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Clinical pharmacology of a new ureidopenicillin: Bay K 49999.

作者信息

Lode H, Tomas W, Koeppe P, Wagner J

出版信息

Chemotherapy. 1980;26(2):81-90. doi: 10.1159/000237887.

DOI:10.1159/000237887
PMID:7363710
Abstract

A new semisynthetic ureidopenicillin (Bay K 4999) demonstrates favorably in vitro antibacterial efficacy against human-pathogenic gram-negative rods in comparison to mezlocillin and azlocillin. A comparative paramcokinetic study was done with 10 test subjects after 30 min intravenous infusion of 4.0 g of Bay K and mezlocillin, respectively. The serum concentration course during a period of 10 h showed an open three-compartment model for both antibiotics. The urine recovery of Bay K 4999 during 24 h was only 32.6 +/- 4.3% of the applied dose. In three test subjects with normal renal function, the average renal clearance of Bay K was 61.0, the total serum clearance was 409.2 ml/min/1.73 m2. 31 patients were treated with a daily dose of 3 x 1.0--2.0 g Bay K for severe bronchopulmonary, UTI and cholangiogenic infections. The therapeutic results were good; the relatively high number of side effects should be further investigated in animal studies and require more clinical experience.

摘要

相似文献

1
Clinical pharmacology of a new ureidopenicillin: Bay K 49999.
Chemotherapy. 1980;26(2):81-90. doi: 10.1159/000237887.
2
Comparison of the activities of the new ureidopenicillins piperacillin, mezlocillin, azlocillin, and Bay k 4999 against gram-negative organisms.新型脲基青霉素哌拉西林、美洛西林、阿洛西林和Bay k 4999对革兰氏阴性菌活性的比较。
Antimicrob Agents Chemother. 1979 Aug;16(2):115-9. doi: 10.1128/AAC.16.2.115.
3
Pharmacokinetics of Bay k 4999, a new broad-spectrum penicillin.新型广谱青霉素Bay k 4999的药代动力学
Antimicrob Agents Chemother. 1979 May;15(5):670-3. doi: 10.1128/AAC.15.5.670.
4
[Azlocillin and mezlocillin: two new semisynthetic acylureido-penicillins (author's transl)].阿洛西林和美洛西林:两种新型半合成酰脲类青霉素(作者译)
Infection. 1977;5(3):163-9. doi: 10.1007/BF01639753.
5
[Antibacterial spectrum of mezlocillin and azlocillin, two new antibiotics of the ureidopenicillin group (author's transl)].
Med Clin (Barc). 1982 May 1;78(9):363-71.
6
[In vitro effect of acylureido penicillins and mezlocillin on anaerobic sporeless gram-negative rods of genus Bacteroides].酰脲基青霉素和美洛西林对拟杆菌属无芽孢革兰氏阴性厌氧菌的体外作用
Infection. 1982;10 Suppl 3:S238-43. doi: 10.1007/BF01640681.
7
Dose-dependent pharmacokinetics of azlocillin compared to mezlocillin.与美洛西林相比,阿洛西林的剂量依赖性药代动力学
Chemotherapy. 1982;28(3):160-70. doi: 10.1159/000238071.
8
Pharmacokinetics of azlocillin in healthy subjects.阿洛西林在健康受试者中的药代动力学。
Scand J Infect Dis Suppl. 1981;29:49-54.
9
Studies on the antibacterial activity of two new acylureidopenicillins, mezlocillin and azlocillin.两种新型酰脲类青霉素(美洛西林和阿洛西林)的抗菌活性研究。
Arzneimittelforschung. 1979;29(12a):1932-4.
10
Overview of acylureidopenicillin pharmacokinetics.酰脲类青霉素的药代动力学概述。
Scand J Infect Dis Suppl. 1981;29:33-48.

引用本文的文献

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Comparative pharmacokinetics of two multiple-dose mezlocillin regimens in normal volunteers.两种多次给药美洛西林方案在正常志愿者中的比较药代动力学。
Antimicrob Agents Chemother. 1986 Nov;30(5):675-8. doi: 10.1128/AAC.30.5.675.