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安吡昔康,一种抗炎药,是吡罗昔康的前体药物。

Ampiroxicam, an anti-inflammatory agent which is a prodrug of piroxicam.

作者信息

Carty T J, Marfat A, Moore P F, Falkner F C, Twomey T M, Weissman A

机构信息

Department of Immunology and Infectious Disease, Pfizer Inc, Groton, CT 06340.

出版信息

Agents Actions. 1993 Jul;39(3-4):157-65. doi: 10.1007/BF01998969.

Abstract

Ampiroxicam is a nonacidic ether carbonate prodrug of piroxicam. Our results demonstrate that, in contrast to piroxicam, ampiroxicam does not possess detectable prostaglandin synthesis inhibitory activity in vitro. Ampiroxicam, however, has similar in vivo potency to piroxicam in suppressing paw swelling in rat adjuvant arthritis. In an acute model of paw inflammation in rats, ampiroxicam is less potent than piroxicam itself: the ED50's of ampiroxicam are 9- and 3.5-fold higher than those of piroxicam following a single or multiple (5) daily oral doses, respectively. Using the phenylbenzoquinone stretching test as a method of evaluating acute analgetic activity, the ED50 for ampiroxicam is about 3-fold higher than that of piroxicam. These tests of activity share the property of being partially prostaglandin-dependent. Ampiroxicam itself is not observed in plasma after oral dosing to man, nor in the rat, dog, and monkey as reported here. Bioavailability studies show that conversion to piroxicam is about 100%, 90%, 70%, and 50% in these four species, respectively. These results indicate that ampiroxicam's anti-inflammatory activity is produced in vivo by conversion to piroxicam and support its credentials as an efficacious prodrug of piroxicam.

摘要

安吡昔康是吡罗昔康的一种非酸性醚碳酸盐前体药物。我们的研究结果表明,与吡罗昔康不同,安吡昔康在体外不具有可检测到的前列腺素合成抑制活性。然而,在抑制大鼠佐剂性关节炎爪肿胀方面,安吡昔康在体内的效力与吡罗昔康相似。在大鼠爪部炎症的急性模型中,安吡昔康的效力低于吡罗昔康本身:单次或多次(5次)每日口服给药后,安吡昔康的半数有效剂量(ED50)分别比吡罗昔康高9倍和3.5倍。使用苯醌拉伸试验作为评估急性镇痛活性的方法,安吡昔康的ED50比吡罗昔康高约3倍。这些活性测试都具有部分依赖前列腺素的特性。口服给药后,在人体血浆中未检测到安吡昔康本身,在此处报道的大鼠、狗和猴中也未检测到。生物利用度研究表明,在这四个物种中,转化为吡罗昔康的比例分别约为100%、90%、70%和50%。这些结果表明,安吡昔康的抗炎活性是通过在体内转化为吡罗昔康产生的,并支持其作为吡罗昔康有效前体药物的资质。

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