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通过小鼠尾巴技术评估非甾体抗炎药的体内光毒性。

In vivo phototoxicity of non-steroidal anti-inflammatory drugs evaluated by the mouse tail technique.

作者信息

Ljunggren B, Lundberg K

出版信息

Photodermatol. 1985 Dec;2(6):377-82.

PMID:4094928
Abstract

Skin photosensitivity is a side-effect reported for several non-steroidal anti-inflammatory drugs (NSAID). In vitro studies have revealed phototoxic properties in a majority of these compounds with a preponderance for derivatives of propionic acid. Fourteen NSAIDs, the majority commercial preparations in clinical use, have been assayed by the mouse tail technique for in vivo phototoxicity evaluation. Intraperitoneal single doses in the range 12.5-200 mg/kg were given in combination with UVA irradiation for 5 h (total dose 54 J/cm2). The phototoxic reaction was measured 24 h later as the wet weight increase of tail tissue over non-irradiated, drug-treated controls. Four out of 9 propionic acid derivatives were phototoxic: tiaprofenic acid, carprofen, benoxaprofen and naproxen. Among NSAID compounds of other chemical structure only diclofenac and diflunisal were weakly photoactive. The propionic acid derivatives fenoprofen, flurbiprofen, ibuprofen, indoprofen and ketoprofen were negative, as were azapropazone, piroxicam and sulindac among the unrelated compounds. Phototoxicity is one important aspect of NSAID photosensitization. It is advisable to perform predictive studies including in vivo models, such as the mouse tail technique, before new NSAIDs are introduced on the market.

摘要

皮肤光敏性是几种非甾体抗炎药(NSAID)报告的一种副作用。体外研究表明,这些化合物中的大多数具有光毒性,其中丙酸衍生物占多数。采用小鼠尾巴技术对14种NSAID进行了体内光毒性评估,这些药物大多是临床使用的商业制剂。腹腔注射单剂量为12.5 - 200mg/kg,并结合UVA照射5小时(总剂量54J/cm²)。24小时后测量光毒性反应,以尾巴组织湿重相对于未照射的药物处理对照的增加量来衡量。9种丙酸衍生物中有4种具有光毒性:噻洛芬酸、卡洛芬、苯恶洛芬和萘普生。在其他化学结构的NSAID化合物中,只有双氯芬酸和二氟尼柳具有微弱的光活性。丙酸衍生物非诺洛芬、氟比洛芬、布洛芬、吲哚洛芬和酮洛芬呈阴性,在不相关化合物中阿扎丙宗、吡罗昔康和舒林酸也呈阴性。光毒性是NSAID光敏化的一个重要方面。在新的NSAID上市之前,建议进行包括体内模型(如小鼠尾巴技术)在内的预测性研究。

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