Olsen Geary W, Chang Shu-Ching, Noker Patricia E, Gorman Gregory S, Ehresman David J, Lieder Paul H, Butenhoff John L
Medical Department, 3M Company, St. Paul, MN 55144-1000, USA.
Toxicology. 2009 Feb 4;256(1-2):65-74. doi: 10.1016/j.tox.2008.11.008. Epub 2008 Nov 19.
Materials derived from perfluorobutanesulfonyl fluoride (PBSF, C(4)F(9)SO(2)F) have been introduced as replacements for eight-carbon homolog products that were manufactured from perfluorooctanesulfonyl fluoride (POSF, C(8)F(17)SO(2)F). Perfluorobutanesulfonate (PFBS, C(4)F(9)SO(3)(-)) is a surfactant and potential degradation product of PBSF-derived materials. The purpose of this series of studies was to evaluate the pharmacokinetics of PFBS in rats, monkeys, and humans, thereby providing critical information for human health risk assessment. Studies included: (1) intravenous (i.v.) elimination studies in rats and monkeys; (2) oral uptake and elimination studies in rats; and (3) human serum PFBS elimination in a group of workers with occupational exposure to potassium PFBS (K(+)PFBS). PFBS concentrations were determined in serum (all species), liver (rats), urine (all species), and feces (rats). In rats, the mean terminal serum PFBS elimination half-lives, after i.v. administration of 30mg/kg PFBS, were: males 4.51+/-2.22h (standard error) and females 3.96+/-0.21h. In monkeys, the mean terminal serum PFBS elimination half-lives, after i.v. administration of 10mg/kg PFBS, were: males 95.2+/-27.1h and females 83.2+/-41.9h. Although terminal serum half-lives in male and female rats were similar, without statistical significance, clearance (CL) was significantly greater in female rats (469+/-40mL/h) than male rats (119+/-34mL/h) with the area under the curve (AUC) significantly larger in male rats (294+/-77microg.h/mL) than female rats (65+/-5microg.h/mL). These differences were not observed in male and female monkeys. Volume of distribution estimates suggested distribution was primarily extracellular in both rats and monkeys, regardless of sex, and urine appeared to be a major route of elimination. Among 6 human subjects (5 male, 1 female) followed up to 180 days, the geometric mean serum elimination half-life for PFBS was 25.8 days (95% confidence interval 16.6-40.2). Urine was observed to be a pathway of elimination in the human. Although species-specific differences exist, these findings demonstrate that PFBS is eliminated at a greater rate from human serum than the higher chain homologs of perfluorooctanesulfonate (PFOS) and perfluorohexanesulfonate (PFHxS). Thus, compared to PFOS and PFHxS, PFBS has a much lower potential for accumulation in human serum after repeated occupational, non-occupational (e.g., consumer), or environmental exposures.
源自全氟丁烷磺酰氟(PBSF,C(4)F(9)SO(2)F)的材料已被引入,以替代由全氟辛烷磺酰氟(POSF,C(8)F(17)SO(2)F)制造的八碳同系物产品。全氟丁烷磺酸盐(PFBS,C(4)F(9)SO(3)(-))是一种表面活性剂,也是源自PBSF材料的潜在降解产物。这一系列研究的目的是评估PFBS在大鼠、猴子和人类中的药代动力学,从而为人类健康风险评估提供关键信息。研究包括:(1)大鼠和猴子的静脉注射消除研究;(2)大鼠的口服摄取和消除研究;(3)一组职业接触全氟丁酸钾(K(+)PFBS)的工人的人血清PFBS消除研究。在血清(所有物种)、肝脏(大鼠)、尿液(所有物种)和粪便(大鼠)中测定了PFBS浓度。在大鼠中,静脉注射30mg/kg PFBS后,血清PFBS的平均终末消除半衰期为:雄性4.51±2.22小时(标准误差),雌性3.96±0.21小时。在猴子中,静脉注射10mg/kg PFBS后,血清PFBS的平均终末消除半衰期为:雄性95.2±27.1小时,雌性83.2±41.9小时。虽然雄性和雌性大鼠的终末血清半衰期相似,无统计学意义,但雌性大鼠的清除率(CL)(469±40mL/h)显著高于雄性大鼠(119±34mL/h),而雄性大鼠的曲线下面积(AUC)(294±77μg·h/mL)显著大于雌性大鼠(65±5μg·h/mL)。在雄性和雌性猴子中未观察到这些差异。分布容积估计表明,无论性别,大鼠和猴子体内的分布主要在细胞外,尿液似乎是主要的消除途径。在随访至180天的6名人类受试者(5名男性,1名女性)中,PFBS的几何平均血清消除半衰期为25.8天(95%置信区间16.6 - 40.2)。观察到尿液是人类的一种消除途径。尽管存在物种特异性差异,但这些发现表明,与全氟辛烷磺酸(PFOS)和全氟己烷磺酸(PFHxS)的高链同系物相比,PFBS从人血清中的消除速度更快。因此,与PFOS和PFHxS相比,在反复职业、非职业(如消费者)或环境暴露后,PFBS在人血清中积累的可能性要低得多。