利用液相色谱-串联质谱法测定牛肉中的激素类促生长剂

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Drug Testing and Analysis Pub Date : 2024-11-19 DOI:10.1002/dta.3827
Mary Mosburg, Yajing Li, Emily Helmes, Tara D Falt, Josephine F Trott, Gina Solomon, Russell C Hovey, Benjamin C Moeller
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引用次数: 0

摘要

在美国,激素类生长促进剂 (HGP) 是一类通常用于牛的药物,目的是提高动物的生长率、改变行为或改善零售肉类的理想特性。令人担忧的是,屠宰后组织中可能会残留低浓度的 HGPs,食用含有这些化合物的组织可能会增加患癌症等不良健康后果的风险。有必要采用灵敏且具有选择性的方法来评估食用可能施用过 HGPs 的动物肉制品的人群接触 HGPs 的情况。本研究开发并验证了一种液相色谱-串联质谱方法,该方法采用高 pH 值溶液进行液液萃取,可检测零售肉类中低浓度的 HGPs,包括雌二醇、睾酮、苯甲酸雌二醇、美伦孕酮、醋酸美伦孕酮、孕酮、丙酸睾酮、群勃龙、醋酸群勃龙和α-玉米赤霉醇,与同类方法相比,所需的肉类质量减少了 30-50 倍。利用氟化铵作为流动相添加剂,无需衍生化,即可实现良好的色谱性能和灵敏度。确定了包括准确度、精密度、回收率、基质效应、检出限、定量限、线性范围和稳定性在内的验证参数。根据化合物的不同,检测限在 0.1 至 1.0 纳克/克之间,具有足够的准确度和精密度,无需大量的样品制备方法。
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Determination of Hormonal Growth Promotants in Beef Using Liquid Chromatography-Tandem Mass Spectrometry.

Hormonal growth promotants (HGPs) are a class of pharmaceutical agents commonly administered to cattle in the United States to improve growth rates of the animal, alter behavior, or to improve the desired characteristics of retail cuts of meat. There is a concern that low residual concentrations of HGPs may remain in tissue after slaughter, and consumption of tissues containing these compounds may increase the risk of adverse health outcomes, including cancer. Sensitive and selective methods are necessary to assess exposure of HGPs by populations that consume meat products from animals that may have been administered HGPs. A liquid chromatography-tandem mass spectrometry method was developed and validated to detect the low-level presence of HGPs including estradiol, testosterone, estradiol benzoate, melengestrol, melengestrol acetate, progesterone, testosterone propionate, trenbolone, trenbolone acetate, and α-zearalanol in retail cuts of meat following a liquid-liquid extraction using a high pH solution with 30-50× less mass of meat required as compared to similar approaches. Good chromatographic performance and sensitivity was achieved utilizing ammonium fluoride as a mobile phase additive without the need for derivatization. Validation parameters including accuracy, precision, recovery, matrix effects, limits of detection, limits of quantitation, linear range, and stability were determined. The limits of detection ranged from 0.1 to 1.0 ng/g, depending on the compound, with adequate accuracy and precision without the need for extensive sample preparation approaches.

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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
期刊最新文献
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