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四名日本血吸虫感染的菲律宾人血清中硝咪唑及其六种代谢物的浓度-时间过程。

Concentration-time course of niridazole and six metabolites in the serum of four Filipinos with Schistosoma japonicum infection.

作者信息

Valencia C I, Catto B A, Fairchild E H, Wilson S B, Maramba N C, Webster L T

出版信息

J Pharmacol Exp Ther. 1984 Jul;230(1):133-40.

PMID:6547741
Abstract

Niridazole and six of its metabolites have been quantitated by high-pressure liquid chromatography in sera of four male Filipino patients with mild Schistosoma japonicum infections given single oral doses of niridazole (15 mg/kg) on two occasions 10 days apart. Of the five oxidative metabolites measured, 4-hydroxyniridazole and 4-ketoniridazole achieved the highest concentrations, reaching peak values of 0.9 +/- 0.3 microgram/ml of serum (mean +/- S.D., n = 4) and 0.7 +/- 0.1 microgram/ml of serum within 1 to 4 hr. 4-Ketoniridazole achieved peak serum levels 1 hr after the other oxidative metabolites in three of four patients and was the predominant metabolite in the serum of all patients 6 to 10 hr after dosing. By 24 hr, both 4-ketoniridazole and 4-hydroxyniridazole had largely disappeared from the serum. Niridazole and three other oxidative metabolites, 4,5-dihydroxyniridazole, 5-hydroxyniridazole and 4,5-dehydroniridazole, appeared within 1 hr in serum but failed to exceed 0.4 microgram/ml; none of these compounds were detected in the 24-hr serum samples. The pharmacokinetic pattern of niridazole and the oxidative metabolites showed marked interindividual variation but was quite reproducible in the same individual studied 10 days later. 1-Thiocarbamoyl-2-imidazolidinone was analyzed in serum samples by a different high-pressure liquid chromatographic procedure. This reductive metabolite attained maximal levels of 50 to 150 ng/ml of serum 6 to 12 hr after drug administration and remained at 40% or more of its peak concentration even after 24 hr.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对4名轻度日本血吸虫感染的菲律宾男性患者,在间隔10天的两个时间点单次口服硝唑咪(15mg/kg)后,采用高压液相色谱法对其血清中的硝唑咪及其6种代谢产物进行了定量分析。在所测定的5种氧化代谢产物中,4-羟基硝唑咪和4-酮基硝唑咪浓度最高,在1至4小时内血清峰值分别达到0.9±0.3μg/ml(均值±标准差,n = 4)和0.7±0.1μg/ml。4名患者中有3名患者的4-酮基硝唑咪在其他氧化代谢产物之后1小时达到血清峰值水平,给药后6至10小时是所有患者血清中的主要代谢产物。到24小时时,4-酮基硝唑咪和4-羟基硝唑咪在血清中基本消失。硝唑咪和其他3种氧化代谢产物,4,5-二羟基硝唑咪、5-羟基硝唑咪和4,5-脱氢硝唑咪,在血清中1小时内出现,但未超过0.4μg/ml;在24小时血清样本中均未检测到这些化合物。硝唑咪及其氧化代谢产物的药代动力学模式存在明显个体差异,但在10天后对同一患者的研究中具有相当的可重复性。采用不同的高压液相色谱法对血清样本中的1-硫代氨基甲酰基-2-咪唑烷酮进行分析。这种还原代谢产物在给药后6至12小时血清中达到最高水平50至150ng/ml,即使在24小时后仍保持在其峰值浓度的40%或更高。(摘要截短于250字)

相似文献

1
Concentration-time course of niridazole and six metabolites in the serum of four Filipinos with Schistosoma japonicum infection.四名日本血吸虫感染的菲律宾人血清中硝咪唑及其六种代谢物的浓度-时间过程。
J Pharmacol Exp Ther. 1984 Jul;230(1):133-40.
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4-Keto niridazole: a major niridazole metabolite with central nervous system toxicity different than niridazole.4-酮硝唑:一种主要的硝唑代谢产物,具有与硝唑不同的中枢神经系统毒性。
J Pharmacol Exp Ther. 1984 Mar;228(3):662-8.

引用本文的文献

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Susceptibility of Campylobacter species to niridazole.弯曲杆菌属对硝唑咪的敏感性。
Eur J Clin Microbiol. 1986 Dec;5(6):664-5. doi: 10.1007/BF02013295.
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Antibacterial activity of niridazole against Salmonellae.硝唑尼特对沙门氏菌的抗菌活性。
Antimicrob Agents Chemother. 1986 May;29(5):923-4. doi: 10.1128/AAC.29.5.923.
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