利用 HPLC-ESI-TOF 测定奶粉中全分子的热稳定直接溶血素

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Hong-Na Li, Tao Wang, Zhao-di Kang, Yan-Ge Yang, Tao Li, Fei Yuan
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引用次数: 0

摘要

虽然副溶血性弧菌(V. parahaemolyticus)是一种经常在海产品中发现的病原体,但也有可能存在于乳制品等其他食品中。副溶血性弧菌的主要致病因子是热稳定性直接溶血素(TDHs),它是一种致命毒素,因此有必要建立定性和定量测定 TDHs 的方法。我们采用 HPLC-ESI-TOF 技术建立了 TDHs 的鉴定方法。HPLC-ESI-TOF 对 TDHs 的鉴定和定量离子进行了确认。该方法的检出限为0.20~0.40 mg/kg,定量限为0.5~1.0 mg/kg,所有TDHs的回收率为78%~94%,相对标准偏差小于10%。这项研究将为开发HPLC-MS/MS检测食品样品中TDHs的方法提供参考,为政府监测食品中的TDHs污染提供工具。
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 Whole Molecular of Thermostable Direct Hemolysins in Milk Powder by HPLC-ESI-TOF.

Although Vibrio parahaemolyticus (V. parahaemolyticus) is a pathogen frequently found in seafood, there is a possibility of its presence in other foods, such as dairy products. The main virulence factors of V. parahaemolyticus are thermostable direct hemolysins (TDHs) which are lethal toxins, so it is necessary to establish qualitative and quantitative methods for determining TDHs. HPLC-ESI-TOF was employed to establish a method for identifying TDHs. The identification and quantification ions of TDHs were confirmed by HPLC-ESI-TOF. The method was developed for detecting TDHs in milk powder using HPLC-ESI-TOF in this paper, and limits of detection (were between 0.20 and 0.40 mg/kg, limits of quantitation were between 0.5 and 1.0 mg/kg and recoveries of all TDHs were between from 78% to 94% with relative standard deviation lower than 10%. This research will provide a reference for developing methods of HPLC-MS/MS to detect TDHs in food samples, which can provide a tool for the government to monitor TDHs contamination in foods.

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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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