Department of Chemical Pathology, Pathology QLD, Brisbane, Queensland, Australia.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Oct 15;878(28):2863-9. doi: 10.1016/j.jchromb.2010.08.044. Epub 2010 Sep 9.
We describe an ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC MS/MS) method suitable for a routine laboratory to determine endogenous and exogenous glucocorticoids in plasma, plasma ultrafiltrate, urine and saliva in a single analytical run. After addition of a multi-analyte internal standard, a standardised sample preparation procedure with solid phase extraction followed, before injecting into a tandem mass spectrometer with positive mode electron spray ionisation and multiple reactant monitoring acquisition. The chromatography time was 3min. The limit of quantitation for cortisol and cortisone in plasma was 3.75nmol/L and linearity extended to 2000nmol/L. The limit of quantitation for cortisol in plasma ultrafiltrate and saliva was 0.6nmol/L. The limit of quantitation for 11-deoxycortisol and prednisolone was 5nmol/L and for dexamethasone 1nmol/L. The intra-assay CV was <5% and the inter-assay CV <10% for all analytes in all matrices. Comparison with an immuno-assay (IA) plasma cortisol method resulted in a regression equation of UHPLC=0.79×IA+31.12 with R(2)=0.960 (p<0.0001). Comparison with a high performance liquid chromatography (HPLC) cortisol method yielded a regression equation of UHPLC=1.06×HPLC+9.82, R(2)=0.992 (p<0.0001). The simultaneous measurement of endogenous and exogenous glucocorticoids contributed to patient care in cases with dexamethasone and metyrapone dynamic tests and unsuspected therapeutic glucocorticoid use.
我们描述了一种超高效液相色谱-串联质谱(UHPLC-MS/MS)方法,适用于常规实验室,可在单次分析运行中同时测定血浆、血浆超滤物、尿液和唾液中的内源性和外源性糖皮质激素。在加入多分析物内标物后,采用固相萃取标准化样品制备程序,然后注入正离子电喷雾串联质谱仪,采用多反应监测采集。色谱时间为 3 分钟。皮质醇和可的松在血浆中的定量下限为 3.75nmol/L,线性扩展至 2000nmol/L。皮质醇在血浆超滤物和唾液中的定量下限为 0.6nmol/L。11-脱氧皮质醇和泼尼松龙的定量下限为 5nmol/L,地塞米松为 1nmol/L。所有分析物在所有基质中的日内变异系数<5%,日间变异系数<10%。与免疫分析(IA)血浆皮质醇方法的比较得出 UHPLC=0.79×IA+31.12 的回归方程,R(2)=0.960(p<0.0001)。与高效液相色谱(HPLC)皮质醇方法的比较得出 UHPLC=1.06×HPLC+9.82 的回归方程,R(2)=0.992(p<0.0001)。同时测定内源性和外源性糖皮质激素有助于在进行地塞米松和甲吡酮动态试验以及意外使用治疗性糖皮质激素时为患者提供护理。