Kolmonen Marjo, Leinonen Antti, Pelander Anna, Ojanperä Ilkka
Forensic Toxicology Division, Department of Forensic Medicine, University of Helsinki, Finland.
Anal Chim Acta. 2007 Feb 28;585(1):94-102. doi: 10.1016/j.aca.2006.12.028. Epub 2006 Dec 23.
A general screening method based on solid phase extraction (SPE) and liquid chromatography/time-of-flight mass spectrometry (LC/TOFMS) was developed and investigated with 124 different doping agents, including stimulants, beta-blockers, narcotics, beta(2)-adrenergic agonists, agents with anti-estrogenic activity, diuretics and cannabinoids. Mixed mode cation exchange/C8 cartridges were applied to SPE, and chromatography was based on gradient elution on a C18 column. Ionization of the analytes was achieved with electrospray ionization in the positive mode. Identification by LC/TOFMS was based on retention time, accurate mass and isotopic pattern. Validation of the method consisted of analysis of specificity, analytical recovery, limit of detection and repeatability. The minimum required performance limit (MRPL), established by World Anti-Doping Agency (WADA), was attained to 97 doping agents. The extraction recoveries varied between 33 and 98% and the median was 58%. Mass accuracy was always better than 5 ppm, corresponding to a maximum mass error of 0.7 mDa. The repeatability of the method for spiked urine samples, expressed as median of relative standard deviations (RSD%) at concentrations of MRPL and 10 times MRPL, were 14% and 9%, respectively. The suitability of the LC/TOFMS method for doping control was demonstrated with authentic urine samples.
开发了一种基于固相萃取(SPE)和液相色谱/飞行时间质谱(LC/TOFMS)的通用筛查方法,并对124种不同的兴奋剂进行了研究,包括兴奋剂、β受体阻滞剂、麻醉品、β₂肾上腺素能激动剂、具有抗雌激素活性的药物、利尿剂和大麻素。混合模式阳离子交换/C8柱用于SPE,色谱基于C18柱上的梯度洗脱。分析物通过正模式电喷雾电离实现电离。通过LC/TOFMS进行的鉴定基于保留时间、精确质量和同位素模式。该方法的验证包括特异性分析、分析回收率、检测限和重复性分析。世界反兴奋剂机构(WADA)设定的最低所需性能限制(MRPL)对97种兴奋剂得以实现。萃取回收率在33%至98%之间,中位数为58%。质量准确度始终优于5 ppm,对应最大质量误差为0.7 mDa。加标尿液样品方法的重复性,以MRPL浓度和10倍MRPL浓度下相对标准偏差(RSD%)的中位数表示,分别为14%和9%。用真实尿液样品证明了LC/TOFMS方法在兴奋剂检测中的适用性。