Application Note: 346 MS/MS as an LC Detector for the Screening of Drugs and Their Metabolites in Race Horse Urine Gargi Choudhary and Diane Cho, Thermo Fisher Scientific, San Jose, CA Wayne Skinner and Scott Stanley, University of California Davis Key Words LCQ Advantage MAX Surveyor Data Dependent Drug Screening Metabolite ID Toxicology Introduction is a tricyclic antidepressant drug that is not a Drug Enforcement Administration controlled substance but has been classified by the Association of Racing Commissioners International Inc. as a class two drug in horses. is a major metabolite of imipramine. These two analytes were analyzed on-line by LC PDA MS/MS from extracts of horse urine. The urine sample was first treated with β-glucuronidase to hydrolyze glucuronide conjugates of imipramine and desipramine. This was followed by solid phase extraction. The concentration of imipramine and desipramine in the sample was determined by the internal standard method using the peak area ratio and linear regression analysis. This application note presents a rapid method for quantitation of imipramine and desipramine in horse urine. It illustrates the advantages of MS/MS detection in terms of specificity, sensitivity and unambiguous identification, for the analysis of drugs and their metabolites. Goal 1) Develop a rapid method to identify and quantitate tricyclic antidepressant imipramine and its major metabolite desipramine in horse urine. 2) Demonstrate the advantages of using MS/MS to identify and confirm the detection of imipramine and its metabolites. 3) Determine presence and structure of minor metabolites using Data Dependent LC-MS/MS analysis. Experimental Conditions HPLC LC system: Thermo Scientific Surveyor MS Pump, Surveyor Autosampler and Surveyor PDA Detector Mobile phase: A: water containing.2% formic acid B: Acetonitrile containing.2% formic acid Column: 5 2.1 mm, 5 µm Thermo Scientific Hypersil C18 Column Injection volume: 1 µl Flow rate: 2 µl/min Gradient: % A %B 98 2.2 98 2 8 25 75 9 1 9 1 1 9 1.1 98 2 15 98 2
Mass Spectrometer Mass spectrometer: Thermo Scientific LCQ Advantage MAX Ionization mode: Positive electrospray ionization (ESI) Capillary temperature: 275 C Spray voltage: 4.5 kv Sheath gas: 3 units Sweep gas: 8 units Quantifying Isolation Collision Scan MS/MS Analyte MH + Width Energy % Range Product Ions 281.2 1.5 3 75-285 86 267.2 1.5 3 7-29 236 (internal standard) 315.2 4 35 85-32 27 Table 1: MS parameters for imipramine, desipramine, and clomipramine (internal standard) Standards Calibration standards were prepared as follows: Volume of Volume of and Equivalent to Equivalent to working Calibration working standard standard in the urine in the urine level solution (µl) solution (µl) (ng/ml) (ng/ml) C1 1:1 Dilution of C2 1 15.6 5 C2 1:1 Dilution of C3 1 31.3 5 C3 1:1 Dilution of C2 1 62.5 5 C4 1:1 Dilution of C2 1 125 5 C5 1:1 Dilution of C2 1 25 5 C6 1:1 Dilution of C2 1 5 5 C7 1:1 Dilution of C2 1 5 C8 1:1 Dilution of C2 1 2 5 C9 1:1 Dilution of C2 1 4 5 C1 16 1 8 5, desipramine and clomipramine working standard solutions were 5 ng/ml Results and Discussions LC-UV-MS/MS analysis of imipramine and desipramine Figures 1 and 2 show the analysis of tricyclic antidepressant imipramine, its major metabolite desipramine, and the internal standard clomipramine by LC with MS/MS and UV detection, respectively. Figure 1 shows base peak and extracted ion chromatograms for the three analytes along with MS and MS/MS spectra. The MS and MS/MS spectra help in unambiguous identification of these analytes and represent the high specificity that can be obtained from such an analysis. Further, the MS/MS spectra can be stored in a library and used for rapid confirmation of the drug and its metabolite. Figure 2 shows total spectra obtained from a PDA detector as well as UV trace at 254 nm and 28 nm. The position of elution of the three compounds had to be determined by sequential injections of individual analytes. As illustrated in Figure 2, the UV spectra for these compounds appear almost identical, making their unambiguous identification difficult. Samples and Internal Standard was administered to the horse and a urine sample drawn after, 2, 4, 8 and 24 hours, post dose. One ml of the urine sample was spiked with 1 µl of 5 ng/µl clomipramine internal standard. Sample Preparation The calibration standard and urine samples were treated with β-glucuronidase to hydrolyze glucuronide conjugates of desipramine and imipramine, followed by solid phase extraction. Page 2 of 8
