Quantitative Analysis of Opiates in Urine Using RRHT LC/MS/MS. Application. Authors. Introduction. Abstract. Forensics

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Quantitative Analysis of piates in Urine Using RRHT LC/MS/MS Application Forensics Authors Sheher Mohsin Agilent Technologies, Inc. 10 N. Martingale Rd., Suite 550 Schaumburg, IL 60173 USA Yanan Yang Agilent Technologies, Inc. 5301 Stevens Creek Blvd. Santa Clara, CA 95051 USA Michael Zumwalt Agilent Technologies, Inc. 9780 S Meridian Blvd. Englewood, C 80112 USA Abstract An Agilent 6410 Triple Quadrupole Mass Spectrometer (QQQ) is used to analyze several opiates in urine. A simple isocratic liquid chromatography elution is carried out to detect all seven analytes and their respective internal standards in less than 3.5 minutes using Rapid Resolution High-Throughput liquid chromatography with a ZRBAX C18, 2.1 50 mm, 1.8-µm particle size column. Both quantifier and qualifier ions are monitored for each analyte, with the requirement that the qualifier/quantifier ion ratio be within ± 20% for confirming their presence in samples. Except for 6-acetylmorphine (6-MAM), all calibration standards are extracted in matrix and range from 1 to 150 pg/µl in urine. The range for 6-MAM is 0.067 to 10 pg/µl. Following extraction, which corresponds to a factor of 6.78 decrease in concentration, the injected concentrations range from 0.147 to 22.12 pg/µl, or 147 ppt to 22.12 ppb. For 6-MAM, this corresponds to 9.8 ppt to 1.5 ppb. All compounds show very good linearity (R 2 > 0.99). Introduction piates are drug compounds commonly used for sedation and pain relief and may be obtained both legally as prescription medication or illegally. Their abuse can often lead to addiction. For several reasons, including therapeutic drug monitoring, driving under the influence of drugs, and workplace drug testing, these compounds are commonly analyzed, particularly in urine due to ease of sample availability and volume. For testing in the area of forensics it is often necessary to provide additional confirmation of the presence of these compounds beyond their quantitative values exceeding defined cutoff values. The triple quadrupole mass spectrometer (QQQ) provides the most sensitive form of quantitation by acquiring the signal corresponding to the highest response product ion (quantifier) from the fragmentation of the analyte precursor ion. This transition is known as multiple reaction monitoring (MRM). However, by acquiring additional signal corresponding to the next highest product ion (qualifier), enough information may be considered available for confirmation, particularly if the ratio of signal between the two product ions is consistent between the calibration standards and the unknown samples. Using the QQQ to acquire MRM signals for both the quantifier and qualifier ions can result in both quantitation and confirmation simultaneously.

The Agilent MassHunter software includes userdefinable ion ratio confirmation in the quantitative analysis program as shown in Figure 1. The default tolerance for confirmation is ± 20% of the derived ion ratio, but this may be customized for the particular user. Additionally, up to four different product ions may be used as qualifiers. In this work, the default value of ± 20% is used, along with only one qualifier ion. Quantifier ± 20% tolerance verlay of qualifier and quantifier ions, normalized by peak area Figure 1. Qualifier/quantifier ion ratios for confirmation of oxymorphone. Several opiates in urine, including morphine, oxymorphone, hydromorphone, codeine, oxycodone, hydrocodone, and 6-acetylmorphine (6-MAM), a metabolite of heroin, are analyzed in this work. The corresponding structures are shown in Figure 2. A deuterated chemical analog for each compound is included to account for extraction efficiency and matrix interference. A qualifier ion for each internal standard is not necessary and is therefore not analyzed. 2

