lymph Nodes ◽  
Mineral Oils ◽  
Fischer 344 ◽  
Mesenteric Lymph ◽  
Dietary Concentration ◽  
Study Results ◽  
White Mineral

Two-year dietary studies were conducted to determine the chronic toxicity and its reversibility, and the carcinogenicity of P70(H) and P100(H) white mineral oils in Fischer-344 rats (F-344). The studies were identical in design and followed the Organization for Economic Cooperation and Development, Guidelines for Testing Chemicals, Guideline 453, 1981. Additional endpoints evaluated were: (1) extent of mineral hydrocarbon deposition in liver, kidneys, mesenteric lymph nodes, and spleen of female rats at 3, 6, 12, 18 and 24 months, and (2) reversibility of effects following cessation of exposure. Dietary concentration were 60, 120, 240, and 1, 200 mg/kg/day, adjusted periodically to account for bodyweight changes. Study results were consistent with preceding subchronic studies. No treatment-related mortality, neoplastic lesions, or changes in clinical health, hematology, serum chemistry, or urine chemistry were evident in any group administered either white oil. Statistically significant higher food consumption was noted in the 1, 200 mg/kg group males and females exposed to either white oil and statistically significant higher body weights were noted in the 1, 200-mg/kg males during the latter portion of the P100(H) study. Higher mesenteric lymph node weights were accompanied by increased severity of infiltrating histiocytes. This occurred to a greater extent with the P70(H) than the P100(H) oil. No other histopathology of significance was observed. Mineral hydrocarbons were detected in the liver following exposure to either oil. Maximal concentrations of mineral hydrocarbons in the liver were similar with both oils but occurred more rapidly with the P70(H) oil. Liver mineral hydrocarbon content returned to near-background levels during the reversibility phase. In conclusion, lifetime exposer of F344 rats to P70(H) and P100(H) white oils resulted in only minimal findings and with no consequence to clinical health. Thus, under the conditions of these studies, the No Observable Adverse Effect Level (NOAEL) for these studies was considered to be 1, 200 mg/kg/day.

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