9.12 11.51 Base peak 9.55 NL: 1.74E6 9.9 NL: 8.23E5 m/z=266.5-267.5 9.53 NL: 7.63E5 m/z=28.5-281.5 11.51 NL: 9.22E5 m/z=314.5-315.5 5. 5.5 6. 6.5 7. 7.5 8. 8.5 9. 9.5 1. 1.5 11. 11.5 12. 12.5 T: + c ESI Full ms [15.-32.] 267. 281. MS Spectra 216.9 162.9 162.9 216.8 227.6 162.9 216.9 236. 278.9 15 2 25 3 15 2 25 3 15 2 25 m/z m/z m/z 3 267.1@35. 281.3@35. 315.3@35. [6.-545.] [65.-575.] [75.-645.] 236. 85.9 27. 3 5 m/z 236. MS/MS Spectra 3 5 m/z Figure 1: LC-MS/MS analysis of imipramine, desipramine and clomipramine (internal standard) 242.1 3 5 m/z uau 2 Total Scan NL: 2.1E4 Total Scan PDA uau Relative Absorbance uau 2 8 6 4 UV @ 254 nm 6 9.2 UV @ 28 nm 9.45 4 2 5. 7. 9. NL: 2.754E4 UV @ 254 nm NL: 6.75E3 UV @ 28 nm 235. 235. 235. UV 8 6 4 9.3 9.46 8 6 4 11.43 11.43 11. 12. 12.5 Spectra 2 2 3 4 5 6 wavelength (nm) 2 2 3 4 5 6 wavelength (nm) 2 2 3 4 5 6 wavelength (nm) Figure 2: LC-UV analysis of imipramine, desipramine and clomipramine (internal standard) Page 3 of 8
Figure 3 shows chromatograms obtained for the analysis of imipramine, desipramine and clomipramine (IS) with MS and UV detection at levels of 5 and.5 ng on-column. At.5 ng on-column, both imipramine and desipramine could be easily identified when MS was used as a detector whereas these analytes were hardly visible in the UV trace. The concentration of clomipramine is the same at both these levels. This illustrates the excellent sensitivity that can be obtained during analysis by LC-MS/MS. Quantitation of imipramine and desipramine in horse urine Figures 4 and 5 show calibration curves obtained for imipramine and its major metabolite desipramine in horse urine with clomipramine used as an internal standard. The coefficient of correlation is.9896 for calibration curve of imipramine and.9836 for the calibration curve of desipramine. The % CV values are less than 7% for the imipramine calibration curve and 15% for the 9 8 7 6 5 4 3 2 1 9 8 7 6 5 4 3 2 1 MS Detection 8.45 8.78 1.26 1.25 4 5 6 7 8 9 1 11 12 NL: 2.15E6 m/z=266.7-267.7+28.7-281.7+314.7-315.7 F: + c ESI Full ms [15.-32.] NL: 1.76E6 m/z=266.7-267.7+28.7-281.7+314.7-315.7 F: + c ESI Full ms [15.-32.] uau uau 14 12 8 6 5 ng on-column 2 8 6 4.5 ng on-column UV Detection 7.13 7.12 7.77 8.36 8.69 / 7.76??? 1.16 1.15 11.1 4 5 6 7 8 9 1 11 12 NL: 1.51 E4 UV @ 28 nm NL: 1.27 E4 UV @ 28 nm Figure 3: Comparison of MS and UV detection at two different concentrations Page 4 of 8
5 Y =.477544*X R^2 =.9896 W: Equal Area Ratio 4 3 2 1 N N CH3 CH3 Calibration level 2 4 6 8 pg (on-column) C1 C2 C3 C4 C5 C6 C7 Amount on column (pg) 15.6 31.3 62.5 125 25 5 % CV 4.25 1.25 2.28 7.34 5.32 3.65 4. Figure 4: Calibration curve for imipramine in horse urine Y =.164932*X R^2 =.9835 W: Equal 1.5 N Area Ratio 1. NH CH3 Calibration level C3 C4 Amount on column (pg) 62.5 125 % CV 14.96 14.3.5 C5 C6 25 5 11.24 4.73 C7 4.2. 2 4 6 8 pg (on-column) Figure 5: Calibration curve for desipramine in horse urine Page 5 of 8
desipramine calibration curve. Figure 6 shows analysis of imipramine and desipramine in horse urine sample drawn two hours post-administration of the drug. The amount of imipramine and its major metabolite desipramine was determined using the calibration curves shown in Figures 4 and 5. Table 2 shows the amount of these two analytes as determined in horse urine. For the sample drawn two hours post-administration of the drug, the amount of imipramine and desipramine was determined to be 28 and 1567 ng/ml, respectively. The amount of desipramine determined at this time is above the upper limit of quantitation for the calibration curve shown in Figure 5. Time (hr) (ng/ml) (ng/ml) + 17.56 2.85* 2 28.12 1567.16** 4 4.25* 189.6 8 6.75* 96.56 24 6.11* 13.11* Identification of metabolites of imipramine A urine sample from the race horse obtained two hours after administration of the drug was also analyzed by Data Dependent LC-MS/MS, with MS/MS on the top two most intense ions to determine the presence