Application of electrospray ionization hybrid ion trap/time-of-flight mass spectrometry in the rapid characterization of quinocetone metabolites formed in vitro

• Published in: Analytical and bioanalytical chemistry 2010-02, Vol.396 (3), p.1259-1271
• Main Authors: Liu, Zhao-Ying, Huang, Ling-Li, Chen, Dong-Mei, Dai, Meng-Hong, Tao, Yan-Fei, Wang, Yu-Lian, Yuan, Zong-Hui
• Format: Article
• Language: English
• Subjects: Analytical Chemistry; Animals; Biochemistry; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Chromatographic methods and physical methods associated with chromatography; Chromatography, High Pressure Liquid - economics; Chromatography, High Pressure Liquid - methods; Drugs; Exact sciences and technology; Food Science; Fragmentation; High performance liquid chromatography; Hydroxylation; In vitro testing; Ionization; Laboratory Medicine; Male; Mass spectrometry; Metabolites; Microsomes, Liver - metabolism; Molecular Structure; Monitoring/Environmental Analysis; Original Paper; Other chromatographic methods; Quinoxalines - analysis; Quinoxalines - metabolism; Rats; Reduction; Spectrometric and optical methods; Spectrometry, Mass, Electrospray Ionization - economics; Spectrometry, Mass, Electrospray Ionization - methods; Spectrum analysis; Tandem Mass Spectrometry - economics; Tandem Mass Spectrometry - methods; Time Factors
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-009-3245-3

The application of electrospray ionization hybrid ion trap/time-of-flight mass spectrometry coupled with high-performance liquid chromatography (LC/MS–IT–TOF) in the rapid characterization of in vitro metabolites of quinocetone was developed. Metabolites formed in rat liver microsomes were separated using a VP-ODS column with gradient elution. Multiple scans of metabolites in MS and MS 2 modes and accurate mass measurements were automatically performed simultaneously through data-dependent acquisition in only a 30-min analysis. Most measured mass errors were less than 10 ppm for both protonated molecules and fragment ions using external mass calibration. The elemental compositions of all fragment ions of quinocetone and its metabolites could be rapidly assigned based upon the known compositional elements of protonated molecules. The structure of metabolites were elucidated based on the combination of three techniques: agreement between their proposed structure, the accurate masses, and the elemental composition of ions in their mass spectra; comparison of their changes in accurate molecular masses and fragment ions with those of parent drug or metabolite; and the elemental compositions of lost mass numbers in proposed fragmentation pathways. Twenty-seven phase I metabolites were identified as 11 reduction metabolites, three direct hydroxylation metabolites, and 13 metabolites with a combination of reduction and hydroxylation. All metabolites except the N-oxide reduction metabolite M6 are new metabolites of quinocetone, which were not previously reported. The ability to conduct expected biotransformation profiling via tandem mass spectrometry coupled with accurate mass measurement, all in a single experimental run, is one of the most attractive features of this methodology. The results demonstrate the use of LC/MS–IT–TOF approach appears to be rapid, efficient, and reliable in structural characterization of drug metabolites. Figure The accurate extracted mass chromatograms (EIC) of quinocetone metabolites in rat liver microsomes incubated with quinocetone for 2h. M0 quinocetone, M1–M27 metabolites of quinocetone.