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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。

相似文献

1
In vivo phototoxicity of non-steroidal anti-inflammatory drugs evaluated by the mouse tail technique.通过小鼠尾巴技术评估非甾体抗炎药的体内光毒性。
Photodermatol. 1985 Dec;2(6):377-82.
2
Phototoxicity of non-steroidal anti-inflammatory drugs demonstrated in vitro by a photo-basophil-histamine-release test.通过光嗜碱性粒细胞组胺释放试验在体外证实的非甾体抗炎药的光毒性。
Photodermatol. 1987 Apr;4(2):73-8.
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Propionic acid-derived non-steroidal antiinflammatory drugs are phototoxic in vitro.丙酸衍生的非甾体抗炎药在体外具有光毒性。
Photodermatol. 1985 Feb;2(1):3-9.
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[Photosensitizing properties of nonsteroidal antirheumatic drugs in the photopatch test].[非甾体类抗风湿药物在光斑贴试验中的光敏特性]
Hautarzt. 1987 Jan;38(1):18-25.
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Acta Derm Venereol. 1977;57(4):325-9.
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Phototoxic properties of quinine and quinidine: two quinoline methanol isomers.奎宁和奎尼丁的光毒性特性:两种喹啉甲醇异构体。
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[Photosensitization by Benoxaprofen (author's transl)].贝诺洛芬引起的光敏反应(作者译)
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引用本文的文献

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Enhanced Removal and Toxicity Declineof Diclofenac by Combining UVA Treatmentand Adsorption of Photoproductsto Polyvinylidene Difluoride.通过结合UVA处理和光产物对聚偏二氟乙烯的吸附增强双氯芬酸的去除及毒性降低
Polymers (Basel). 2020 Oct 13;12(10):2340. doi: 10.3390/polym12102340.
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Drug-induced cutaneous photosensitivity: incidence, mechanism, prevention and management.药物性皮肤光敏反应:发病率、机制、预防及处理
Drug Saf. 2002;25(5):345-72. doi: 10.2165/00002018-200225050-00004.
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Photosensitivity to ketoprofen: mechanisms and pharmacoepidemiological data.
酮洛芬的光敏性:作用机制与药物流行病学数据
Drug Saf. 2000 May;22(5):339-49. doi: 10.2165/00002018-200022050-00002.
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Tiaprofenic acid. A reappraisal of its pharmacological properties and use in the management of rheumatic diseases.噻洛芬酸。对其药理特性及在风湿性疾病治疗中的应用的重新评估。
Drugs. 1995 Dec;50(6):1050-75. doi: 10.2165/00003495-199550060-00010.