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高效液相色谱法测定生物材料中一种新型β-内酰胺酶抑制剂及其代谢产物与哌拉西林联合治疗时的含量

High-performance liquid chromatographic determination of a new beta-lactamase inhibitor and its metabolite in combination therapy with piperacillin in biological materials.

作者信息

Marunaka T, Maniwa M, Matsushima E, Minami Y

机构信息

Biological Research Laboratory, Taiho Pharmaceutical Co., Ltd., Tokushima, Japan.

出版信息

J Chromatogr. 1988 Sep 23;431(1):87-101. doi: 10.1016/s0378-4347(00)83072-8.

DOI:10.1016/s0378-4347(00)83072-8
PMID:2853169
Abstract

[2S-(2 alpha,3 beta,5 alpha)]-3-Methyl-7-oxo-3-(1H-1,2,3-triazol-1-yl- methyl)-4-thia-1-azabicyclo [3.2.0]-heptane-2-carboxylic acid 4,4-dioxide (YTR-830H) is a new beta-lactamase inhibitor and the combination therapy of this compound with piperacillin is now under study. For the determination of the beta-lactamase inhibitor and piperacillin in biological materials, plasma and visceral tissue homogenates were deproteinized, whereas diluted urine and filtered faeces homogenates were treated with a Sep-Pak C18 cartridge. In order to assay the inactive metabolite of beta-lactamase inhibitor, each sample was treated with a Sep-Pak C18 cartridge. Aliquots of each preparation were chromatographed using ion-pair and reversed-phase chromatographic techniques on a high-performance liquid chromatograph equipped with a UV detector, set at 220 nm. The detection limits of beta-lactamase inhibitor and piperacillin were 0.2 microgram/ml in plasma, 2.5-5.0 micrograms/ml in urine and 0.2-0.5 microgram/g in visceral tissue and faeces. Those of the metabolite were 1.0 microgram/ml in plasma, 2.5-5.0 micrograms/ml in urine and 1.0 microgram/g in visceral tissue and faeces. A precise and sensitive assay for the determination of the beta-lactamase inhibitor, its metabolite and piperacillin is described, and their stabilities in several media are reported.

摘要

[2S-(2α,3β,5α)]-3-甲基-7-氧代-3-(1H-1,2,3-三唑-1-基甲基)-4-硫杂-1-氮杂双环[3.2.0]庚烷-2-羧酸4,4-二氧化物(YTR-830H)是一种新型β-内酰胺酶抑制剂,目前正在研究该化合物与哌拉西林的联合治疗。为了测定生物材料中的β-内酰胺酶抑制剂和哌拉西林,血浆和内脏组织匀浆进行了脱蛋白处理,而稀释尿液和过滤后的粪便匀浆则用Sep-Pak C18柱进行处理。为了测定β-内酰胺酶抑制剂的无活性代谢物,每个样品都用Sep-Pak C18柱进行处理。每种制剂的等分试样在配备紫外检测器(设定在220nm)的高效液相色谱仪上,使用离子对和反相色谱技术进行色谱分析。β-内酰胺酶抑制剂和哌拉西林的检测限在血浆中为0.2微克/毫升,在尿液中为2.5 - 5.0微克/毫升,在内脏组织和粪便中为0.2 - 0.5微克/克。代谢物的检测限在血浆中为1.0微克/毫升,在尿液中为2.5 - 5.0微克/毫升,在内脏组织和粪便中为1.0微克/克。本文描述了一种用于测定β-内酰胺酶抑制剂、其代谢物和哌拉西林的精确且灵敏的分析方法,并报告了它们在几种介质中的稳定性。

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