Suppr超能文献

[阿扎丙宗抗风湿治疗期间洋地黄毒苷的动力学(作者译)]

[Kinetics of digitoxin during antirheumatic therapy with azapropazone (author's transl)].

作者信息

Faust-Tinnefeldt G, Gilfrich H J

出版信息

Arzneimittelforschung. 1977;27(10):2009-11.

PMID:579114
Abstract

The effect of chronic therapy with 5-dimethylamino-9-methylamino-9-methyl-2-propyl-1H-pyrazolo[1,2-a] [1,2,4] benzotriazine-1,3-(2H)-dione-dihydrate (azapropazone-dihydrate; Prolixan 300) on the elimination of a single i.v. dose of digitoxin was studied in 8 patients with rheumatoid arthritis and osteoarthritis using a crossover design. 0.5 mg digitoxin were injected i.v. alone and together with a chronic oral therapy of azapropazone starting 3 weeks before digitoxin was given. Digitoxin plasma levels were determined by radioimmunoassay over a period of 19 days. The half-life for plasma digitoxin was 6.4 +/- 0.5 days after digitoxin alone and 7.0 +/- 0.6 days during azapropazone treatment. In two patients the half-life of digitoxin was increased by about one-third during azapropazone therapy. The areas under the plasma digitoxin curve were 2592 +/- 262 ng/ml X h and 2615 +/- 273 ng/ml X h, respectively. None of the differences were statistically significant. It was concluded that there was no clinically significant interaction between azapropazone and a single dose of digitoxin.

摘要

采用交叉设计,在8例类风湿性关节炎和骨关节炎患者中研究了5-二甲基氨基-9-甲氨基-9-甲基-2-丙基-1H-吡唑并[1,2-a][1,2,4]苯并三嗪-1,3-(2H)-二酮二水合物(阿扎丙宗二水合物;Prolixan 300)长期治疗对单次静脉注射洋地黄毒苷消除的影响。在静脉注射0.5 mg洋地黄毒苷时,分别单独给药以及在给予洋地黄毒苷前3周开始联合阿扎丙宗进行长期口服治疗。通过放射免疫分析法在19天内测定洋地黄毒苷的血浆水平。单独使用洋地黄毒苷时,血浆洋地黄毒苷的半衰期为6.4±0.5天,在阿扎丙宗治疗期间为7.0±0.6天。在两名患者中,阿扎丙宗治疗期间洋地黄毒苷的半衰期增加了约三分之一。血浆洋地黄毒苷曲线下面积分别为2592±262 ng/ml·h和2615±273 ng/ml·h。这些差异均无统计学意义。得出的结论是,阿扎丙宗与单次剂量的洋地黄毒苷之间不存在具有临床意义的相互作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验