Separation and Determination of Diastereomeric Flurbiprofen A cyl Glucuronides in Human Urine by LC/ESI-MS with a Simple Column-Switching Technique

Endogenous and exogenous compounds having a carboxyl group, such as a-arylpropionic acid derivatives, undergo a phase 11 metabolic reaction to produce an amino acid conjugate through the acyl COA thioester as well as the acyl glucuronide. It was previously shown that flurbiprofen, one of the nonsteroidal anti-inflammatory drugs, is not subjected to activation of the carboxyl group by the COA thioester ligase, suggesting that acyl glucuronidation is the main phase 11 metabolic pathway. Recent ob-servations, however, have demonstrated that the nonenzymatic formation of a covalently protein-bound drug, which is produced by the action of the acyl glucuronide, may cause hypersensitive reactions. Ac-cordingly, a reliable method to measure diastereomeric flurbiprofen glucuronides in human biological fluids is required. In this study, we describe a liquid chromatographic/mass spectrometric method with a simple column switching technique to determine diastereomeric flurbiprofen acyl glucuronides in human urine specimens. The optimal conditions for the electrospray ionization were established based on the effects of orifice and ring lens voltages as well as mobile phase additives. The proposed method applied to urine specimens demonstrates high accuracy and reproducibility for the determination of flurbiprofen glucuronides in a quantitative range from 0. 74 to 146. 5pg/mL, with a detection limit of 7. 4pg (17. 6 fmol)/injection of S-fiurbiprofen glucuronide, at a signal-to-noise ratio of 10 under the selected ion-monitoring mode. The urinary concentration of R-flurbiprofen glucuronides in healthy subjects deter-mined by the proposed method were 6. 8-29. 4 pg/mL, and those values were slightly higher than that of S-flurbiprofen glucuronides (3. 9-18. 0 pg/mL).