利用固相萃取和超临界流体色谱-串联质谱法测定水中的大环内酯类药物。

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Denis V. Ovchinnikov, Sergey A. Vakhrameev, Ilya S. Voronov, Marina P. Semushina, Nikolay V. Ul'yanovskii, Dmitry S. Kosyakov
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引用次数: 0

摘要

大环内酯类化合物是一类用于治疗人类和动物细菌感染的化合物。大环内酯类化合物的广泛使用造成了水环境的污染,一方面对水生生物产生有害影响,另一方面可能导致耐药微生物菌株的出现。综上所述,有必要对环境,尤其是水体中的这些化合物进行监测。通常采用高效液相色谱法结合串联质谱法来解决这一问题,然而,这项工作显示了采用超临界流体色谱-串联质谱法的可能性。该研究开发了一种测定四种常见大环内酯类药物(即红霉素、克拉霉素、米德霉素和交沙霉素)的方法。该方法采用固相萃取,定量限为 0.57-6.8 纳克/升。所提出的方法在一个真实对象(城市污水样本)上进行了验证和测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of Macrolides in Water Using Solid-Phase Extraction and Supercritical Fluid Chromatography-Tandem Mass Spectrometry

Macrolides are a group of compounds used to treat bacterial infections in humans and animals. Their widespread use results in the contamination of the water environment, which, on the one hand, has a detrimental effect on aquatic organisms and, on the other hand, can lead to the emergence of resistant strains of microorganisms. All of the above determines the need for monitoring of these compounds in the environment, particularly, in water objects. Usually, the high-performance liquid chromatography combined with tandem mass spectrometry method is used to solve this problem, however, this work shows the possibility of using the supercritical fluid chromatography-tandem mass spectrometry method. An approach for the determination of four common macrolides, namely erythromycin, clarithromycin, midecamycin, and josamycin, was developed. The use of solid-phase extraction allowed to achieve limits of quantification at 0.57–6.8 ng/L. The presented approach was validated and tested on a real object—a sample of municipal wastewater.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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