Tai Susan S-C, Welch Michael J
Analytical Chemistry Division, National Institute of Standards and Technology, Gaithersburg, MD 20899-8392, USA.
Anal Chem. 2004 Feb 15;76(4):1008-14. doi: 10.1021/ac034966f.
Cortisol is an important diagnostic marker for the production of steroid hormones, and accurate measurements of serum cortisol are necessary for proper diagnosis of adrenal function. A candidate reference method involving isotope dilution coupled with liquid chromatography/mass spectrometry (LC/MS) and liquid chromatography/tandem mass spectrometry (LC/MS/MS) has been developed and critically evaluated. An isotopically labeled internal standard, cortisol-d(3), was added to serum, followed by equilibration and solid-phase and ethyl acetate extractions to prepare samples for liquid chromatography/mass spectrometry electrospray ionization (LC/MS-ESI) and liquid chromatography/tandem mass spectrometry electrospray ionization (LC/MS/MS-ESI) analyses. (M + H)(+) ions at m/z 363 and 366 for cortisol and its labeled internal standard were monitored for LC/MS. The transitions of (M + H)(+) --> [(M + H)(+) - 2H(2)O] at m/z 363 --> 327 and 366 --> 330 were monitored for LC/MS/MS. The accuracy of the measurement was evaluated by a comparison of results of this candidate reference method on lyophilized human serum reference materials for cortisol [Certified Reference Materials 192 and 193] with the certified values determined by gas chromatography/mass spectrometry reference methods and by a recovery study for the added cortisol. The results of this method for total cortisol agreed with the certified values within 1.1%. The recovery of the added cortisol ranged from 99.8% to 101.0%. This method was applied to the determination of cortisol in samples of frozen serum pools. Excellent precision was obtained with within-set CVs of 0.3%-1.5% and between-set CVs of 0.04%-0.4% for both LC/MS and LC/MS/MS analyses. The correlation coefficients of all linear regression lines ranged from 0.998 to 1.000. The detection limits (at a signal-to-noise ratio of approximately 3-5) were 10 and 15 pg for LC/MS and LC/MS/MS, respectively. This method, which demonstrates good accuracy and precision, and is free from interferences from structural analogues, qualifies as a candidate reference method and can be used as an alternative reference method to provide an accuracy base to which the routine methods can be compared.
皮质醇是类固醇激素产生的重要诊断标志物,准确测量血清皮质醇对于正确诊断肾上腺功能至关重要。一种涉及同位素稀释与液相色谱/质谱联用(LC/MS)和液相色谱/串联质谱联用(LC/MS/MS)的候选参考方法已被开发并进行了严格评估。将同位素标记的内标物皮质醇 - d(3) 添加到血清中,然后进行平衡以及固相和乙酸乙酯萃取,以制备用于液相色谱/质谱电喷雾电离(LC/MS - ESI)和液相色谱/串联质谱电喷雾电离(LC/MS/MS - ESI)分析的样品。在LC/MS分析中监测皮质醇及其标记内标物在m/z 363和366处的(M + H)(+)离子。在LC/MS/MS分析中监测m/z 363 --> 327和366 --> 330处的(M + H)(+) --> [(M + H)(+) - 2H₂O]跃迁。通过将该候选参考方法对皮质醇冻干人血清参考物质[认证参考物质192和193]的结果与气相色谱/质谱参考方法确定的认证值进行比较以及对添加皮质醇的回收率研究,来评估测量的准确性。该方法测定总皮质醇的结果与认证值的偏差在1.1%以内。添加皮质醇的回收率范围为99.8%至101.0%。该方法应用于冷冻血清库样品中皮质醇的测定。对于LC/MS和LC/MS/MS分析,组内变异系数(CV)为0.3% - 1.5%,组间变异系数为0.04% - 0.4%,获得了出色的精密度。所有线性回归线的相关系数范围为0.998至1.000。LC/MS和LC/MS/MS的检测限(信噪比约为3 - 5时)分别为10和15 pg。该方法具有良好的准确性和精密度,且不受结构类似物的干扰,符合候选参考方法的条件,可作为替代参考方法为常规方法提供可比较的准确性基础。