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建立液质联用和液质质联用法同时测定非法产品中 17 种女性激素的含量。

Simultaneous quantitation of 17 female sex hormones in illegal products by validated liquid chromatography-high resolution mass spectrometry and liquid chromatography-tandem mass spectrometry methods.

机构信息

Center of Advanced Analysis, Ministry of Food and Drug Safety, National Institute of Food and Drug Safety Evaluation, Cheongju, Republic of Korea.

出版信息

J Sep Sci. 2023 Jun;46(11):e2200963. doi: 10.1002/jssc.202200963. Epub 2023 Apr 7.

Abstract

The consumption of food and drugs adulterated with female sex hormones can have an extremely adverse effect on human health. Therefore, developing appropriate monitoring methods for the identification of various exogenous female sex hormones is crucial for minimizing and eliminating the related health risks. Herein, 17 female hormones categorized into two groups: estrogen and progestin, were analyzed using reversed-phase liquid chromatography coupled to Orbitrap or triple quadrupole mass spectrometry. The fragmentation patterns for all compounds were discovered, and fragmented structures were also derived from them through liquid chromatography-high-resolution mass spectrometry followed by qualitative sample analysis. In addition, a quantitative analysis of 67 samples of illicit drugs and dietary supplements was performed using the validated liquid chromatography-tandem mass spectrometry method. Female hormone components were detected in two samples of an unauthorized injectable solution and a tablet-type drug. Medroxyprogesterone was detected in the samples in the range of 96.4-206 ng/g. Notably, eight components similar in structure to steroids were simultaneously detected as male sex hormones by confirming their fragmentation ion patterns using liquid chromatography-high-resolution mass spectrometry. The developed methods thus offer a dependable and practically applicable approach for the screening and detection of exogenous female sex hormones in real food and drug samples to ensure public health.

摘要

食用或使用掺假女性性激素的食物和药物会对人类健康造成极其不利的影响。因此,开发适当的监测方法来识别各种外源性女性性激素对于最大限度地减少和消除相关健康风险至关重要。在此,使用反相液相色谱法结合轨道阱或三重四极杆质谱法对分为雌激素和孕激素两组的 17 种女性激素进行了分析。发现了所有化合物的裂解模式,并通过液相色谱-高分辨率质谱法从它们中推导出了碎裂结构,随后进行了定性样品分析。此外,还使用经过验证的液相色谱-串联质谱法对 67 份非法药物和膳食补充剂样本进行了定量分析。在未经授权的注射溶液和片剂药物的两个样本中检测到了女性激素成分。在这些样品中,检测到的美孕酮含量在 96.4-206ng/g 范围内。值得注意的是,通过使用液相色谱-高分辨率质谱法确认其碎裂离子模式,同时检测到了 8 种与甾体结构相似的作为男性性激素的成分。因此,所开发的方法为筛选和检测实际食物和药物样本中的外源性女性性激素提供了可靠且实用的方法,以确保公众健康。

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