Di(2-ethylhexyl)phthalate (DEHP) metabolites in human urine and serum after a single oral dose of deuterium-labelled DEHP

被引:305
作者
Koch, HM
Bolt, HM
Angerer, J
机构
[1] Univ Erlangen Nurnberg, Inst & Outpatient Clin Occupat Social & Enviornm, D-91054 Erlangen, Germany
[2] Univ Dortmund, Inst Occupat Physiol, Leibniz Res Ctr Working Enviornm & Human Factors, D-44139 Dortmund, Germany
关键词
metabolism; urine; serum; di(2-ethylhexyl)phthalate (DEHP); mono(2-ethyl-5-hydroxyhexyl)phthalate (5OH-MEHP); mono(2-ethyl-5-oxohexyl)phthalate (5oxo-MEHP); mono(2-ethylhexyl)phthalate (MEHP);
D O I
10.1007/00204-003-0522-3
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Human metabolism of di(2-ethylhexyl)phthalate (DEHP) was studied after a single oral dose of 48.1 mg to a male volunteer. To avoid interference by background exposure the D4-ring-labelled DEHP analogue was dosed. Excretion of three metabolites, mono(2-ethyl-5-hydroxyhexyl)phthalate (5OH-MEHP), mono(2-ethyl-5-oxohexyl)phthalate (5oxo-MEHP) and mono(2-ethylhexyl)phthalate (MEHP), was monitored for 44 h in urine and for 8 h in serum. Peak concentrations of all metabolites were found in serum after 2 h and in urine after 2 h (MEHP) and after 4 h (5OH-MEHP and 5oxo-MEHP). While the major metabolite in serum was MEHP, the major metabolite in urine was 5OH-MEHP, followed by 5oxo-MEHP and MEHP. Excretion in urine followed a multi-phase elimination model. After an absorption and distribution phase of 4 to 8 h, half-life times of excretion in the first elimination phase were approximately 2 h with slightly higher half-life times for 5OH- and 5oxo-MEHP. Half-life times in the second phase-beginning 14 to 18 h post dose-were 5 h for MEHP and 10 h for 5OH-MEHP and 5oxo-MEHP. In the time window 36 to 44 h, no decrease in excreted concentrations of 5OH- and 5oxo-MEHP was observed. In the first elimination phase (8 to 14 h post dose), mean excretion ratios of MEHP to 5oxo-MEHP and MEHP to 5OH-MEHP were 1 to 1.8 and 1 to 3.1. In the second elimination phase up to 24 h post dose mean excretion ratios of MEHP to 5oxo-MEHP to 5OH-MEHP were 1 to 5.0 to 9.3. The excretion ratio of 5OH-MEHP to 5oxo-MEHP remained constant through time at 1.7 in the mean. After 44 h, 47% of the DEHP dose was excreted in urine, comprising MEHP (7.3%), 5OH-MEHP (24.7%) and 5oxo-MEHP (14.9%).
引用
收藏
页码:123 / 130
页数:8
相关论文
共 43 条
[1]   Modulation of rat Leydig cell steroidogenic function by di(2-ethylhexyl)phthalate [J].
Akingbemi, BT ;
Youker, RT ;
Sottas, CM ;
Ge, RS ;
Katz, E ;
Klinefelter, GR ;
Zirkin, BR ;
Hardy, MP .
BIOLOGY OF REPRODUCTION, 2001, 65 (04) :1252-1259
[2]   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
[3]   A biomarker approach to measuring human dietary exposure to certain phthalate diesters [J].
Anderson, WAC ;
Castle, L ;
Scotter, MJ ;
Massey, RC ;
Springall, C .
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2001, 18 (12) :1068-1074
[4]   Oral toxicity of bis(2-ethylhexyl) phthalate during pregnancy and suckling in the Long-Evans rat [J].
Arcadi, FA ;
Costa, C ;
Imperatore, C ;
Marchese, A ;
Rapisarda, A ;
Salemi, M ;
Trimarchi, GR ;
Costa, G .
FOOD AND CHEMICAL TOXICOLOGY, 1998, 36 (11) :963-970
[5]  
ATSDR Agency for Toxic Substances and Disease Registry, 1993, ATDRTP9205 US DEP HH, P171
[6]   Assessing human exposure to phthalates using monoesters and their oxidized metabolites as biomarkers [J].
Barr, DB ;
Silva, MJ ;
Kato, K ;
Reidy, JA ;
Malek, NA ;
Hurtz, D ;
Sadowski, M ;
Needham, LL ;
Calafat, AM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (09) :1148-1151
[7]   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
[8]  
Butte W, 2001, GEFAHRST REINHALT L, V61, P19
[9]   Evaluation of reproductive development following intravenous and oral exposure to DEHP in male neonatal rats [J].
Cammack, JN ;
White, RD ;
Gordon, D ;
Gass, J ;
Hecker, L ;
Conine, D ;
Bruen, US ;
Friedman, M ;
Echols, C ;
Yeh, TY ;
Wilson, DM .
INTERNATIONAL JOURNAL OF TOXICOLOGY, 2003, 22 (03) :159-174
[10]  
CDC (Centers for Disease Control and Prevention), 2003, NCEH PUB