School of Resource and Environmental Management, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada.
Toxicology and Environmental Research and Consulting, The Dow Chemical Company, Midland, Michigan 48674, United States.
Environ Sci Technol. 2024 Jun 11;58(23):10252-10261. doi: 10.1021/acs.est.4c00457. Epub 2024 May 29.
With octamethylcyclotetrasiloxane (D4) and decamethylcyclopentasiloxane (D5) being considered for evaluation under the UN Stockholm Convention on Persistent Organic Pollutants, which specifically acknowledges risks of biomagnification of persistent organic pollutants in traditional foods, a study into the mechanism of the biomagnification process of D4 and D5 in Rainbow trout was conducted by combining the absorption-distribution-metabolism-excretion for bioaccumulation (ADME-B) approach to determine intestinal and somatic biotransformation rates and radiochemical analyses to identify metabolite formation. High rates of intestinal biotransformation of D4 and D5 (i.e., 2.1 (0.70 SE) and 0.88 (0.67 SE) day, respectively) and metabolite formation [i.e., 52.0 (17 SD)% of D4 and 56.5% (8.2 SD)% of D5 were metabolized] were observed that caused low dietary uptake efficiencies of D4 and D5 in fish of 15.5 (2.9 SE)% and 21.0 (6.5 SE)% and biomagnification factors of 0.44 (0.08 SE) for D4 and 0.78 (0.24 SE) kg-lipid·kg-lipid for D5. Bioaccumulation profiles indicated little effect of growth dilution on the bioaccumulation of D4 and D5 in fish and were substantially different from those of PCB153. The study highlights the importance of intestinal biotransformation in negating biomagnification of substances in organisms and explains differences between laboratory tests and field observations of bioaccumulation of D4 and D5.
由于八甲基环四硅氧烷(D4)和十甲基环五硅氧烷(D5)被认为需要根据联合国《关于持久性有机污染物的斯德哥尔摩公约》进行评估,该公约特别承认传统食品中持久性有机污染物生物放大的风险,因此进行了一项研究,该研究将吸收-分布-代谢-排泄生物累积(ADME-B)方法与放射性化学分析相结合,以确定 D4 和 D5 在虹鳟鱼中的生物放大过程的机制,从而确定肠道和体组织的生物转化率以及鉴定代谢产物的形成。研究发现 D4 和 D5 的肠道生物转化率很高(即分别为 2.1(0.70 SE)和 0.88(0.67 SE)天),并且代谢产物的形成[即,D4 的 52.0(17 SD)%和 D5 的 56.5%(8.2 SD)%被代谢]导致 D4 和 D5 在鱼中的膳食摄取效率很低,分别为 15.5(2.9 SE)%和 21.0(6.5 SE)%,生物放大因子分别为 0.44(0.08 SE)和 0.78(0.24 SE)kg-脂·kg-脂。生物累积曲线表明,生长稀释对 D4 和 D5 在鱼体内的生物累积几乎没有影响,且与 PCB153 的生物累积曲线有很大不同。该研究强调了肠道生物转化在否定生物体中物质的生物放大方面的重要性,并解释了 D4 和 D5 的实验室测试和现场观察结果之间的差异。