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Pain Management Poster
2012-05-17T10:25:32-04:00
2012-05-17T10:25:32-04:00
2012-05-17T10:25:32-04:00
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Q
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q
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h
f
Q
Q
q
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h
-3.27 -0.828 m
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h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
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1.036 -0.84 l
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0 -5.457 l
h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
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0 0 m
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2.822 -4.26 l
2.844 -4.26 l
4.387 0 l
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h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
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316.79 1364.918 -0.759 19.957 re
B
Q
q
1.4634247 0 0 1.4942627 0 0 cm
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f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
0 0 0 0 K
1.459 w 4 M
/GS2 gs
q 1 0 0 1 328.5984 1382.7787 cm
0 0 m
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h
S
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
q 1 0 0 1 356.6655 1385.0527 cm
0 0 m
23.496 -17.557 l
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24.254 -0.178 l
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0.758 -1.885 l
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0 -20.135 l
h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
0 0 0 0 K
1.459 w 4 M
/GS2 gs
q 1 0 0 1 356.6655 1385.0527 cm
0 0 m
23.496 -17.557 l
23.496 -0.178 l
24.254 -0.178 l
24.254 -19.442 l
0.758 -1.885 l
0.758 -20.135 l
0 -20.135 l
0 0 l
h
S
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
0 0 0 0 K
1.459 w 4 M
/GS2 gs
387.862 1364.918 -0.758 19.957 re
B
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
q 1 0 0 1 418.2005 1367.6406 cm
0 0 m
-2.453 -2.155 -6.64 -3.5 -10.91 -3.5 c
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1.776 1.824 1.117 0.988 0 0 c
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
0 0 0 0 K
1.459 w 4 M
/GS2 gs
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1.496 11.459 l
0.859 12.386 0.36 12.926 -0.339 13.552 c
-1.356 14.422 -2.971 15.318 -4.587 15.886 c
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2.395 3.052 l
1.776 1.824 1.117 0.988 0 0 c
h
S
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
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h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
0 0 0 0 K
1.459 w 4 M
/GS2 gs
q 1 0 0 1 442.3065 1383.7717 cm
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0 1.105 l
0 0 l
h
S
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
q 1 0 0 1 254.6065 1364.4727 cm
0 0 m
15.196 -0.069 27.493 -11.451 27.493 -25.485 c
27.493 -11.408 39.862 0.004 55.122 0.004 c
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55.213 0.006 55.166 0.002 55.122 0.002 c
39.862 0.002 27.493 11.414 27.493 25.49 c
27.493 11.457 15.196 0.074 0 0.006 c
