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- Title
Testosterone measurement by liquid chromatography tandem mass spectrometry: the importance of internal standard choice.
- Authors
Owen, L. J.; Keevil, B. G.
- Abstract
Background: Testosterone measurement by liquid chromatography tandem mass spectrometry (LC-MS/MS) is well accepted as the preferred technique for the analysis of testosterone. Variation is seen between assays and is likely to be due to method differences. One area of inconsistency among assays is the choice of internal standard. We investigated the effects of three internal standards. Methods: Testosterone with two deuterium (D2), five deuterium (D5) and three carbon 13 enrichment (C13) were separately assessed. Samples were extracted using ether following the addition of 10 μL of internal standard. All aliquots were prepared in triplicate, one for each type of internal standard. After mixing, the ether was transferred to a 96-deep well block, and then evaporated to dryness. Extracts were reconstituted with 50% mobile phases and analysed using a Waters ACQUITY UPLC and Quattro Premier tandem mass spectrometer. This method had previously been shown to have excellent agreement with a reference method using the D2 internal standard and this was considered the target. Results: Lower results were obtained when using D5 testosterone when compared with D2 testosterone. The C13 internal standard also gave lower results, but was closer to the D2 target than the D5 internal standard. Conclusions: The choice of internal standard alone can have a significant affect on the results obtained by LC-MS/MS assays for testosterone using this chromatography. The effects of the combination of chromatography and internal standard choice should be investigated during method development.
- Subjects
TESTOSTERONE; LIQUID chromatography-mass spectrometry; DEUTERIUM; MASS spectrometers; CHROMATOGRAPHIC analysis; MATRIX effect; SOLID phase extraction; SERUM
- Publication
Annals of Clinical Biochemistry, 2012, Vol 49, Issue 6, p600
- ISSN
0004-5632
- Publication type
Article
- DOI
10.1258/acb.2012.012037