Toxicokinetic relationship between di(2-ethyl hexyl) phthalate (DEHP) and mono (2-ethyl hexyl) phthalate in rats

被引:22
作者
Koo, Hyuin Jung [1 ]
Lee, Byung Mu [1 ]
机构
[1] Sungkyunkwan Univ, Div Toxicol, Coll Pharm, Suwon 440746, Kyonggi Do, South Korea
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2007年 / 70卷 / 5-6期
关键词
D O I
10.1080/15287390600882150
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The toxicokinetic relationship between di(2-ethylhexyl) phthalate (DEHP) and mono(2-ethylhexyl) phthalate (MEHP), a major metabolite of DEHP, was investigated in Sprague-Dawley rats orally treated with a single dose of C-14-DEHP. Urinary excretion 4 total C-14-DEHP and of its metabolites was followed by liquid scintillation counting (LSC). Concentrations of DEHP and MEHP were determined 6, 24, and 48 h after treatment in rat serum and 6, 12, 24, and 48 h after treatment in urine by high-performance liquid chromatography (HPLC). After 24 h, peak concentrations of MEHP in both urine and serum were observed in animals treated with 40, 200, or 1000 ling DEHP/kg. HPLC showed that general toxicokinetic parameters, such as Tmax (h), Cmax (mu g/ml), Ke (1/h), and AUC (mu g-h/ml/) were greater for MEHP than DEHP in both urine and serum. In contrast, the half-lives (t(1/2) [h]) of DEHP were greater than those of MEHP. The AUC ratios between DEHP and MEHP were relatively smaller in serum than in urine, suggesting the important role of urinary DEHP data for exposure assessment of DEHP. The toxicokinetic relationship between DEHP and MEHP in rats suggests that DEHP exposure assessment should be based on DEHP and MEHP in urine and serum for risk assessment applications.
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页码:383 / 387
页数:5
相关论文
共 21 条
[1]  
*AG TOX SUBST DIS, 1993, TOX PROF DI2 ETH PHT
[2]  
*AG TOX SUBST DIS, 1999, TOX PROF DI N BUT UP
[3]   PHARMACOKINETICS, INTERACTIONS WITH MACROMOLECULES AND SPECIES-DIFFERENCES IN METABOLISM OF DEHP [J].
ALBRO, PW ;
CORBETT, JT ;
SCHROEDER, JL ;
JORDAN, S ;
MATTHEWS, HB .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1982, 45 (NOV) :19-25
[4]  
[Anonymous], TOX PROF DIETH PHTHA
[5]   Levels of seven urinary phthalate metabolites in a human reference population [J].
Blount, BC ;
Silva, MJ ;
Caudill, SP ;
Needham, LL ;
Pirkle, JL ;
Sampson, EJ ;
Lucier, GW ;
Jackson, RJ ;
Brock, JW .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 (10) :979-982
[6]  
*CDCP, 2003, 2 CDCP NAT CTR ENV H
[7]  
*CHEM MAN ASS, 1999, 999484 FR CHEM MAN A
[8]   Toxicological characteristics of endocrine-disrupting chemicals: Developmental toxicity, carcinogenicity, and mutagenicity [J].
Choi, SM ;
Yoo, SD ;
Lee, BM .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS, 2004, 7 (01) :1-32
[9]   Chronic peroxisome proliferation and hepatomegaly associated with the hepatocellular tumorigenesis of di(2-ethylhexyl)phthalate and the effects of recovery [J].
David, RM ;
Moore, MR ;
Cifone, MA ;
Finney, DC ;
Guest, D .
TOXICOLOGICAL SCIENCES, 1999, 50 (02) :195-205
[10]   Chronic toxicity of di(2-ethylhexyl)phthalate in rats [J].
David, RM ;
Moore, MR ;
Finney, DC ;
Guest, D .
TOXICOLOGICAL SCIENCES, 2000, 55 (02) :433-443