h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/CS0 cs 1 scn
/GS2 gs
q 1 0 0 1 265.5685 1364.4746 cm
0 0 m
9.167 -0.041 16.585 -6.908 16.585 -15.373 c
16.585 -6.883 24.046 0.002 33.251 0.002 c
33.279 0.002 33.306 0 33.334 0 c
33.334 0.002 l
33.251 0.002 l
24.046 0.002 16.585 6.884 16.585 15.375 c
16.585 6.91 9.167 0.045 0 0.002 c
h
f
Q
Q
q
1.4634247 0 0 1.4942627 0 0 cm
/GS2 gs
q 1 0 0 1 306.0945 1385.2966 cm
0 0 m
-1.099 1.062 -5.472 -1.309 -11.056 -5.713 c
-15.671 -9.488 l
-10.085 -5.084 -7.624 -3.855 -6.525 -4.918 c
-4.886 -6.502 -11.157 -15.133 -20.531 -24.191 c
-22.897 -26.477 -25.234 -28.57 -27.433 -30.4 c
-23.743 -27.971 -18.937 -24.037 -14.007 -19.273 c
-4.632 -10.213 1.639 -1.584 0 0 c
f
Q
Q
Q
0 0.5 1 0 k
275.41 2193.698 1510.708 -87.763 re
f*
BT
0 0 0 1 k
/TT0 1 Tf
67.6207 0 0 55.8 850.8916 2125.2437 Tm
(Introduction)Tj
ET
0 0.5 1 0 k
273.614 1689.135 1510.709 -87.763 re
f*
BT
0 0 0 1 k
/TT0 1 Tf
81.8759 0 0 55.8 885.9116 1620.1899 Tm
(Method)Tj
30 0 0 30 285.7446 2039.7983 Tm
(LC-MS/MS has emerged as a reliable method to perform both screening and \
confirmation of the presence of )Tj
0 -1.2 TD
(drugs \(of abuse or for pain management\). Routine testing of urine or o\
ther biological specimens for prescribed )Tj
T*
(pain medication is critical to monitor compliance and prevent misuse or \
abuse. Urine is used for analysis be)Tj
47.467 0 Td
(-)Tj
-47.467 -1.2 Td
[(cause it can be collected easily)73(. However)55(, patient urine composition is highly variable and dependent their diet,\
)]TJ
T*
[(health and lifestyle. )17(These variations in the urine matrix can have an adverse impact on the c\
hromatographic )]TJ
T*
[(separation and LC-MS/MS signal. )17(The present study demonstrates that a simple dilute and shoot method )]TJ
T*
(coupled with a highly sensitive LCMS system is feasible to eliminate a t\
ypical sample clean-up step without )Tj
T*
[(compromising quantitation quality)72(.)]TJ
ET
0 0.5 1 0 k
3617.77 649.017 1377.199 -87.762 re
f*
BT
0 0 0 1 k
/TT0 1 Tf
83.4216 0 0 55.8 4131.3652 588.8262 Tm
(Conclusion)Tj
ET
q
4531.851 81.756 m
4316.124 81.756 4105.363 120.488 3889.64 120.488 c
3889.64 120.488 l
3673.912 120.488 3464.981 87.301 3249.252 87.301 c
3249.252 87.301 l
3033.528 87.301 2811.004 120.488 2595.28 120.488 c
2595.28 120.488 l
2379.553 120.488 2161.114 81.756 1945.388 81.756 c
1945.388 81.756 l
1729.662 81.756 1516.643 120.488 1300.918 120.488 c
1300.918 120.488 l
1085.192 120.488 868.49 84.528 652.765 84.528 c
652.765 84.528 l
437.038 84.528 222.286 120.488 6.56 120.488 c
6.56 120.488 l
6.56 0.912 l
653.741 0.912 l
1300.918 0.912 l
1948.102 0.912 l
2595.28 0.912 l
3242.456 0.912 l
3889.64 0.912 l
4536.815 0.912 l
5183.999 0.912 l
5183.999 120.488 l
4968.271 120.488 4747.58 81.756 4531.851 81.756 c
W n
q
0 g
1 0 0 -1 0 0 cm
BX /Sh0 sh EX Q
Q
q
4528.255 93.532 m
4312.535 93.532 4105.324 129.57 3889.606 129.57 c
3889.606 129.57 l
3673.886 129.57 3461.816 93.532 3246.099 93.532 c
3246.099 93.532 l
3030.378 93.532 2811.004 129.57 2595.283 129.57 c
2595.283 129.57 l
2379.563 129.57 2163.842 90.76 1948.119 90.76 c
1948.119 90.76 l
1732.404 90.76 1516.684 129.57 1300.958 129.57 c
