Ventura Rosa, Roig M, Montfort N, Sáez P, Bergés Rosa, Segura Jordi
Grup de Recerca en Bioanàlisis, IMIM-Hospital del Mar, Barcelona, Spain.
Eur J Mass Spectrom (Chichester). 2008;14(3):191-200. doi: 10.1255/ejms.920.
The reliability of ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC- MS/MS) for high throughput screening in anti-doping control has been tested. A method to screen for the presence of diuretics and other doping agents in urine has been optimised and validated. The extraction procedure consisted of an alkaline extraction (pH 9.5) with ethyl acetate and salting-out effect (sodium chloride). The extracts were analysed by UPLC-MS/MS. Analysis of 34 forbidden drugs and metabolites was achieved in a total run time of 5 min, using a C18 column (100 mm x 2.1 mm i.d., 1.7 microm particle size) and a mobile phase containing deionised water and acetonitrile with formic acid, with gradient elution at a flow-rate of 0.6 mL min(-1). Identification of the compounds was performed by multiple reaction monitoring, using electrospray ionisation in positive- or negative-ion mode. Precursor and product ions were studied for each compound and cone voltage and collision energy were optimised. Due to the different chemical structure of the compounds under study, extraction recoveries varied from less than 10% to 100% depending on the analyte. The limits of detection ranged from 50 ng mL(-1) to 200 ng mL(-1), and all the compounds comply with the requirements of quality established by the World Anti-doping Agency. Intra-assay precision was evaluated at two concentrations for each compound and, in most cases, a relative standard deviation of the signal ratio lower than 20% was obtained. The method has demonstrated to be reliable when analysing routine samples and the short analysis time resulting from a simple sample preparation and a rapid instrumental analysis allow a fast turn-around time and makes it of great interest for routine anti-doping control purposes.
超高效液相色谱-串联质谱法(UPLC-MS/MS)在反兴奋剂控制高通量筛查中的可靠性已得到测试。一种用于筛查尿液中利尿剂和其他兴奋剂的方法已得到优化和验证。提取程序包括用乙酸乙酯进行碱性提取(pH 9.5)和盐析效应(氯化钠)。提取物通过UPLC-MS/MS进行分析。使用C18柱(100 mm×2.1 mm内径,1.7微米粒径)和含有去离子水、乙腈和甲酸的流动相,以0.6 mL min⁻¹的流速进行梯度洗脱,在5分钟的总运行时间内实现了对34种违禁药物和代谢物的分析。化合物的鉴定通过多反应监测进行,采用正离子或负离子模式的电喷雾电离。对每种化合物研究了前体离子和产物离子,并优化了锥孔电压和碰撞能量。由于所研究化合物的化学结构不同,提取回收率根据分析物的不同从低于10%到100%不等。检测限范围为50 ng mL⁻¹至200 ng mL⁻¹,所有化合物均符合世界反兴奋剂机构规定的质量要求。在每个化合物的两个浓度下评估了批内精密度,在大多数情况下,信号比的相对标准偏差低于20%。该方法在分析常规样品时已证明是可靠的,简单的样品制备和快速的仪器分析所产生的短分析时间允许快速周转,使其对于常规反兴奋剂控制目的具有极大的吸引力。