Cuervo Darío, Loli Cynthia, Fernández-Álvarez María, Muñoz Gloria, Carreras Daniel
Laboratorio de Control del Dopaje, Agencia Española de Protección de la Salud en el Deporte, Ministerio de Educación, Cultura y Deporte, Gobierno de España, c/El Greco s/n, 28040, Madrid, Spain.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Oct 15;1065-1066:134-144. doi: 10.1016/j.jchromb.2017.08.044. Epub 2017 Sep 5.
A complete analytical protocol for the determination of 25 doping-related peptidic drugs and 3 metabolites in urine was developed by means of accurate-mass quadrupole time-of-flight (Q-TOF) LC-MS analysis following solid-phase extraction (SPE) on microplates and conventional SPE pre-treatment for initial testing and confirmation, respectively. These substances included growth hormone releasing factors, gonadotropin releasing factors and anti-diuretic hormones, with molecular weights ranging from 540 to 1320Da. Optimal experimental conditions were stablished after investigation of different parameters concerning sample preparation and instrumental analysis. Weak cation exchange SPE followed by C18 HPLC chromatography and accurate mass detection provided the required sensitivity and selectivity for all the target peptides under study. 2mg SPE on 96-well microplates can be used in combination with full scan MS detection for the initial testing, thus providing a fast, cost-effective and high-throughput protocol for the processing of a large batch of samples simultaneously. On the other hand, extraction on 30mg SPE cartridges and subsequent target MS/MS determination was the protocol of choice for confirmatory purposes. The methodology was validated in terms of selectivity, recovery, matrix effect, precision, sensitivity (limit of detection, LOD), cross contamination, carryover, robustness and stability. Recoveries ranged from 6 to 70% (microplates) and 17-95% (cartridges), with LODs from 0.1 to 1ng/mL. The suitability of the method was assessed by analyzing different spiked or excreted urines containing some of the target substances.
通过在微孔板上进行固相萃取(SPE)以及分别采用常规SPE预处理进行初始检测和确证,借助精确质量四极杆飞行时间(Q-TOF)液相色谱-质谱分析,开发了一种用于测定尿液中25种与兴奋剂相关的肽类药物和3种代谢物的完整分析方案。这些物质包括生长激素释放因子、促性腺激素释放因子和抗利尿激素,分子量范围为540至1320Da。在研究了有关样品制备和仪器分析的不同参数后,确定了最佳实验条件。弱阳离子交换SPE随后进行C18高效液相色谱和精确质量检测,为所有研究的目标肽提供了所需的灵敏度和选择性。96孔微孔板上的2mg SPE可与全扫描质谱检测结合用于初始检测,从而提供一种快速、经济高效且高通量的方案,可同时处理大量样品。另一方面,30mg SPE柱上的萃取及随后的目标质谱/质谱测定是确证目的的首选方案。该方法在选择性、回收率、基质效应、精密度、灵敏度(检测限,LOD)、交叉污染、残留、稳健性和稳定性方面进行了验证。回收率范围为6%至70%(微孔板)和17%至95%(柱),检测限为0.1至1ng/mL。通过分析含有一些目标物质的不同加标或排泄尿液来评估该方法的适用性。