Morphine xymorphone Hydromorphone Codeine C 17 H 19 N 3 C 17 H 19 N 4 C 17 H 19 N 3 C 18 H 21 N 3 H H H N CH 3 H H N CH 3 H 3 C N H N CH 3 H 3 C H H H xycodone Hydrocodone 6-Acetylmorphine C 18 H 21 N 4 C 18 H 21 N 3 C 19 H 21 N 4 H 3 C H 3 C H H N CH 3 H N H 3 C N H 3 C CH 3 Figure 2. Structures of the opiates analyzed in this work. This work uses a gradient LC analysis consisting of only water and acetonitrile (no modifiers) to elute all analytes and corresponding internal standards in less than 3.5 min on a Rapid Resolution High- Throughput (RRHT) LC column with a 1.8-µm particle size. The complete cycle time from one injection to the next is about 8 minutes. The compounds are analyzed using an electrospray ionization source in positive ion mode. Parameters associated with this ion source, like drying gas, are standard for the LC flow rate of 0.4 ml/min, in which the samples are introduced into the mass spectrometer. Voltage settings for maximum ion transfer between the ion source and the mass analyzer components of the QQQ instrument are set using the autotune capability of the instrument to optimize signal intensity, resolution, and mass assignment across a wide mass range. ne parameter requiring optimization for each analyte is the fragmentor voltage, which is located in the ion transfer optics between the ion source and the mass analyzer. This optimization results in the maximum response of the precursor ion of interest incident upon the first quadrupole of the QQQ mass analyzer. The fragmentor voltage of 110 V worked best for all analytes. nce this is done, the optimal collision energy for fragmenting the precursor to form the highest possible response of a product ion is obtained. The mass spectrometer method development is now complete for the quantifier ion. Repeat optimizaton of the collision energy for the second mostabundant product ion and both MRM transitions are thus derived for one compound. Both steps in optimization may be carried out by flow injection analysis. 3

Experimental Sample Preparation Urine samples spiked with the opiate compounds were provided at the following labeled concentrations: 1, 5, 10, 50, 100, and 150 pg/µl, and a factor of 15 times lower for 6-MAM. These samples were then processed using the following procedure: 1. Start with 250-µL sample size 2. Add 500 µl sodium acetate buffer 3. Add 20 µl glucuronidase 4. Add 75 µl of internal standard mixture at 500 ng/ml concentration (de-ionized water) 5. Vortex 6. Incubate at 60 C for 20 minutes 7. Add 850 µl de-ionized water 8. Vortex and spin down 9. Place 200 µl of supernatant in sample vial All prepared samples provided by customer. This procedure dilutes the samples by a factor of 6.78 so that a 1 pg/µl concentration in urine has an actual concentration of 147 fg/µl for injection. Upon addition of internal standards and extraction, the starting concentrations in urine now correspond to the following concentrations for injection: 0.147, 0.737, 1.47, 7.37, 14.7, and 22.12 pg/µl. With a 5-µL injection volume (see LC Conditions), this range then corresponds to 0.737, 3.685, 7.35, 36.85, 73.5, and 110.6 pg on-column. For 6-MAM, all of these values are a factor of 15 lower. LC/MS Method Details LC Conditions Agilent 1200 Series binary pump, degasser, wellplate sampler, and thermostatted column compartment Column: Agilent ZRBAX SB-C18, 2.1 50 mm, 1.8-µm particle size (PN: 822700-902) Column temp: 50 C Mobile phase: A = water B = acetonitrile Flow rate: 0.4 ml/min Injection volume: 5 µl Gradient: Time (min) %B 0 2 4 40 Stop time: 6.1 min 4.1 90 Post time: 2.0 min 6 90 6.1 2 Needle wash (25:75 water/methanol) flush port 10 seconds MS Conditions Mode: Positive ESI using the Agilent G1948B ionization source Nebulizer: 60 psig Drying gas flow: 11 L/min Drying gas temp: 350 C V cap: 2000 V Resolution (FWHM): Q1 = 0.7; Q2 = 0.7 Dwell time for all MRM transitions = 50 msec Fragmentor voltage for all transitions = 110 V The MRM transitions for each compound are listed in Table 1 by retention time. Those product ions in parentheses are used as qualifiers. The retention times are included. Note that 6-MAM, or 6- monoacetylmorphine, is abbreviated as 6-MAM. Table 1. MRM Mode Parameters for piates Collision Retention Segment Compound Transition energy (V) time (min) 1 (0 min) D3-morphine 289.2 > 152.1 75 1.851 Morphine 286.2 > 152.1 (128.0) 75 (73) 1.862 D3-oxymorphone 305.2 > 230.1 33 2.138 xymorphone 302.2 > 227.1 (198.0) 33 (55) 2.146 D3-hydromorphone 289.2 > 157.1 50 2.379 Hydromorphone 286.2 > 185.0 (157.0) 33 (50) 2.385 2 (2.65 min) D3-codeine 303.2 > 152.0 75 2.908 Codeine 300.2 > 152.0 (115.0) 75 (85) 2.912 D3-oxycodone 319.2 > 244.1 30 3.109 xycodone 316.2 > 241.0 (256.0) 30 (27) 3.120 D6-6-MAM 334.2 > 165.1 40 3.161 6-MAM 328.2 > 165.0 (211.0) 40 (27) 3.168 D3-hydrocodone 303.2 > 199.1 28 3.245 Hydrocodone 300.2 > 199.0 (128.0) 28 (73) 3.249 4

