Norris J M, Kociba R J, Schwetz B A, Rose J Q, Humiston C G, Jewett G L, Gehring P J, Mailhes J B
Environ Health Perspect. 1975 Jun;11:153-61. doi: 10.1289/ehp.7511153.
Decabromodiphenyl oxide (DBDPO) and octabromobiphenyl (OBBP) perform well as fire-retardant additives for thermoplastics. Both compounds have low acute oral toxicity and low skin absorption toxicity. They are neither primary skin irritants or skin sensitizers and are only mildly irritating to the eyes. A 30-day dietary feeding study in rats established 8 mg DBDPO/kg-day as an unequivocal no-effect level and 80 mg/kg-day as a marginal effect level. A no-effect level was not established for OBBP in a comparative study. A 2-yr rat study providing 0.1 mg DBDPO/kg-day in the diet revealed the bromine concentration reached a plateau in the liver within 30 days, while the concentration in adipose tissue slowly increased. A comparable OBBP study revealed bromine concentration in the liver and adipose tissue increased steadily and rapidly with no attainment of a plateau during 180 days of the study. Neither compound produced an accumulation of bromine in other tissues. After administration of 14C DBDPO, all 14C activity was eliminated via the feces within 2 days. After administration of 14C OBBP, 62% was eliminated with a half-life of less than 24 hr; the half-life for the remainder was greater than 16 days. In a teratology study, 10, 100, or 1000 mg DBDPO/kg-day had no effect in rats. Reproductive capacity of rats was not effected at 3, 30, or 100 mg DBDPO/kg-day. No effects were observed on cytogenetic examination of bone marrow cells of parents and weanlings from the reproduction study.
十溴二苯醚(DBDPO)和八溴联苯(OBBP)作为热塑性塑料的阻燃添加剂表现良好。这两种化合物的急性经口毒性和皮肤吸收毒性都很低。它们既不是原发性皮肤刺激物,也不是皮肤致敏剂,对眼睛只有轻微刺激。在大鼠中进行的一项为期30天的饮食喂养研究确定,8毫克DBDPO/千克·天为明确的无效应水平,80毫克/千克·天为边缘效应水平。在一项比较研究中,未确定OBBP的无效应水平。一项为期两年的大鼠研究显示,在饮食中提供0.1毫克DBDPO/千克·天,肝脏中的溴浓度在30天内达到稳定状态,而脂肪组织中的浓度则缓慢增加。一项类似的OBBP研究显示,在研究的180天内,肝脏和脂肪组织中的溴浓度稳步快速增加,未达到稳定状态。这两种化合物在其他组织中均未产生溴的蓄积。给予14C-DBDPO后,所有14C活性在2天内通过粪便排出。给予14C-OBBP后,62%在半衰期小于24小时内排出;其余部分的半衰期大于16天。在一项致畸学研究中,10、100或1000毫克DBDPO/千克·天对大鼠没有影响。在3、30或100毫克DBDPO/千克·天的剂量下,大鼠的生殖能力未受影响。在生殖研究中,对亲代和断奶幼仔的骨髓细胞进行细胞遗传学检查未观察到任何影响。