Suppr超能文献

甲基丙烯酸二环戊烯氧基乙酯对兔和豚鼠的急性毒性、亚慢性皮肤毒性及迟发性接触致敏性评估

Acute toxicity, subchronic dermal toxicity, and delayed contact sensitization evaluations of dicyclopentenyloxyethyl methacrylate in rabbits and guinea pigs.

作者信息

Chan P K, Baldwin R C, Fedorowski A, O'Hara G P, Hayes A W, Smith J M, Barthel C H

出版信息

J Toxicol Environ Health. 1985;16(1):39-54. doi: 10.1080/15287398509530717.

Abstract

The subchronic dermal toxicity of dicyclopentenyloxethyl methacrylate (DPOMA) was evaluated in young adult New Zealand White rabbits, and its potential to produce delayed contact sensitization was evaluated in Harley guinea pigs by a modified Buehler's closed patch technique. In addition, studies were conducted to evaluate the acute systemic toxicity of DPOMA in rats (oral) and rabbits (dermal), and its eye and skin irritancy in rabbits. In the subchronic dermal toxicity study, 4 groups of rabbits were treated percutaneously with DPOMA at 0 (acetone), 10, 107, and 1067 (undiluted) mg/kg X day in a volume of 1 ml/kg, over a 4-wk period. The application sites were unoccluded. No deaths occurred, and no signs of systemic toxicity were observed. No treatment-related effects were seen on body weights, hematology, clinical chemistry, urinalysis, organ weights, or histopathology (except the treated skin). The only treatment-related effect was slight to moderate skin irritation in the mid- and high-dose groups. The severity of skin irritaton was dependent on the number of applications and the concentration of DPOMA. Maximal skin irritation occurred after 1 wk. No skin irritation was seen in the control and low-dose group. In the DCS study, guinea pigs received 6 induction doses of 0.5 ml 100% DPOMA and were challenged with 0.5 ml of 50% (w/v) DPOMA in acetone 2 wk after the last induction treatment. No erythema or edema was observed in any of the challenged guinea pigs in either the treated and control groups. These acute toxicity studies indicate that DPOMA is practically nontoxic by a single exposure via both oral and dermal routes (the oral LD50 in rat and dermal LD50 in rabbits were greater than 5.0 g/kg body weight), slightly irritating to the skin, and inconsequentially irritating to the eyes. The no-observed-effect level (NOEL) for systemic toxicity of DPOMA applied repeatedly to rabbits skin is at least 1067 mg/kg X d. DPOMA is not a strong or moderate skin sensitizer in guinea pigs.

摘要

在成年新西兰白兔中评估了甲基丙烯酸二环戊烯氧基乙酯(DPOMA)的亚慢性皮肤毒性,并通过改良的布勒氏封闭贴片技术在哈雷豚鼠中评估了其产生迟发性接触性致敏的可能性。此外,还进行了研究以评估DPOMA对大鼠(经口)和兔子(经皮)的急性全身毒性,以及对兔子的眼和皮肤刺激性。在亚慢性皮肤毒性研究中,4组兔子在4周内以1 ml/kg的体积,按0(丙酮)、10、107和1067(未稀释)mg/kg·天的剂量经皮给予DPOMA。涂抹部位未封闭。未发生死亡,也未观察到全身毒性迹象。在体重、血液学、临床化学、尿液分析、器官重量或组织病理学(处理过的皮肤除外)方面未观察到与处理相关的影响。唯一与处理相关的影响是中、高剂量组出现轻度至中度皮肤刺激。皮肤刺激的严重程度取决于涂抹次数和DPOMA的浓度。最大皮肤刺激在1周后出现。对照组和低剂量组未观察到皮肤刺激。在迟发性接触性致敏研究中,豚鼠接受6次0.5 ml 100% DPOMA的诱导剂量,并在最后一次诱导处理后2周用0.5 ml丙酮中50%(w/v)的DPOMA进行激发。在处理组和对照组的任何激发豚鼠中均未观察到红斑或水肿。这些急性毒性研究表明,DPOMA通过经口和经皮单次暴露实际上无毒(大鼠经口LD50和兔子经皮LD50均大于5.0 g/kg体重),对皮肤有轻微刺激性,对眼睛刺激性不大。反复涂抹于兔子皮肤的DPOMA全身毒性的未观察到影响水平(NOEL)至少为1067 mg/kg·天。DPOMA在豚鼠中不是强或中度皮肤致敏剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验