1300.958 129.57 l
1085.24 129.57 869.522 89.381 653.798 89.381 c
653.798 89.381 l
438.074 89.381 222.355 129.57 6.636 129.57 c
6.636 129.57 l
6.636 118.482 l
222.355 118.482 443.553 76.908 659.275 76.908 c
659.275 76.908 l
874.996 76.908 1085.24 118.482 1300.958 118.482 c
1300.958 118.482 l
1516.684 118.482 1732.404 76.899 1948.119 76.899 c
1948.119 76.899 l
2163.842 76.899 2375.31 115.709 2591.027 115.709 c
2591.027 115.709 l
2806.745 115.709 3026.721 79.671 3242.446 79.671 c
3242.446 79.671 l
3458.165 79.671 3673.886 118.482 3889.606 118.482 c
3889.606 118.482 l
4105.324 118.482 4319.843 76.899 4535.563 76.899 c
4535.563 76.899 l
4751.28 76.899 4968.208 118.482 5183.928 118.482 c
5183.928 118.482 l
5183.928 129.57 l
4968.208 129.57 4743.972 93.532 4528.255 93.532 c
W n
q
0 g
1 0 0 -1 0 0 cm
BX /Sh1 sh EX Q
Q
BT
0 0 0 0 k
/TT1 1 Tf
32.8569 0 0 33.4258 1715.6987 25.8945 Tm
(IONICS Mass Spectrometry )Tj
31.0315 0 0 31.5688 2285.5337 26.5742 Tm
(32 Nixon Road, Bolton, Ontario, Canada)Tj
32.8569 0 0 33.4258 3441.6553 27.1172 Tm
[(www)37(.ionics.ca)]TJ
-13.172 -0.056 Td
(Info@ionics.ca)Tj
0.971 0.736 0.017 0 k
35 0 0 35 2036.4316 1205.208 Tm
[(Extracted Ion Chromatograms of Fou)1(r Mixed Compounds in Diluted Urine)]TJ
2.602 23.477 Td
[(LC-MRM Chromatograms of Fentanyl and Norfentanyl in W)37(ater)]TJ
ET
0 0 0 0.9 k
q 1 0 0 1 2021.6011 1991.6674 cm
0 0 m
1252.799 0 l
h
f
Q
q
0 2592 5184 -2592 re
W n
q 1 0 0 1 3274.3994 1995.1675 cm
0 0 m
-60.8 0 l
-219.489 0 l
-440.505 0 l
-688.282 0 l
-927.257 0 l
-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
-60.8 0 l
-219.489 0 l
-440.505 0 l
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-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
f
Q
q 1 0 0 1 3274.3994 1167.2676 cm
0 0 m
-1252.799 0 l
h
f
Q
q 1 0 0 1 3274.3994 1170.7676 cm
0 0 m
-60.8 0 l
-219.489 0 l
-440.505 0 l
-688.282 0 l
-927.257 0 l
-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
-60.8 0 l
-219.489 0 l
-440.505 0 l
-688.282 0 l
-927.257 0 l
-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
f
Q
Q
BT
0 0 0 1 k
/TT0 1 Tf
30 0 0 30 285.7441 1541.8984 Tm
[(Sample and Preparation: )17(The Fentanyl, Norfentanyl, Pentazocine and Meperidine standard stock sol\
utions in )]TJ
T*
[(liquid form were purchased from Cerilliant Inc \(Round Rock, )15(T)111(exas\) and stored at )]TJ
/T1_0 1 Tf
(-)Tj
/TT0 1 Tf
(20\260C. For sensitivity test, the )Tj
T*
(low level of pure Fentanyl and Norfentanyl standards were prepared by di\
luting the high concentration stock )Tj
T*
[(with 50/50 water/methanol in 0.1% formic acid. )17(The drug free urine was purchased from UT)73(AK \(V)74(alencia, CA\). )]TJ
T*
[(The urine was cleaned up by centrifuge for 15 minutes and the supernatan\
t was filtered by 0.2\265m filter)51(, then it is )]TJ
T*
[(diluted by 0.1% formic acid 1000 times and used as urine matrix. )16(The calibration standards were prepared by )]TJ
T*
(making an addition of ten microliters of working solution to the diluted\
urine to obtain required concentration )Tj
T*
(levels. )Tj
0 -2.4 TD
[(LC-MS/MS Conditions: )17(The LC-MS/MS was performed using IONICS\222)36( 3Q 200 Series,a triple quadrupole mass )]TJ
