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异恶唑基青霉素在人体内的活性代谢产物。

Active metabolites of isoxazolylpencillins in humans.

作者信息

Thijssen H H, Mattie H

出版信息

Antimicrob Agents Chemother. 1976 Sep;10(3):441-6. doi: 10.1128/AAC.10.3.441.

Abstract

Metabolites of the isoxazolylpenicillins that still possessed antibacterial activity were shown to be present in urine and serum. In healthy subjects, the amounts excreted in urine were low; 10 to 23% of the excreted penicillin activities represented the metabolites. The highest amount of metabolite in urine was found for oxacillin, and the lowest was found for flucloxacillin. No extreme differences in the amounts of metabolite excreted were observed when the compounds were administered orally or intravenously. In one healthy subject metabolite levels were estimated for cloxacillin in serum. Very low levels were found, i.e., about 9% of the activity. In subjects with highly impaired renal function, the metabolite may represent up to 50% of the total level of penicillin in serum. The antibacterial activities of the different metabolites were of the same order of magnitude as those of the respective parent compounds. Also, the activity against benzylpenicillin-resistant staphylococci was retained. It is not likely that the formation of the active metabolites should influence therapeutic results.

摘要

具有抗菌活性的异恶唑基青霉素代谢产物在尿液和血清中被检测到。在健康受试者中,尿液中的排泄量较低;排泄的青霉素活性中,10%至23%为代谢产物。尿液中代谢产物含量最高的是苯唑西林,最低的是氟氯西林。口服或静脉给药时,排泄的代谢产物量没有显著差异。在一名健康受试者中,测定了血清中氯唑西林的代谢产物水平。发现其水平极低,即约为活性的9%。在肾功能严重受损的受试者中,代谢产物可能占血清中青霉素总水平的50%。不同代谢产物的抗菌活性与各自母体化合物的抗菌活性处于同一数量级。而且,对耐苄青霉素葡萄球菌的活性得以保留。活性代谢产物的形成不太可能影响治疗效果。

相似文献

1
Active metabolites of isoxazolylpencillins in humans.异恶唑基青霉素在人体内的活性代谢产物。
Antimicrob Agents Chemother. 1976 Sep;10(3):441-6. doi: 10.1128/AAC.10.3.441.
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Bactericidal activity and pharmacology of flucloxacillin.氟氯西林的杀菌活性与药理学
Am J Med Sci. 1976 Jan-Feb;271(1):13-20. doi: 10.1097/00000441-197601000-00002.
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[Active metabolites of oxacillin].
Antibiotiki. 1972 Jan;17(1):27-30.
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FURTHER PHARMACOLOGY AND CHEMOTHERAPY OF CLOXACILLIN.
Br J Pharmacol Chemother. 1963 Oct;21(2):339-54. doi: 10.1111/j.1476-5381.1963.tb01532.x.

本文引用的文献

2
Studies on the formation and activity of the transformation product of ampicillin.
J Antibiot (Tokyo). 1971 Sep;24(9):641-6. doi: 10.7164/antibiotics.24.641.
4
Reversed-phase thin-layer chromatography and partition coefficients of penicillins.
J Chromatogr. 1971 Dec 23;63(2):313-9. doi: 10.1016/s0021-9673(01)85644-2.
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Fate of oral 35S-cloxacillin in man.口服35S-氯唑西林在人体中的转归
Eur J Clin Pharmacol. 1974;7(2):125-31. doi: 10.1007/BF00561326.
9
Pharmacokinetics of flucloxacillin and cloxacillin in healthy subjects and patients on chronic intermittent haemodialysis.
Br J Clin Pharmacol. 1975 Apr;2(2):111-21. doi: 10.1111/j.1365-2125.1975.tb01566.x.

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