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高分辨准确质量数筛查和液相色谱-串联质谱法对“天然”草药补充剂中活性药物成分的确认应用

Application of HRAM screening and LC-MS/MS confirmation of active pharmaceutical ingredient in "natural" herbal supplements.

作者信息

Pascali Jennifer P, Fais Paolo, Vaiano Fabio, Bertol Elisabetta

机构信息

Forensic Toxicology Division, Department of Health Sciences, University of Florence, Largo Brambilla 3, 50134, Florence, Italy.

University of Bologna, Department of Medical and Surgical Sciences, Unit of Legal Medicine, Via Irnerio 49, Bologna, Italy.

出版信息

Forensic Sci Int. 2018 May;286:e28-e31. doi: 10.1016/j.forsciint.2018.03.014. Epub 2018 Mar 16.

Abstract

The growing market of herbal remedies worldwide could pose severe problems to consumers' health due to the possible presence of potentially harmful, undeclared synthetic substances or analogues of prescription drugs. The present work shows a simple but effective approach to unequivocally identify synthetic anorectic compounds in allegedly 'natural' herbal extracts, by exploiting liquid chromatography/time of flight (Q-TOF LC/MS) technology coupled to liquid chromatography/triple quadrupole (LC-MS/MS) confirmation and quantitation. The procedure was applied to five tea herbal extracts and pills sold as coadjutant for weigh loss. The method exploited liquid-liquid sample extraction (LLE) and separation in a C18 (2.1mm×150mm, 1.8μm) column. QTOF acquisitions were carried out both in scan mode and all ion MS/MS mode and results were obtained after search against ad hoc prepared library. Sibutramine, 4-hydroxyamphetamine, caffeine and theophylline were preliminary identified samples. Confirmation and quantitation of the preliminary identified compounds were obtained in LC-MS/MS after preparation of appropriated standards. Sibutramine, caffeine and theophylline were finally confirmed and quantitate.

摘要

由于所谓“天然”草药提取物中可能存在潜在有害的未申报合成物质或处方药类似物,全球草药市场的不断增长可能会给消费者健康带来严重问题。本研究展示了一种简单而有效的方法,通过利用液相色谱/飞行时间(Q-TOF LC/MS)技术与液相色谱/三重四极杆(LC-MS/MS)的确证和定量相结合,明确鉴定据称“天然”草药提取物中的合成食欲抑制剂化合物。该程序应用于五种作为减肥辅助剂出售的茶草药提取物和药丸。该方法采用液-液样品萃取(LLE),并在C18(2.1mm×150mm,1.8μm)柱上进行分离。QTOF采集在扫描模式和全离子MS/MS模式下进行,结果是在与专门制备的库进行比对后获得的。西布曲明、4-羟基苯丙胺、咖啡因和茶碱是初步鉴定出的样品。在制备适当标准品后,通过LC-MS/MS对初步鉴定出的化合物进行确证和定量。最终确证并定量了西布曲明、咖啡因和茶碱。

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