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人血清和尿液中氨环西林的浓度。

Serum and urinary concentrations of cyclacillin in humans.

作者信息

Hertz C G

出版信息

Antimicrob Agents Chemother. 1973 Sep;4(3):361-5. doi: 10.1128/AAC.4.3.361.

Abstract

Cyclacillin is a semisynthetic penicillin produced from the penicillin nucleus (6-aminopenicillanic acid) by acylation with 1-aminohexanecarboxylic acid. The absorption and excretion characteristics of cyclacillin were defined in one completely randomized and three three-way crossover experiments. Mean peak serum cyclacillin levels appeared earlier and were fivefold higher than those obtained with equal doses of ampicillin. High serum cyclacillin concentrations were reached at 0.5 h and by 2 h were lower than ampicillin. Serum ampicillin concentrations peaked at 1.5 h, remaining slightly higher than those for cyclacillin for the next 4.5 h. The mean area for the cyclacillin curve was significantly superior to either of the ampicillin formulations. Mean serum concentrations of cyclacillin exhibited a smooth dose-response, approximately doubling in each instance as the dose was doubled from 250 to 500 and from 500 to 1,000 mg. High concentrations of cyclacillin were also demonstrated in urine. Neither ratio of drug to metabolite in the urine nor the percent of excretion was significantly affected by the dose level. Sixty-seven percent of the drug was excreted unchanged, and 17% was excreted as penicilloic acid, with most of the excretion occurring within 6 h of administration. In subjects given 500 mg of cyclacillin (four times daily) for 6 days, 2% of the drug was excreted as 1-aminocyclohexanecarboxylic acid, and approximately 55% (24 to 91%) was unchanged. Neither formation nor excretion of the former was sex dependent.

摘要

环青霉素是一种半合成青霉素,由青霉素母核(6-氨基青霉烷酸)与1-氨基己酸酰化而成。环青霉素的吸收和排泄特性在一项完全随机试验和三项三向交叉试验中得到了明确。环青霉素的血清平均峰值水平出现得更早,比等剂量氨苄西林的峰值水平高五倍。给药后0.5小时达到高血清环青霉素浓度,到2小时时低于氨苄西林。血清氨苄西林浓度在1.5小时达到峰值,在接下来的4.5小时内仍略高于环青霉素。环青霉素曲线的平均面积显著优于两种氨苄西林制剂中的任何一种。环青霉素的平均血清浓度呈现出平滑的剂量反应,随着剂量从250毫克加倍至500毫克以及从500毫克加倍至1000毫克,每种情况下浓度大约翻倍。尿液中也检测到高浓度的环青霉素。尿液中药物与代谢物的比例以及排泄百分比均未受到剂量水平的显著影响。67%的药物以原形排泄,17%以青霉酸排泄,大部分排泄发生在给药后6小时内。在给予500毫克环青霉素(每日四次)持续6天的受试者中,2%的药物以1-氨基环己烷羧酸形式排泄,约55%(24%至91%)以原形排泄。前者的形成和排泄均与性别无关。

相似文献

1
Serum and urinary concentrations of cyclacillin in humans.人血清和尿液中氨环西林的浓度。
Antimicrob Agents Chemother. 1973 Sep;4(3):361-5. doi: 10.1128/AAC.4.3.361.
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Cyclacillin: a clinical and in vitro profile.环青霉素:临床与体外研究概况
J Infect Dis. 1974 May;129(5):545-51. doi: 10.1093/infdis/129.5.545.
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