کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1968440 | 1538860 | 2016 | 6 صفحه PDF | دانلود رایگان |
• Mass spectrometry is considered the gold standard for steroid hormone analysis (because of its accuracy and sensitivity)
• An LC-MS/MS method for analysis of 17-hydroxyprogesterone, androstenedione, testosterone and cortisol is proposed
• Turboflow chromatography guarantee an efficient purification from the matrix component
• the comparison with immunoassay indicates an acceptable correlation except for low level of testosterone
• The presented method is suitable for routine clinical laboratory
BackgroundThe simultaneous quantification of a steroid hormones panel provides more clinical information than a single steroid assay. Traditionally, steroids have been quantified with immunoassays which are characterized by high rate of positive results. Aim of this work, was to develop a TurboFlow-LC-MS/MS method for the simultaneous quantification of 17-hydroxyprogesterone, androstenedione, cortisol and testosterone in serum.MethodsTo 100 μL of serum, 100 μL of internal standard solution in methanol were added; after centrifugation the supernatant was injected in the TurboFlow for further purification. Steroids were determined using a TSQ Vantage operating with an atmospheric pressure chemical ionization source. Method was fully validated and results compared with immunoassay methods.ResultsLimit of quantification ranged from 0.02 ng/mL to 1 ng/mL. The precision was lower than 11% and accuracy ranged from 93.5 to 121.6%. The correlation was acceptable for all analytes except for low levels of testosterone. However, the Bland-Altman plots display a positive bias for androstenedione and 17-hydroxyprogesterone, and a negative bias for cortisol and testosterone.ConclusionsTurboFlow analysis provides a simple and effective clean-up procedure minimizing the interference of the matrix. The presented method is selective, precise, and sensitive being suitable in a clinical laboratory.
Journal: Clinical Biochemistry - Volume 49, Issues 13–14, September 2016, Pages 998–1003