DETERMINATION OF XANOMELINE AND ACTIVE METABOLITE, N-DESMETHYLXANOMELINE, IN HUMAN PLASMA BY LIQUID-CHROMATOGRAPHY ATMOSPHERIC-PRESSURE CHEMICAL-IONIZATION MASS-SPECTROMETRY

We have developed a method for the determination of xanomeline and its pharmacologically active N-desmethyl metabolite. The validated method uses hexane to extract xanomeline and its N-desmethyl metabolite from basified plasma. The hexane extract is dried, reconstituted, and anal yzed using a liquid chromatographic-atmospheric pressure chemical ioni zation tandem mass spectrometry system. The method was developed to su pport phase II clinical trials and has proven to be extremely sensitiv e, fast, and rugged. The method has a limit of quantitation of 75 and 200 pg/ml plasma for xanomeline and the N-desmethyl metabolite, respec tively. Sample analysis times were less than 3 min from one injection to the next.