ABSTRACT The traditional study of in vivo drug metabolism in plasma or urine samples is often complicated by the presence of many endogenous compounds. Several mass spectrometric techniques are often applied in drug metabolism studies. Conjugation reactions, particularly glucuronidation, can be studied using either the neutral loss or precursor ion experiment, however the experiments are not usually done at the same time. Using a hybrid quadrupole/time of flight instrument, a new method of performing the neutral loss and precursor ion scan experiments simultaneously has been devised. Using this novel approach, which is more sensitive and selective than the corresponding triple quadrupole experiments, several Phase 1 and Phase 2 metabolites of diphenhydramine were identified from a human urine sample collected 4 hours after drug administration. Accurate mass measurements were made in the same acquisition, and elemental compositions of the found metabolites were assigned to within 5 ppm. Diphenhydramine was extensively metabolized to form a number of excreted metabolites, including N-demethylation, aryl, and N-hydroxy metabolites. Glucuronide conjugation was observed for several of the hydrox-metabolites as well as the N-glucuronide. RAPID, SELECTIVE SCREENING F URINE SAMPLES FR GLUCURNIDES BY LC/MS/MS Andrew G. Baker*, Nicholas J. Ellor, Jennifer L. Jones; Waters Corporation, MS Technology Center, Cummings Center, Suite 47N, Beverly, MA 1915 INTRDUCTIN Mass spectrometry is a well-established technique used in many ways throughout the drug discovery and development process. Profiling both in vitro samples for initial metabolic information and in vivo samples such as plasma, bile, or urine for a more complete description of drug metabolism is one such area. As the pharmaceutical life cycle evolves, metabolism studies are often brought into the discovery phase to reject compounds with poor metabolic profiles or toxicity issues earlier in the timeline. Synthesis of radioactive analogues for metabolism studies is not feasible, thus other, more selective techniques must be used. Conjugation reactions such as glucuronidation or sulfation serve to increase the polarity of a drug or metabolite, making excretion more likely. These Phase 2 metabolites are often studied using the classic triple quadrupole neutral loss experiment. This experiment, while well suited for selectively detecting conjugated metabolites from complex samples such as urine or bile cannot be used to assay several metabolic processes at once, as the quadrupoles are scanned with a mass offset corresponding to the conjugate. To determine another conjugation, either a loss in duty cycle from alternating scans with different mass offsets or another LC/MS acquisition is required. Two novel experiments using a hybrid quadrupole- time of flight Q-Tof instrument have been devised to overcome this limitation in duty cycle. 1 As this experiment is performed using the Q-Tof, the resulting accurate mass MS/MS spectrum is particularly useful for structural elucidation. Diphenhydramine is a well characterized Histamine H1 receptor antagonist. The major urinary metabolites include a N + glucuronide, N-xide, as well as several minor metabolites. 2,3,4 This model system was used to demonstrate the application of these two novel Q-Tof experiments.
EXPERIMENTAL Urine was collected immediately before and 4 hours after administration of a single 25 mg dose of generic diphenhydramine and frozen until analysis. Urine samples were diluted 1:5 with Milli-Q water prior to analysis. No other sample pretreatment was done. LC Conditions: A Waters 2795 XC Separations Module equipped with a Waters Symmetry C 18 column (2.1 x 15 mm) and 2996 photodiode array detector was used for the chromatographic separation. Mobile Phases: A=.5 Aqueous Trifluoroacetic Acid B= 95 Acetonitrile: 5 Water:.5 Trifluoroacetic Acid Gradient: 5 to 5 B in 7.5 Minutes Ramp to 95 B in.5 Minute Hold 1 Minute Return to Initial Conditions Flow Rate:.2 ml/min Mass Spectrometer: A Waters Q-Tof Ultima API-US mass spectrometer equipped with LockSpray was operated in positive ion electrospray mode. Prior to use, the instrument was tuned to greater than 1, resolution (FWHM) and calibrated using polyalanine. Leucine enkephalin was infused through the reference channel for on-line acquisition of accurate mass measurements. Mass Accuracy Table Metabolite Retention Theoretical m/z Experimental m/z Mass Accuracy (ppm) Mass Accuracy (mda) Diphenhydramine HydroxyGlucuronide 1.5 448.1971 448.1968 -.8 -.4 Diphenhydramine HydroxyGlucuronide 11 448.1971 448.1985 3.1 1.4 Diphenhydramine HydroxyGlucuronide 12.1 448.1971 448.1959-2.7-1.2 Diphenhydramine N-Glucuronide 14.1 432.222 432.25-3.9-1.7 Diphenhydramine 15.2 256.171 256.178 2.5.6 Diphenhydramine N-xide 15.9 272.1651 272.1638-4.5-1.2 Mean Error -1.1 -.4 Standard Deviation 3.2 1.2
