An efficient method for gas chromatographic analysis of fosfomycin in plasm
a was developed for preliminary investigations of the bioavailability in po
ultry of 3 commercial complexes of fosfomycin: a levorotatory Ca(-) salt, a
racemic Ca(+/-) salt, and a tromethamine (THAM) salt, The method was used
to determine whether the less expensive racemic mixture would provide equiv
alent levels of fosfomycin in blood as the pure Ca(-) form and the THAM sal
t, The THAM salt, a more expensive product to market, was thought to have t
he greatest bioavailability. The assay is selective, sensitive, and applica
ble to pharmacokinetic analysis.