Modeling Human Exposure to Phthalate Esters: A Comparison of Indirect and Biomonitoring Estimation Methods

被引:90
作者
Clark, Kathryn E. [1 ]
David, Raymond M. [2 ]
Guinn, Richard [4 ]
Kramarz, Kurt W. [3 ]
Lampi, Mark A. [5 ]
Staples, Charles A. [6 ]
机构
[1] BEC Technol Inc, Aurora, ON, Canada
[2] BASF Corp, Florham Pk, NJ USA
[3] BASF Corp, Pasadena, TX USA
[4] Eastman Chem Co, Kingsport, TN 37662 USA
[5] ExxonMobil Biomed Sci Inc, Annandale, NJ USA
[6] Assessment Technol Inc, Keswick, VA USA
来源
HUMAN AND ECOLOGICAL RISK ASSESSMENT | 2011年 / 17卷 / 04期
关键词
phthalate ester; human exposure; biomarker; DUPLICATE DIET SAMPLES; PERSISTENT ORGANIC POLLUTANTS; DEUTERIUM-LABELED DEHP; DI(2-ETHYLHEXYL)PHTHALATE DEHP; HUMAN URINE; DIISONONYL PHTHALATE; GENERAL-POPULATION; INTERNAL EXPOSURE; RISK-ASSESSMENT; UNITED-STATES;
D O I
10.1080/10807039.2011.588157
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
Humans are potentially exposed to phthalate esters (PEs) through ingestion, inhalation, and dermal contact. Studies quantifying exposure to PEs include "biomarker studies" and "indirect studies." Biomarker studies use measurements of PE metabolites in urine to back-calculate exposure to the parent diester, while indirect studies use the concentration of the PE in each medium of exposure and the rate of intake of that medium to quantify intake of the PE. In this review, exposure estimates from biomarker and indirect studies are compiled and compared for seven PEs to determine if there are regional differences and if there is a preferred approach. The indirect and biomarker methods generally agree with each other within an order of magnitude and discrepancies are explained by difficulties in accounting for use of consumer products, uncertainty concerning absorption, regional differences, and temporal changes. No single method is preferred for estimating intake of all PEs; it is suggested that biomarker estimates be used for low molecular weight PEs for which it is difficult to quantify all sources of exposure and either indirect or biomarker methods be used for higher molecular weight PEs. The indirect methods are useful in identifying sources of exposure while the biomarker methods quantify exposure.
引用
收藏
页码:923 / 965
页数:43
相关论文
共 58 条
[1]   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
[2]   Urinary creatinine concentrations in the US population: Implications for urinary biologic monitoring measurements [J].
Barr, DB ;
Wilder, LC ;
Caudill, SP ;
Gonzalez, AJ ;
Needham, LL ;
Pirkle, JL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (02) :192-200
[3]  
BARR DB, 2003, ENV HLTH PERSPECT, V111, P1164
[4]   Estimation of the environmental contamination by phthalic acid esters leaching from household wastes [J].
Bauer, MJ ;
Herrmann, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 1997, 208 (1-2) :49-57
[5]   DEHP metabolites in urine of children and DEHP in house dust [J].
Becker, K ;
Seiwert, M ;
Angerer, J ;
Heger, W ;
Koch, HM ;
Nagorka, R ;
Rosskamp, E ;
Schlüter, C ;
Seifert, B ;
Ullrich, D .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2004, 207 (05) :409-417
[6]   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
[7]  
Brock JW, 2002, B ENVIRON CONTAM TOX, V68, P309, DOI [10.1007/s00128-001-0255-z, 10.1007/s001280255]
[8]   Urinary and amniotic fluid levels of phthalate monoesters in rats after the oral administration of di(2-ethylhexyl) phthalate and di-n-butyl phthalate [J].
Calafat, AM ;
Brock, JW ;
Silva, MJ ;
Gray, LE ;
Reidy, JA ;
Barr, DB ;
Needham, LL .
TOXICOLOGY, 2006, 217 (01) :22-30
[9]   Automated solid phase extraction and quantitative analysis of human milk for 13 phthalate metabolites [J].
Calafat, AM ;
Slakman, AR ;
Silva, MJ ;
Herbert, AR ;
Needham, LL .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 805 (01) :49-56
[10]   Integrating biomonitoring exposure data into the risk assessment process: Phthalates [diethyl phthalate and di(2-ethylhexyl) phthalate] as a case study [J].
Calafat, Antonia M. ;
McKee, Richard H. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2006, 114 (11) :1783-1789