of other metabolites. Figure 7 shows the workflow for such an analysis. The extracted ion chromatograms in Figure 8 show the presence of four additional metabolites: desmethyl desipramine, OH desipramine, OH-imipramine, and N-Oxide of imipramine, as well as their MS/MS fragmentation pattern. As indicated by the two peaks in the extracted ion chromatogram for m/z 297.2, imipramine is metabolized to two metabolites that have the same m/z. In this case, the MS/MS fragmentation pattern enables unambiguous distinction between the two metabolites. Table 2: Determination of imipramine and desipramine in horse urine for samples drawn at different times post injection of the drug (*below lower limit of quantitation, **above upper limit of quantitation) Relative Abundance Relative Abundance 8. 47 8. 47 8. 88 1. 46 1. 46 4 5 6 7 8 9 1 11 12 13 14 T: + c ESI Full ms2 281.2@3. [75.-285.] 86. 8 236.1 6 4 2 Base Peak 26. T: + c ESI Full ms2 267.2@3. [75.-27.] 236. NL: 1.3E5 Base Peak MS NL: 5.95E3 m/z=85.5-86.5 NL: 1.75E5 m/z=235.5-236.5 NL: 4.21E4 m/z=269.5-27.5 T: + c ESI Full ms2 315.2@35. [85.-32.] 27. 15 2 25 15 2 25 15 2 25 3 m/z m/z m/z Figure 6: Analysis of imipramine and desipramine in horse urine for sample drawn two hour post-administration of drug Page 6 of 8
Optimize MS parameters by tuning Setup LC Parameters Mobile phase, column, gradient Full-scan LC-MS/MS analysis of the sample with MS/MS on the top n (in this case top 2) peaks Data analysis using Metabolite ID Figure 7: Workflow for the identification of imipramine and its metabolite in horse urine Relative Abundance Relative Abundance 8 6 Demethyl- OH- 6.42 6.52 6.56 OH- 6.52 6.56 N-oxide of 1 2 3 4 5 6 7 8 9 1 11 12 13 14 236. 236. Demethyl- 8.1 8.36 252. OH- 4 28.1 252. 2 223.9 28. 86. 279.1 196.2 196. 2 4 2 4 2 4 2 4 6 2 4 6 m/z m/z m/z m/z m/z 268.7@35. [6.-54] 253.7@35. [55.-52] 283.12@35. [65.-58] 279. OH- 297.15@35. [7.-65] 85.9 NL: 3.5E6 m/z=266.7-267.7 NL: 1.43E6 m/z=252.5-253.5 NL: 1.13E7 m/z=282.7-283.7 NL: 7.98E6 m/z=296.7-297.7 NL: 7.98E6 m/z=296.7-297.7 N-oxide of 297.12@35. [7.-65] Figure 8: Data Dependent LC-MS/MS analysis of metabolites of imipramine Page 7 of 8
Conclusions Full scan MS/MS analysis using a Thermo Scientific LCQ Advantage MAX ion trap mass spectrometer provides the selectivity and sensitivity necessary to support ADME/Tox studies of imipramine in horse urine. Analysis of drugs and their metabolites in complex biological samples using MS/MS detection enables unambiguous identification of these analytes. Data Dependent LC-MS/MS analysis facilitates presence and structural determination of several co-eluting minor metabolites. MS/MS information is invaluable in the identification of metabolites with the same m/z (e.g., OH-imipramine and N-oxide of imipramine). Acknowledgements The authors wish to thank Marta Kozak for sample analyses and Julian Phillips for presenting this project at the HPLC 24 conference. In addition to these offices, Thermo Fisher Scientific maintains a network of representative organizations throughout the world. Africa +43 1 333 534 127 Australia +61 2 8844 95 Austria +43 1 333 534 Belgium +32 2 482 3 3 Canada +1 8 53 8447 China +86 1 585 3588 Denmark +45 7 23 62 6 Europe-Other +43 1 333 534 127 France +33 1 6 92 48 Germany +49 613 48 114 India +91 22 6742 9434 Italy +39 2 95 591 Japan +81 45 453 9 Latin America +1 68 276 5659 Middle East +43 1 333 534 127 Netherlands +31 76 587 98 88 South Africa +27 11 57 184 Spain +34 914 845 965 Sweden/Norway/ Finland +46 8 556 468 Switzerland +41 61 48784 UK +44 1442 233555 USA +1 8 532 4752 www.thermo.com Legal Notices 216 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific Inc. and its subsidiaries. This information is presented as an example of the capabilities of Thermo Fisher Scientific Inc. products. It is not intended to encourage use of these products in any manners that might infringe the intellectual property rights of others. Specifications, terms and pricing are subject to change. Not all products are available in all countries. Please consult your local sales representative for details. View additional Thermo Scientific LC/MS application notes at: www.thermo.com/appnotes AN62533_E 6/16S Part of Thermo Fisher Scientific