Shirai J H, Kissel J C
Delta Toxicology, Seattle, WA 98121, USA.
Sci Total Environ. 1996 Sep 9;187(3):199-210. doi: 10.1016/0048-9697(96)05142-x.
Estimates of the half-lives of PCBs in humans derived from successive body burden measurements are reviewed and found to vary widely whether based on congener-specific or aggregate data. Variability due to differences in physiological processes among individuals and in congener properties is to be expected, but does not appear to be a complete explanation. Very short half-lives (i.e. < 1 year) are unlikely for those congeners most frequently found in human blood because the exposures required to sustain observed body burdens are too large to be easily explained. Very long half-lives ( > 10 years) may be artifacts of confounding by ongoing exposures (a common effect at low body burdens) and are also suspect. The loss of significant quantities of PCBs from the blood of occupationally exposed persons with half-lives of 2-6 years is comparatively well documented (i.e. has been observed in studies with relatively large numbers of subjects and high initial body burdens). Therefore, very long half-lives must be limited to subsets of congeners or of populations if they occur at all. The impact of the use of fixed estimates of half-lives drawn from the tails of the observed range on the evaluation of regulatory standards is shown to be substantial.
对通过连续人体负荷测量得出的多氯联苯在人体内半衰期的估计值进行了审查,发现无论是基于特定同系物数据还是总数据,其差异都很大。由于个体生理过程差异和同系物特性导致的变异性是可以预料的,但这似乎并不是一个完整的解释。对于那些在人体血液中最常见的同系物来说,极短的半衰期(即<1年)不太可能,因为维持观察到的人体负荷所需的接触量太大,难以轻易解释。极长的半衰期(>10年)可能是持续接触造成混淆的假象(在低人体负荷时常见的效应),也令人怀疑。职业暴露人群血液中大量多氯联苯以2至6年的半衰期消失,这方面的记录相对较好(即在有相对大量受试者和高初始人体负荷的研究中观察到)。因此,如果确实存在极长的半衰期,也必须限于同系物子集或人群子集。结果表明,使用从观察范围尾部得出的固定半衰期估计值对监管标准评估的影响很大。