Suppr超能文献

阿昔洛韦的临床前毒理学研究:眼科和皮肤试验。

Preclinical toxicology studies with acyclovir: ophthalmic and cutaneous tests.

作者信息

Tucker W E, Johnston R E, Macklin A W, Szot R J, Elion G B, de Miranda P, Szczech G M

出版信息

Fundam Appl Toxicol. 1983 Nov-Dec;3(6):569-72. doi: 10.1016/s0272-0590(83)80106-7.

Abstract

Topical formulations of acyclovir (ACV) were tested in animals to define potential for tissue irritation and systemic toxicity. Acyclovir ointments (5 and 10% concentrations in polyethylene glycol vehicle) produced no sign of dermal irritation or systemic toxicity when applied to shaved abraded and intact skin of guinea pigs for 24 consecutive days. Solutions (0.9% normal saline vehicle) of ACV did not sensitize guinea pigs when 10 sensitizing doses and a challenge dose were injected intradermally. Petrolatum base ophthalmic ointments containing 1 and 3% ACV did not produce significant ocular irritation when applied to the corneas of New Zealand White rabbits 5 times each day for 21 consecutive days. A 6% petrolatum base ointment produced mild conjunctival irritation but no sign of corneal or iridic toxicity. Mean concentrations of 2.53 microM ACV were found in aqueous humor 2 hours after a 1 cm ribbon (21 mg) of 3% ophthalmic ointment was placed in the eyes of rabbits. A single treatment with a topical ointment containing 5% ACV in polyethylene glycol vehicle produced minimal irritation when placed in the eyes of New Zealand White rabbits.

摘要

对阿昔洛韦(ACV)的局部制剂进行了动物试验,以确定其引起组织刺激和全身毒性的可能性。阿昔洛韦软膏(聚乙二醇载体中浓度为5%和10%)连续24天应用于豚鼠剃毛、擦伤和完整的皮肤时,未产生皮肤刺激或全身毒性迹象。当皮内注射10次致敏剂量和一次激发剂量时,阿昔洛韦溶液(0.9%生理盐水载体)未使豚鼠致敏。含1%和3%阿昔洛韦的凡士林基质眼膏连续21天每天5次应用于新西兰白兔角膜时,未产生明显的眼部刺激。一种6%凡士林基质软膏产生轻度结膜刺激,但无角膜或虹膜毒性迹象。将1厘米长的带状(21毫克)3%眼膏置于兔眼2小时后,房水中阿昔洛韦的平均浓度为2.53微摩尔。在聚乙二醇载体中含5%阿昔洛韦的局部软膏单次应用于新西兰白兔眼时,产生的刺激最小。

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