Center for Environmental & Human Toxicology, University of Florida, 2187 Mowry Rd., Gainesville, FL, 32611, USA.
Alloy, LLC, 506 Arapahoe Ave., Boulder, CO, 80302, USA.
Chemosphere. 2019 Jan;214:418-423. doi: 10.1016/j.chemosphere.2018.09.044. Epub 2018 Sep 8.
Bioaccessibilities of PCDD/PCDF congeners contributing to cancer risk were determined in twelve soil samples from the American Creosote Works Superfund site in Florida. Based upon sample locations, congener profiles (i.e., the same dominant congeners), and total (Toxic Equivalent; TEQ) concentrations, each of these samples has PCDD/PCDF contamination reasonably attributable to the site. Bioaccessibility was determined using a 2-phase in vitro extraction method that included both simulated gastric and intestinal conditions of the human GI tract. Measured congener-specific bioaccessibility values ranged from 34.3 to 62.1%. There was no apparent relationship between the extent of chlorination of PCDD/PCDF congeners and their bioaccessibility. TEQ-weighted bioaccessibility values varied among individual soil samples, which is not unexpected based upon the literature. This variability could not be explained by differences in soil pH, composition, or organic carbon content. The average TEQ-weighted bioaccessibility value of 59% for the twelve samples was accepted as representing site-specific bioavailability of PCDD/PCDFs. This value is higher than most dioxin/furan bioaccessibility values reported in the literature and at the upper end of the range of relative oral bioavailability (RBA) values reported for PCDD/PCDFs from in vivo bioavailability studies. This study used a finer fraction of soil particles (<150 microns versus the more typical <250 microns) to better represent soil that is incidentally ingested. This finer fraction would be expected to have a greater surface area available for extraction of PCDD/PCDFs per unit mass, which might account for the greater than expected bioaccessibility.
在佛罗里达州美国防腐油厂超级基金场地的 12 个土壤样本中,测定了对癌症风险有贡献的 PCDD/PCDF 同系物的生物可给性。根据样本位置、同系物分布(即相同的优势同系物)和总(毒性当量;TEQ)浓度,这些样本中的每一个都有 PCDD/PCDF 污染,这与该场地有合理的关系。生物可给性是通过一种 2 相体外提取方法确定的,该方法包括模拟人体胃肠道的胃和肠条件。测定的同系物特异性生物可给性值范围为 34.3%至 62.1%。PCDD/PCDF 同系物的氯化程度与其生物可给性之间没有明显的关系。个体土壤样本之间的 TEQ 加权生物可给性值存在差异,这在文献中是意料之中的。这种可变性不能用土壤 pH 值、组成或有机碳含量的差异来解释。12 个样本的平均 TEQ 加权生物可给性值为 59%,被认为代表了特定场地 PCDD/PCDF 的生物可利用性。这一数值高于文献中报道的大多数二恶英/呋喃生物可给性值,也处于 PCDD/PCDF 体内生物有效性研究中报道的相对口服生物利用率(RBA)值范围的上限。本研究使用了更细的土壤颗粒(<150 微米,而不是更典型的<250 微米),以更好地代表偶然摄入的土壤。由于每单位质量的 PCDD/PCDF 可提取表面积更大,预计这种更细的颗粒的生物可给性会更高。