Infant formula samples mere analysed to determine their free L-carniti
ne content by using flow injection (FI) with an incorporated immobilis
ed carnitine acetyltransferase bioreactor. The methodology was based o
n the spectrophotometric determination through its reaction with carni
tine acetyltransferase coupled with acetyl coenzyme A (acetyl-CoA) and
dithiobenzoate. The merging zones technique was used to minimise acet
yl CoA consumption. Linearity was observed over the concentration rang
e 10-80 mg l(-1) with L-carnitine as standard (r = 0.9998) and the rat
e of analysis was 50 h(-1) infant formula samples. The enzymic FI meth
od afforded a low RSD (2.2%). Comparisons were made with other methods
of known accuracy. The enzymic reactors were stable for 3 months when
used daily at the optimum pH.