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使用乙酰胆碱酯酶抑制法评估化合物作为有机磷酸酯类经皮渗透屏障的作用。

Evaluation of compounds as barriers to dermal penetration of organophosphates using acetylcholinesterase inhibition.

作者信息

Olson C T, Feder P I, Hobson D W, Kiser R C, Joiner R L

机构信息

Battelle, Columbus, OH 43201-2693.

出版信息

Toxicol Lett. 1991 Mar;55(3):325-34. doi: 10.1016/0378-4274(91)90014-w.

Abstract

An efficient, objective method for evaluating the efficacy of barrier compounds in preventing dermal penetration of organophosphates (OP) in rabbits was developed using time-dependent reduction in erythrocyte (RBC) acetylcholinesterase (AChE) activity as an endpoint. Anesthetized rabbits, with or without a dermal application of a mixture of high- and low-molecular-weight polyethylene glycols (mean molecular weight of 540 daltons; PEG 540), were exposed to different percutaneous doses of 3 highly toxic OP compounds. Dose-response curves were generated for RBC AChE inhibition as a function of percutaneous dose for each OP test material over time. From data generated, a single dose of each OP was selected to challenge PEG-540-protected and unprotected animals to validate the method as a means of differentiating effective from ineffective barriers to skin penetration. Data for a complete evaluation of a PEG 540 test barrier application were obtained within 4 h and anesthesia was maintained for the entire period.

摘要

利用红细胞(RBC)乙酰胆碱酯酶(AChE)活性随时间的降低作为终点指标,开发了一种高效、客观的方法来评估屏障化合物在兔体内预防有机磷酸酯(OP)经皮渗透的效果。将麻醉后的兔子分为两组,一组经皮涂抹高分子量和低分子量聚乙二醇混合物(平均分子量540道尔顿;PEG 540),另一组不涂抹,然后让两组兔子接触不同经皮剂量的3种剧毒OP化合物。随着时间的推移,针对每种OP测试材料,生成红细胞AChE抑制率与经皮剂量的剂量反应曲线。根据生成的数据,选择每种OP的单一剂量来挑战PEG - 540保护组和未保护组动物,以验证该方法作为区分有效和无效皮肤渗透屏障手段的有效性。在4小时内获得了用于完整评估PEG 540测试屏障应用的数据,并且在整个期间维持麻醉状态。

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