Exact Neutral Loss Mode The offset voltage on the collision cell is modulated between low (5 ev) and high (15 ev) voltages on alternate acquisitions. Ions are selected for subsequent MS/MS acquisition based on the presence of a defined neutral loss between pairs of ions in the low and high collision energy survey acquisitions. Because of the high resolution and high mass accuracy of the TF mass analyzer, very stringent criteria (1 ppm mass accuracy) can be used to select ions for the MS/MS acquisition. 42 42 9.93 9.95 9.97 432 9.5 9.6 9.7 9.8 9.9 1. 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 1.27 464 MS/MS for Species with Specified Neutral Loss High Energy Survey Scan 1.48 1.72 Low Energy Survey Scan 1.5 1.78 85. 13.1 256.2 256.2 271.2 286.2 MS/MS Acquisition of m/z 432 Triggered by Exact Neutral Loss Low CE Acquisition High CE Acquisition 6 8 12 14 16 18 2 22 24 26 28 3 32 34 36 38 4 42 44 46 48 5 52 432.3 432.2 m/z 9.97 432 MS/MS for Species with Specified Neutral Loss 9.95 Diphenhydramine N-Glucuronide 8.13 9.95 TIC 1.97 1.5 11.68 1.81 2.24 6.84 7.52 8.39 8.99 2 1. 2. 3. 4. 5. 6. 7. 8. 9. 1. 11. 12. Fast separation of Diphenhydramine and metabolites in Urine. Top trace is specific trace for Exact Neutral Loss of Glucuronide 1.49 Hydroxy-Glucuronides 12.1 14.6 N-Glucuronide 15.18 Diphenhydramine 14.11 15.92 N-xide 2.25 TIC 9.74 1.51 13.42 14.6 14.92 15.92 2. 4. 6. 8. 1. 12. 14. 16. 18. Extracted Ion Current for Diphenhydramine Metabolites in Urine
H 432.235 H H N + H 286.232 454.216 5 15 2 25 3 35 4 45 5 55 6 65 7 75 8 85 9 95 m/z Mass Calc. Mass mda PPM DBE Score Formula 432.235 432.222 1.3 2.9 9.5 1 C23 H3 N 7 Spectrum and elemental composition report for Diphenhydramine N-Glucuronide peak at 9.97 minutes 167.865 H H m/z 256 H H N + 256.1711 432.241 m/z 167 6 8 12 14 16 18 2 22 24 26 28 3 32 34 36 38 4 42 44 46 m/z Elemental Composition Report Mass RA Calc. Mass mda PPM DBE Score Formula 167.865. 167.861.4 2.5 8.5 1 C13 H11 256.1711 3.56 256.171 1. 3.7 7.5 1 C17 H22 N 432.241 2.37 432.222 1.9 4.3 9.5 1 C23 H3 N 7 MS/MS Spectrum and Elemental Composition report for Diphenhydramine N-Glucuronide peak at 9.97 minutes MetaboLynx Processing of Expected and Unexpected Metabolites from Diphenhydramine
Precursor Ion Discovery Mode The Q-Tof is operated in the normal fashion, however the offset voltage on the collision cell is modulated between low (5 ev) and high (15 ev) voltages on alternate acquisitions. nly after a fragment ion is found in the high energy survey scan will ions be selected for MS/MS from the low energy survey scan. Because of the high resolution and high mass accuracy of the TF mass analyzer, very stringent criteria (1 ppm mass accuracy) are used to identify fragment ions that trigger the MS/MS acquisition. 1.72 1.74 1.98 11. 11.6 272 MS/MS Acquisition Triggered by Presence of Defined Fragment Ion.6 1.7 1.8 1.9 11. 11.1 11.2 11.3 11.4 11.5 11.21 32 11.51 314 High Energy Survey Scan Low Energy Survey Scan MS/MS Acquisition of m/z 272 Triggered by Presence of Defined Fragment Ion High CE Acquisition Low CE Acquisition 5 6 7 8 9 11 12 13 14 15 16 17 18 19 2 21 22 23 24 25 26 27 28 29 3 31 32 33 m/z 272.2 272.2 7.98 265 1.2 432 MS/MS Acquisition 11.6 272 11.65 358 Diphenhydramine N-xide 11. 9.96 Diphenhydramine Glucuronide TIC 1.81 2.31 6.46 7.5 7.48 8.9 9.11 9.96 11. 1.44 1.74 11.63 1 1. 2. 3. 4. 5. 6. 7. 8. 9. 1. 11. 12. Fast Separation of Diphenhydramine Metabolites from urine using Precursor Ion Discovery Acquisition 272.1643 N m/z 14 15 16 17 18 19 2 21 22 23 24 25 26 27 28 29 Mass Calc. Mass mda PPM DBE Score Formula 272.1643 272.1651 -.8-2.8 7.5 1 C17 H22 N 2 Spectrum and elemental composition report for Diphenhydramine N-xide Metabolite peak at 11. minutes
167.864 m/z167 N m/z 6 8 12 14 16 18 2 22 24 26 28 3 Mass Calc. Mass mda PPM DBE Score Formula 167.864 167.861.3 1.9 8.5 1 C13 H11 MS/MS Spectrum and elemental composition report for Diphenhydramine N-xide peak at 11. minutes Conclusions Q-Tof accurate mass MS and MS/MS are useful for metabolite structural elucidation Major metabolites of Diphenhydramine-- Diphenhydramine N-Glucuronide and Diphenhydramine N-xide identified and characterized Novel Precursor Ion Discovery DDA mode with concominant search for neutral losses increases the duty cycle over the classic triple-quadrupole experiments. Stringent mass accuracy criteria (1 ppm) for identifying fragment ions or neutral losses enables higher quality results Specificity of ENL maintained under fast gradient conditions References 1. Langridge, J.I., Hoyes, J.B., Bateman, R.H., Millar, A.L., Carruthers, R., Jones, C., and Jensen,.N., Poster at 49th ASMS 21. 2. Sharma, A. and Hamelin, B.A. Curr. Drug Metab. 23, 4, 15-129. 3. Luo, H., Hawes, E.M., McKay, G., Korchinski, E.D., and Midha, K.K., Xenobiotica 1991, 21, 1281-1288 4. Drach, J.C., and Howell, J.P. Biochem. Pharmacol. 1968, 17, 2125-2136. WATERS CRPRATIN 34 Maple St. Milford, MA 1757 U.S.A. T: 58 478 2 F: 58 872 199 www.waters.com Waters, Q-Tof, Q-Tof Ultima, Symmetry and LockSpray are trademarks of Waters Corporation. All other trademarks are the property of their respective owners. 23 Waters Corporation Produced in the U.S.A. ctober 23 72774EN LW-PDF