We have evaluated a tandem mass spectrometry method for determining free ca
rnitine concentrations in plasma and have compared its performance with tha
t of an existing radioenzymatic assay. In this method, plasma was mixed wit
h an internal standard, carnitine-d(3) (600 nmol/L), and butylated before a
nalysis on a Quattro II tandem mass spectrometer.
The detection limit of the tandem mass spectrometric (MS) method was 4 mu m
ol/L and carryover between samples was 2.2%. Precision of the method was 1.
6 5.4% between injections and 4.0-5.6% between samples. Between batch preci
sion was 10 13%.
The method was linear up to a free carnitine concentration of 300 mu mol/L
and good agreement was found with the existing radioenzymatic assay.
We conclude that the tandem MS method is a precise and robust method for th
e determination of free carnitine concentrations in plasma that overcomes t
he disadvantages of the radiochemical method.