Suppr超能文献

丙磺舒对头孢孟多血药浓度及尿排泄的影响。

Effect of probenecid on the blood levels and urinary excretion of cefamandole.

作者信息

Griffith R S, Black H R, Brier G L, Wolny J D

出版信息

Antimicrob Agents Chemother. 1977 May;11(5):809-12. doi: 10.1128/AAC.11.5.809.

Abstract

Two oral 0.5-g doses of probenecid given 7 and 1 h before a single 1-g intramuscular dose of cefamandole resulted in higher serum levels of cefamandole than when cefamandole was given alone: 37 versus 20 mug per ml of serum, respectively. Cefamandole was not measurable (<0.3 mug/ml) at 8 h when it was given alone, whereas an average 8-h value of 2.9 mug/ml was obtained after pretreatment with probenecid. By prolonging the duration of these high cefamandole levels, probenecid should permit the treatment of more serious clinical infections, including those due to relatively resistant organisms, or permit a reduction in either the dosage of cefamandole or the frequency of administration.

摘要

在单次肌内注射1g头孢孟多之前7小时和1小时分别口服0.5g丙磺舒,与单独使用头孢孟多相比,可使头孢孟多的血清水平更高:分别为每毫升血清37微克和20微克。单独使用头孢孟多时,8小时时无法测出头孢孟多(<0.3微克/毫升),而在丙磺舒预处理后,8小时的平均数值为2.9微克/毫升。通过延长这些高头孢孟多水平的持续时间,丙磺舒应能用于治疗更严重的临床感染,包括由相对耐药菌引起的感染,或者能减少头孢孟多的剂量或给药频率。

相似文献

4
Kinetics and renal handling of cefonicid.头孢尼西的动力学及肾脏处理过程
Clin Pharmacol Ther. 1981 Nov;30(5):587-93. doi: 10.1038/clpt.1981.208.

引用本文的文献

1
Renal Drug Transporters and Drug Interactions.肾脏药物转运体与药物相互作用
Clin Pharmacokinet. 2017 Aug;56(8):825-892. doi: 10.1007/s40262-017-0506-8.
2
Cephalosporin-probenecid drug interactions.头孢菌素-丙磺舒药物相互作用。
Clin Pharmacokinet. 1993 Apr;24(4):289-300. doi: 10.2165/00003088-199324040-00003.
4
Clinical pharmacokinetics of probenecid.丙磺舒的临床药代动力学。
Clin Pharmacokinet. 1981 Mar-Apr;6(2):135-51. doi: 10.2165/00003088-198106020-00004.

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