Results and Discussion The calibration curves for all seven compounds are shown in Figures 3A through 3G, including expanded views of the lowest three levels. All calibration curves are generated using a linear fit, no inclusion of the origin, and a 1/x weighting. All curves have linearity coefficients of at least 0.99 and show good reproducibility and accuracy at the lowest levels. ne exception is 6-MAM, which only showed signal for two of the three injections at the lowest level (49 fg on-column). However, the corresponding concentration in urine is 0.067 pg/µl (0.067 ng/ml), which is much lower than the 10 ng/ml confirmatory cutoff level for workplace testing proposed by the U.S. Substance Abuse Mental Health Services Administration (SAMHSA). Morphine 1 1500 ppb in urine 0.74 110.6 pg on-column R 2 > 0.997 3 replicate injections at each level Figure 3A. Linearity of morphine in urine. Injection concentration range = 147 ppt 22 ppb. 5

xymorphone 1 150 ppb in urine 0.74 110.6 pg on-column R 2 > 0.997 3 replicate injections at each level Figure 3B. Linearity of oxymorphone in urine. Injection concentration range = 147 ppt 22 ppb. Hydromorphone 1 150 ppb in urine 0.74 110.6 pg on-column R 2 > 0.997 3 replicate injections at each level Figure 3C. Linearity of hydromorphone in urine. Injection concentration range = 147 ppt 22 ppb. 6

Codeine 1 150 ppb in urine 0.74 110.6 pg on-column R 2 > 0.997 3 replicate injections at each level Figure 3D. Linearity of codeine in urine. Injection concentration range = 147 ppt 22 ppb. xycodone 1 150 ppb in urine 0.74 110.6 pg on-column R 2 > 0.997 3 replicate injections at each level Figure 3E. Linearity of oxycodone in urine. Injection concentration range = 147 ppt 22 ppb. 7

6-MAM 0.067 10 ppb in urine 49 fg 7.5 pg on-column R 2 > 0.992 3 replicate injections at each level No signal for one injection at lowest level Figure 3F. Linearity of 6-MAM in urine. Injection concentration range = 9.8 ppt 1.5 ppb. Hydrocodone 1 150 ppb in urine 0.74 110.6 pg on-column R 2 > 0.998 3 replicate injections at each level Figure 3G. Linearity of hydrocodone in urine. Injection concentration range = 147 ppt 22 ppb. 8

