Comparison of the toxicokinetics between perfluorocarboxylic acids with different carbon chain length

被引:199
作者
Ohmori, K
Kudo, N
Katayama, K
Kawashima, Y
机构
[1] Josai Univ, Fac Pharmaceut Sci, Sakado, Saitama 3500295, Japan
[2] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Toyama 9300194, Japan
关键词
perfluorocarboxylic acids; toxicokinetics; renal clearance;
D O I
10.1016/S0300-483X(02)00573-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Toxicokinetics was compared between perfluoroheptanoic acid (PFHA), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA) and perfluorodecanoic acid (PFDA) in male and female rats. Half lives (t(1/2)) in male and female rats were calculated to be 0.10 and 0.05 days, respectively, for PFHA, 5.63 and 0.08 days for PFOA, 29.5 and 2.44 days for PFNA and 39.9 and 58.6 days for PFDA. Total clearance (CLtot) of PFHA was higher than those of other perfluorocarboxylic acids (PFCAs) in both male and female rats. By contrast, CLtot of PFDA was extremely low in both sexes. PFCAs having shorter carbon chain length showed higher CLtot. There was a significant sex-related difference in CLtot of PFOA and PFNA. Distribution volumes in steady state (V-ss) were not much different between PFCAs and between sexes. To estimate the role of urinary excretion in plasma clearance of PFCA, renal clearance (CLR) was determined for PFCAs. CLR of PFCAs were in the order PFHA > PFOA > PFNA similar or equal to PFDA and PFHA similar or equal to PFOA > PDNA > PFDA in male and female rats, respectively. There was a close relationship between CLtot and CLR (r(2) = 0.981). Plasma protein binding, estimated in vitro, was over 98% for all PFCAs tested. The results indicate that CLR is responsible for the difference in CLtot between PFCAs having different carbon chain length and between sexes. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:135 / 140
页数:6
相关论文
共 13 条
[1]  
GUETHNER RA, 1962, IND ENG CHEM PROD RD, V1, P165
[2]   DISPOSITION OF PERFLUORODECANOIC ACID IN MALE AND FEMALE RATS [J].
HEUVEL, JPV ;
KUSLIKIS, BI ;
VANRAFELGHEM, MJ ;
PETERSON, RE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 107 (03) :450-459
[3]   Sex hormone-regulated renal transport of perfluorooctanoic acid [J].
Kudo, N ;
Katakura, M ;
Sato, Y ;
Kawashima, Y .
CHEMICO-BIOLOGICAL INTERACTIONS, 2002, 139 (03) :301-316
[4]   Comparison of the elimination between perfluorinated fatty acids with different carbon chain length in rats [J].
Kudo, N ;
Suzuki, E ;
Katakura, M ;
Ohmori, K ;
Noshiro, R ;
Kawashima, Y .
CHEMICO-BIOLOGICAL INTERACTIONS, 2001, 134 (02) :203-216
[5]   LACK OF EVIDENCE FOR PERFLUORODECANOYL- OR PERFLUOROOCTANOYL-COENZYME-A FORMATION IN MALE AND FEMALE RATS [J].
KUSLIKIS, BI ;
VANDENHEUVEL, JP ;
PETERSON, RE .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1992, 7 (01) :25-29
[6]   Determination of perfluorinated carboxylic acids in biological samples by high-performance liquid chromatography [J].
Ohya, T ;
Kudo, N ;
Suzuki, E ;
Kawashima, Y .
JOURNAL OF CHROMATOGRAPHY B, 1998, 720 (1-2) :1-7
[7]   THE ACUTE TOXICITY OF PERFLUOROOCTANOIC AND PERFLUORODECANOIC ACIDS IN MALE-RATS AND EFFECTS ON TISSUE FATTY-ACIDS [J].
OLSON, CT ;
ANDERSEN, ME .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1983, 70 (03) :362-372
[8]  
OPHAUG RH, 1980, P SOC EXP BIOL MED, V163, P19
[9]   ESTIMATION OF RENAL SECRETORY FUNCTION FOR ORGANIC CATIONS BY ENDOGENOUS N1-METHYLNICOTINAMIDE IN RATS WITH EXPERIMENTAL RENAL-FAILURE [J].
SHIM, CK ;
SAWADA, Y ;
IGA, T ;
HANANO, M .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1984, 12 (01) :23-42
[10]   HEALTH-STATUS OF PLANT WORKERS EXPOSED TO FLUOROCHEMICALS - A PRELIMINARY-REPORT [J].
UBEL, FA ;
SORENSON, SD ;
ROACH, DE .
AMERICAN INDUSTRIAL HYGIENE ASSOCIATION JOURNAL, 1980, 41 (08) :584-589