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采用柱切换液相色谱法测定脂肪组织和血清中他唑巴坦和哌拉西林的新型快速全自动方法。

New and rapid fully automated method for determination of tazobactam and piperacillin in fatty tissue and serum by column-switching liquid chromatography.

作者信息

Trittler R, Ehrlich M, Galla T J, Horch R E, Kümmerer K

机构信息

Institute of Environmental Medicine and Hospital Epidemiology, Hugstetter Str. 55, D 79106 Freiburg i. Br., Germany.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Aug 5;775(2):127-32. doi: 10.1016/s1570-0232(02)00298-2.

Abstract

A sensitive and rapid HPLC assay for determining tazobactam and piperacillin in fatty tissue and serum is described. While the common methods need liquid-liquid extraction before the injection in a automated column switching HPLC, the new method works by direct injection of the filtered tissue extract or diluted serum in a automated column switching HPLC without any other pre-treatment. This was performed by the use of a NH2-precolumn and enrichment/transfer at different pH-level. During the analyses, the NH2-precolumn was automatically regenerated with acetonitrile-water. The chromatogram peaks for piperacillin and tazobactam were identified by the retention time and quantified by peak area. The calibration curve was linear between 1 and 16 microg/ml. The quantification limit of tazobactam was about 1 microg/ml in fatty tissue extracts and in diluted serum (calculated for pure serum 2 microg/ml), respectively. For piperacillin it was less. The described procedure allows sample clean-up and determination of the antibiotic within 35 min. The chromatograms with this easy sample treatment had the same quantity of matrix peaks and in contrast to liquid-liquid extraction no loss of piperacillin. Because of the automatically rinsing of the NH2-precolumn during the chromatographic separation, more than 50 different biological samples could be measured with one NH2-precolumn without loss of performance.

摘要

本文描述了一种灵敏且快速的高效液相色谱法(HPLC),用于测定脂肪组织和血清中的他唑巴坦和哌拉西林。常见方法在自动柱切换HPLC进样前需要液液萃取,而新方法通过直接将过滤后的组织提取物或稀释血清注入自动柱切换HPLC中,无需任何其他预处理即可工作。这是通过使用NH2预柱并在不同pH水平下进行富集/转移来实现的。在分析过程中,NH2预柱用乙腈-水自动再生。哌拉西林和他唑巴坦的色谱峰通过保留时间进行鉴定,并通过峰面积进行定量。校准曲线在1至16μg/ml之间呈线性。他唑巴坦在脂肪组织提取物和稀释血清中的定量限分别约为1μg/ml(按纯血清计算为2μg/ml)。哌拉西林的定量限更低。所述方法可在35分钟内完成样品净化和抗生素测定。采用这种简单样品处理方法得到的色谱图具有相同数量的基质峰,与液液萃取相比,哌拉西林没有损失。由于在色谱分离过程中NH2预柱会自动冲洗,一个NH2预柱可测定超过50个不同的生物样品而不会损失性能。

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