Confirmation is carried out by examining the qualifier/quantifier ion ratio and making sure it stays within ± 20% of the determined value for each analyte. For example, after optimizing the MRM transitions for both product ions of morphine, it is automatically determined by the MassHunter Quantitative Analysis that the ratio of the qualifier peak to that of the quantifier should be 0.7%, or 70%. Applying a ± 20% tolerance to this ratio means that all calibration standards and samples analyzed in this batch should have a ratio of 0.56 to 0.84 in order to confirm the presence of morphine. The lowest calibration levels that consistently satisfy the confirmation requirement for each analyte are shown in Figures 4A through 4G. Note that with the exception of oxycodone and 6-MAM, the confirmation ion ratio for all analytes is satisfied at the corresponding lowest calibration levels of 1 pg/µl in urine. For oxycodone and 6-MAM, the lowest levels are 5 and 0.3 pg/µl, respectively. Limits of detection (shown in Figures 5A through 5G) are also determined for this work using the quantifier ion of each analyte and based on a visual determination of peak-to-peak signal-tonoise ratio of at least 3:1 and a peak area %RSD (percent relative standard deviation) of 30 or less. The results for all analytes except oxycodone and 6-MAM are based on eight 1-µL injections at 147 fg on-column each. These correspond to original concentrations in urine of 1 pg/µl. For oxycodone, the LD is determined from the triplicate 5-µL injections of the calibration level corresponding to 1 pg/µl (see Figure 5E). Like oxycodone, the LD of 6-MAM is seen at a 5-µL injection, but of the 0.067 pg/µl level. However, only two of the three injections had signal so an area %RSD was not calculated. These values are further tabulated in Table 2. 0.74 fg on-column Figure 4A. Confirmation of morphine at 1 pg/µl (147 fg/µl). 9

0.74 fg on-column Figure 4B. Confirmation of oxymorphone at 1 pg/µl (147 fg/µl). 0.74 fg on-column Figure 4C. Confirmation of hydromorphone at 1 pg/µl (147 fg/µl). 10

0.74 fg on-column Figure 4D. Confirmation of codeine at 1 pg/µl (147 fg/µl). 3.7 pg on-column Figure 4E. Confirmation of oxycodone at 5 pg/µl (737 fg/µl). 11

245 fg on-column Figure 4F. Confirmation of 6-MAM at 0.3 pg/µl (49 fg/µl). 0.74 pg on-column Figure 4G. Confirmation of hydrocodone at 1 pg/µl (147 fg/µl). 12

Area RSD = 30% n = 8 Area RSD = 26% n = 8 Figure 5A. LD of morphine at 147 fg on-column. Figure 5B. LD of oxymorphone at 147 fg on-column. Area RSD = 25% n = 8 Area RSD = 28% n = 8 Figure 5C. LD of hydromorphone at 147 fg on-column. Figure 5D. LD of codeine at 147 fg on-column. 13

Area RSD = 17% n = 3 Area RSD = N/A n = 2 Figure 5E. LD of oxycodone at 737 fg on-column. Figure 5F. LD of 6-MAM at 49 fg on-column. Peak area %RSD not applicable because only two of three injections contained signal. Area RSD = 18% n = 8 Table 2. Determined Limits of Detection (LDs) in Urine for Each Analyte Analyte LD (fg on-colunn) Morphine 147 xymorphone 147 Hydromorphone 147 Codeine 147 xycodone 737 6-MAM 49 Hydrocodone 147 Figure 5G. LD of hydrocodone at 147 fg on-column. 14

Conclusions piates are successfully analyzed in the presence of urine. Good linearity (R 2 > 0.99) is obtained for all compounds over two orders magnitude in concentration range, which is 1 to 150 ppb for all analytes except 6-MAM; for 6-MAM this range is 0.067 to 10 ppb. After processing the samples and considering the 5-µL injection volume, this range corresponds to 0.74 to 110.6 pg on-column (49 fg to 7.5 pg for 6-MAM). The calibration curve fitting is carried out with no inclusion of the origin, a linear fit, and a 1/x weighting. At the lowest levels very good reproducibility and accuracy is demonstrated. Limits of detection are less than 1 pg oncolumn for all analytes. The Agilent 6410 QQQ is an excellent instrument for sensitive quantitation in a relatively dirty matrix. For More Information For more information on our products and services, visit our Web site at www.agilent.com/chem. For more details concerning this application, please contact Michael Zumwalt at Agilent Technologies, Inc. 15

www.agilent.com/chem Agilent shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. Information, descriptions, and specifications in this publication are subject to change without notice. Agilent Technologies, Inc. 2007 Printed in the USA August 8, 2007 5989-7213EN