首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Use of ultra-high pressure liquid chromatography coupled to high resolution mass spectrometry for fast screening in high throughput doping control
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Use of ultra-high pressure liquid chromatography coupled to high resolution mass spectrometry for fast screening in high throughput doping control

机译:超高压液相色谱与高分辨率质谱联用,用于高通量掺杂控制中的快速筛选

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摘要

We describe a sensitive, comprehensive and fast screening method based on liquid chromatography-high resolution mass spectrometry for the detection of a large number of analytes in sports samples. UHPLC coupled to high resolution mass spectrometry with polarity switching capability is applied for the rapid screening of a large number of analytes in human urine samples. Full scan data are acquired alternating both positive and negative ionisation. Collision-induced dissociation with positive ionisation is also performed to produce fragment ions to improve selectivity for some analytes. Data are reviewed as extracted ion chromatograms based on narrow mass/charge windows (±5. ppm). A simple sample preparation method was developed, using direct enzymatic hydrolysis of glucuronide conjugates, followed by solid phase extraction with mixed mode ion-exchange cartridges. Within a 10. min run time (including re-equilibration) the method presented allows for the analysis of a large number of analytes from most of the classes in the World Anti-Doping Agency (WADA) Prohibited List, including anabolic agents, β_2-agonists, hormone antagonists and modulators, diuretics, stimulants, narcotics, glucocorticoids and β-blockers, and does so while meeting the WADA sensitivity requirements. The high throughput of the method and the fast sample pre-treatment reduces analysis cost and increases productivity. The method presented has been used for the analysis of over 5000 samples in about one month and proved to be reliable.
机译:我们描述了一种基于液相色谱-高分辨率质谱的灵敏,全面,快速的筛选方法,用于检测体育样本中的大量分析物。 UHPLC与具有极性切换功能的高分辨率质谱联用,可用于快速筛查人类尿液样品中的大量分析物。全扫描数据交替获取正电离和负电离。还进行了碰撞诱导的正电离解离,以产生碎片离子,从而提高了对某些分析物的选择性。根据窄的质量/电荷窗口(±5。ppm),将数据作为提取的离子色谱图进行审查。开发了一种简单的样品制备方法,使用葡糖醛酸结合物直接酶促水解,然后用混合模式离子交换柱进行固相萃取。在10分钟的运行时间内(包括重新平衡),所提出的方法可以分析世界反兴奋剂机构(WADA)禁止清单中大多数类别的大量分析物,包括合成代谢药物β_2-激动剂,激素拮抗剂和调节剂,利尿剂,兴奋剂,麻醉剂,糖皮质激素和β受体阻滞剂,并同时满足WADA敏感性要求。该方法的高通量和快速的样品预处理降低了分析成本并提高了生产率。提出的方法已在大约一个月的时间内用于分析5000多个样品,并被证明是可靠的。

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