A-038 An Improved Multiplexed HTLC-HESI-MSMS Method for the Measurement of Total Testosterone in Serum

Abstract Background Testosterone is an anabolic steroid produced primarily in the testicles of males and mainly in the ovaries of females. Imbalance of testosterone is the primary cause of hypogonadism in males, hirsutism and virilization in females, osteoporosis, and diabetes mellitus. Accurate and fast-turnaround measurement of testosterone is critical for diagnosis, prevention, and treatment of testosterone-related diseases in adults and children. In a previous study, testosterone was derivatized with methoxyamine and hydroxylamine in a multiplexed high turbulence liquid chromatography with heated-electrospray ionization-tandem mass spectrometry (HTLC-HESI-MS/MS) method. Using these reagents, differential mass-tagging of testosterone allowed different specimens to be combined in a single injection to increase assay throughput. However, interference was observed for hydroxylamine-derivatized testosterone in serum collected in serum separator tubes (SST). In the current study, our objectives were to (1) replace hydroxylamine with a new derivatizing agent not subject to interference and (2) develop an improved HTLC-HESI-MS/MS method for multiplexed total testosterone measurement. Methods Healthy male and female donor specimens were collected in SST and red-top tubes. Serum was mixed with stable isotope-labeled testosterone as internal standard (ISTD) prior to protein precipitation. Testosterone in the supernatants was derivatized, enriched by solid phase extraction, dried, and reconstituted. Specimens were injected on the HTLC system for on-line extraction, transferred to analytical columns, and eluted using binary gradient. Testosterone derivatives and ISTDs were detected and analyzed on a Triple Quadrupole Mass Spectrometer (Thermo) equipped with HESI. Ionization and multiple reaction monitoring (MRM) scan parameters were optimized for maximized ion transmission and sensitive, specific, and stable quantitation. MRM transitions were used as quantifiers and qualifiers for both testosterone derivatives. Also assessed were ion suppression using T-column infusion, specimen stability by storage in SST tubes at 4 °C, isobaric interference from dehydroepiandrosterone (DHEA), and carryover. Results Intra- and inter-assay coefficients of variation (CV%) for total testosterone levels were