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持续非卧床腹膜透析期间头孢甲肟的药代动力学

Cefmenoxime kinetics during continuous ambulatory peritoneal dialysis.

作者信息

Sica D A, Polk R E, Kerkering T M, Patterson P, Baggett J

出版信息

Eur J Clin Pharmacol. 1986;30(6):713-7. doi: 10.1007/BF00608221.

DOI:10.1007/BF00608221
PMID:3464435
Abstract

The kinetics of the aminothiazolyliminomethoxy cephalosporin, cefmenoxime, were determined after a 30 min intravenous infusion of 15 mg/kg body weight in 6 adult subjects undergoing continuous ambulatory peritoneal dialysis. Concentrations of cefmenoxime in serum, urine and dialysate were determined by high-pressure liquid chromatography. The mean peak serum concentration was 92.8 +/- 11.6 micrograms/ml and the harmonic mean for the elimination half-life was 5.46 h. The volume of distribution at steady-state was 14.60 +/- 3.01 l/kg. Total body clearance of the drug was 31 +/- 7.7 ml/min with 8 +/- 5% and 5.75 +/- 2.72% of the administered dose being eliminated by renal and peritoneal clearance, respectively. Peritoneal clearance for all exchanges (n = 24) was 1.93 +/- 68 ml/min. These data suggest that peritoneal losses of this drug are minimal and doses conventionally employed in advanced renal failure can be utilized in the management of systemic infections.

摘要

在6名接受持续性非卧床腹膜透析的成年受试者中,静脉输注15mg/kg体重的氨噻唑基亚氨基甲氧基头孢菌素头孢甲肟30分钟后,测定其药代动力学。采用高压液相色谱法测定血清、尿液和透析液中头孢甲肟的浓度。血清平均峰浓度为92.8±11.6μg/ml,消除半衰期的调和平均值为5.46小时。稳态分布容积为14.60±3.01l/kg。该药的总体清除率为31±7.7ml/min,给药剂量分别有8±5%和5.75±2.72%经肾脏清除和腹膜清除。所有交换(n=24)的腹膜清除率为1.93±68ml/min。这些数据表明,该药的腹膜清除量极少,晚期肾衰竭时常规使用的剂量可用于全身性感染的治疗。

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本文引用的文献

1
Unidirectional absorption of gentamicin from the peritoneum during continuous ambulatory peritoneal dialysis.持续性非卧床腹膜透析期间庆大霉素从腹膜的单向吸收
Clin Pharmacol Ther. 1982 Jul;32(1):113-21. doi: 10.1038/clpt.1982.134.
2
Tobramycin kinetics during continuous ambulatory peritoneal dialysis.持续非卧床腹膜透析期间妥布霉素的动力学
Clin Pharmacol Ther. 1983 Jul;34(1):110-6. doi: 10.1038/clpt.1983.138.
3
Cefazolin and cephalexin kinetics in continuous ambulatory peritoneal dialysis.
Clin Pharmacol Ther. 1983 Jan;33(1):66-72. doi: 10.1038/clpt.1983.9.
4
Microbiologic aspects of chronic ambulatory peritoneal dialysis.慢性非卧床腹膜透析的微生物学方面
Kidney Int. 1983 Jan;23(1):83-92. doi: 10.1038/ki.1983.15.
5
Effect of protein binding on cefmenoxime steady-state kinetics in critical patients.
Clin Pharmacol Ther. 1984 Jan;35(1):64-73. doi: 10.1038/clpt.1984.10.
6
Effect of probenecid on the pharmacokinetics of cefmenoxime.丙磺舒对头孢甲肟药代动力学的影响。
Antimicrob Agents Chemother. 1983 Jun;23(6):803-7. doi: 10.1128/AAC.23.6.803.
7
High-performance liquid chromatographic determination of cefmenoxime (AB-50912) in human plasma and urine.高效液相色谱法测定人血浆和尿液中的头孢甲肟(AB - 50912)
J Chromatogr. 1983 Apr 8;273(2):458-63. doi: 10.1016/s0378-4347(00)80971-8.
8
Intramuscular and intravenous pharmacokinetics of cefmenoxime, a new broad-spectrum cephalosporin, in healthy subjects.新型广谱头孢菌素头孢甲肟在健康受试者中的肌内和静脉药代动力学
Antimicrob Agents Chemother. 1982 Jan;21(1):141-5. doi: 10.1128/AAC.21.1.141.
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Antimicrob Agents Chemother. 1984 Dec;26(6):845-9. doi: 10.1128/AAC.26.6.845.
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Am J Med. 1984 Dec 21;77(6A):1-3. doi: 10.1016/s0002-9343(84)80063-7.