Performance characteristics of a novel tandem mass spectrometry assay for serum testosterone.

Abstract:

BACKGROUND:Commercial immunoassays for testosterone (Te) may give inaccurate results for samples from women and children, leading to misdiagnosis and inappropriate treatment. We developed a sensitive and specific tandem mass spectrometric assay for measurement of Te at the concentrations encountered in women and children. METHODS:Te was extracted with methyl tert-butyl ether from 100 microL of serum or plasma, derivatized to form an oxime, and reextracted by solid-phase extraction. Instrumental analysis was performed on an API 4000 HPLC tandem mass spectrometer in the multiple-reaction monitoring (MRM) mode. The MRM transitions (m/z) were 304-->124 and 304-->112 for Te and 307-->124 and 307-->112 for d3-Te. RESULTS:Within- and between-run CVs were <12% and 7.9%, respectively. The limit of quantification was 0.0346 nmol/L (1 ng/dL). Reference intervals for sex hormone-binding globulin and total, free, and bioavailable Te were established for children of Tanner stages 1 through 5 and adult males and females. CONCLUSIONS:The sensitivity and specificity of the method are adequate for analysis of Te in samples from women and children. The method requires small sample volumes, has adequate precision, and is not subject to interferences.

journal_name

Clin Chem

journal_title

Clinical chemistry

authors

Kushnir MM,Rockwood AL,Roberts WL,Pattison EG,Bunker AM,Fitzgerald RL,Meikle AW

doi

10.1373/clinchem.2005.052167

subject

Has Abstract

pub_date

2006-01-01 00:00:00

pages

120-8

issue

1

eissn

0009-9147

issn

1530-8561

pii

clinchem.2005.052167

journal_volume

52

pub_type

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