三甲基丙烷三丙烯酸酯(技术等级)(CASRN 15625-89-5)对F344/N大鼠和B6C3F1/N小鼠的毒理学和致癌作用研究(皮肤研究)。

Q4 Medicine National Toxicology Program technical report series Pub Date : 2012-12-01
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引用次数: 0

摘要

背景:三甲基丙烷三丙烯酸酯(TMPTA)被广泛用作涂料、树脂、光敏材料和高吸水性婴儿尿布的成分。我们研究了TMPTA对雄性和雌性大鼠和小鼠的影响,以确定潜在的毒性或癌症相关危害。方法:将含丙酮的TMPTA溶液应用于雌雄大鼠和小鼠背部。每组50只雄性和雌性大鼠和小鼠,每公斤体重接受0.3、1或3毫克TMPTA,每周5天,持续两年。单独注射丙酮的动物组为对照组。在研究结束时,对每只动物的40多个部位的组织进行了检查。结果:各暴露组动物的存活率和体重与对照组相似。在所有接受1 mg/kg或更多剂量的动物组中,在化学物质施用部位的皮肤中观察到表皮增生。在接受TMPTA的大鼠中,涂抹部位角化过度也有所增加,并且在接受TMPTA的雄性和雌性小鼠的皮肤中也可见慢性炎症。少数雄性大鼠暴露于TMPTA中可见恶性间皮瘤。在一些暴露于TMPTA的雌性小鼠中观察到两种不同的罕见形式的肝癌(肝母细胞瘤和肝胆管癌),并且在一些暴露于TMPTA的雌性小鼠中也发生了子宫肿瘤(间质息肉或间质肉瘤)。结论:我们得出结论,暴露于TMPTA导致雌性小鼠罕见的肝癌和子宫肿瘤,并可能与雄性大鼠恶性间皮瘤的发生有关。在雌性大鼠或雄性小鼠中,没有癌症的发生与接触TMPTA有关。暴露于高浓度TMPTA的所有动物组均出现涂药部位的皮肤病变,包括大鼠和小鼠的增生、大鼠角化过度和小鼠的炎症。
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Toxicology and carcinogenesis studies of trimethylolpropane triacrylate (technical grade) (CASRN 15625-89-5) in F344/N rats and B6C3F1/N mice (dermal studies).

Background: Trimethylolpropane triacrylate (TMPTA) is used as an ingredient in a wide variety of coatings, resins, photosensitive materials, and superabsorbent baby diapers. We studied the effects of TMPTA on male and female rats and mice to identify potential toxic or cancer-related hazards.

Methods: We applied solutions containing TMPTA in acetone on the backs of male and female rats and mice. Groups of 50 male and female rats and mice received 0.3, 1, or 3 milligrams of TMPTA per kilogram of body weight five days per week for two years. Groups of animals receiving acetone alone served as the control groups. At the end of the study, tissues from more than 40 sites were examined for every animal.

Results: Survival and body weights of all groups of exposed animals were similar to the control groups. Epidermal hyperplasia was observed in the skin at the site where the chemical was applied in all groups of animals receiving 1 mg/kg or more. Hyperkeratosis at the site of application was also increased in rats receiving TMPTA, and chronic inflammation was also seen in the skin of male and female mice receiving TMPTA. Malignant mesotheliomas were seen in a few male rats exposed to TMPTA. Two different rare forms of liver cancer (hepatoblastoma and hepatocholangiocarcinoma) were observed in some of the female mice exposed to TMPTA, and tumors of the uterus (stromal polyp or stromal sarcoma) also occurred in some exposed female mice.

Conclusions: We conclude that exposure to TMPTA caused rare cancers of the liver and tumors of the uterus in female mice and may have been related to the occurrence of malignant mesothelioma in male rats. No occurrences of cancer were associated with exposure to TMPTA in female rats or male mice. Skin lesions at the site of application, including hyperplasia in rats and mice, hyperkeratosis in rats, and inflammation in mice occurred in all animal groups exposed to higher concentrations of TMPTA.

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