0 -1.2 TD
[(spectrometer \(Bolton, ON Canada\) with a Shimadzu UFLC system. Sample i\
njections of 10\265L)34( were loaded on a )]TJ
T*
[(Imtakt Cadenza CD-C18HT)17( column \(50x2.0mm, 3\265m\) using the gradient \(60% B isocratic for se\
nsitivity test\) as )]TJ
T*
[(shown below at a flow rate of 0.5mL/min. Mobile phase )53(A: 5% MeOH, 95% H2O, 0.1% Formic )55(Acid,5mM )]TJ
T*
[(NH4OAc; Mobile phase B: 95% MeOH,5% H2O, 0.1% Formic )54(Acid, 5mM NH4OAc. )18(The mass spec ion source )]TJ
T*
[(settings are: Electrospray V)55(oltage = 5000V)91(, HSID=250\260C, Nebulizer Gas=450, Drying Gas=200, Heating )]TJ
T*
[(gas=350, Source temperature =325\260C. )54(And the optimized MRM parameters for all analytes are shown in the )]TJ
T*
(following table.)Tj
ET
q
342.464 558.53 359.999 359.64 re
W n
q
/GS3 gs
359.9999847 0 0 359.6404419 342.4638672 558.5304565 cm
/Im0 Do
Q
Q
q
813.356 560.333 702.24 354.841 re
W n
q
/GS3 gs
702.2399902 0 0 354.841095 813.3554688 560.3337097 cm
/Im1 Do
Q
Q
BT
/TT0 1 Tf
30 0 0 30 2093.1108 1931.8198 Tm
[(Fentanyl: blank, 250 and 500ag/\265L)35( in duplicate injections )]TJ
0.599 -12.431 Td
[(Norfentanyl: blank, 250 and 500ag/\265L)35( in duplicate injections )]TJ
ET
q
2068.964 909.686 1204.08 180 re
W n
q
1204.0801849 0 0 180 2068.9643555 909.6865234 cm
/Im2 Do
Q
Q
q
2075.944 688.721 1224.119 180 re
W n
q
1224.1194611 0 0 179.9999847 2075.9443359 688.7216949 cm
/Im3 Do
Q
Q
q
2081.004 463.756 1212 180 re
W n
q
1212.0001678 0 0 180.0001221 2081.0043945 463.7567139 cm
/Im4 Do
Q
Q
q
2082.284 245.76 1213.439 198 re
W n
q
1213.4394073 0 0 198.0000305 2082.284668 245.7597351 cm
/Im5 Do
Q
Q
BT
/TT0 1 Tf
30 0 0 30 2117.771 1100.6836 Tm
(Fentanyl \(1 fg/\265L, retention time = 2.46 min)Tj
-0.668 -7.4 Td
[(Norfentanyl \(1 fg/\265L, retention time = 2.24)-1( min\) )]TJ
-0.001 -7.267 Td
[(Pentazocine \(4 fg/\265L, retention time = 2.3)-1(9 min)]TJ
0.399 -7.435 Td
[(Meperidine \(2 fg/\265L, retention time = 2.34)-1( min\) )]TJ
0.971 0.736 0.017 0 k
/TT1 1 Tf
35 0 0 35 4057.4336 2025.2256 Tm
(Calibration Curves)Tj
ET
q
0 2592 5184 -2592 re
W n
0 0 0 0.9 k
q 1 0 0 1 4839.4277 1987.2856 cm
0 0 m
-1252.799 0 l
h
f
Q
q 1 0 0 1 4839.4277 1990.7856 cm
0 0 m
-60.8 0 l
-219.489 0 l
-440.505 0 l
-688.282 0 l
-927.257 0 l
-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
-60.8 0 l
-219.489 0 l
-440.505 0 l
-688.282 0 l
-927.257 0 l
-1121.866 0 l
-1236.545 0 l
-1252.799 0 l
-1257.313 0 -1257.313 -7 -1252.799 -7 c
-1191.999 -7 l
-1033.31 -7 l
-812.294 -7 l
-564.517 -7 l
-325.542 -7 l
-130.933 -7 l
-16.254 -7 l
0 -7 l
4.515 -7 4.515 0 0 0 c
f
Q
Q
q
3577.304 1516.513 614.754 406.08 re
W n
q
614.7542267 0 0 406.0806122 3577.3046875 1516.5126495 cm
/Im6 Do
Q
Q
q
3579.947 1045.269 602.993 406.44 re
W n
q
602.9938354 0 0 406.4410706 3579.9462891 1045.2684021 cm
/Im7 Do
Q
Q
q
4368.028 1516.258 574.498 412.56 re
W n
q
574.4971161 0 0 412.5598755 4368.0292969 1516.2579956 cm
/Im8 Do
Q
Q
q
4384.5 1046.432 568.498 398.161 re
W n
q
568.4970703 0 0 398.161499 4384.5009766 1046.4317627 cm
/Im9 Do
Q
Q
BT
0 0 0 1 k
/TT0 1 Tf
30 0 0 30 3626.9248 968.6699 Tm
(The calibration curves generated for Fentanyl \(377.3/188.1\), Norfentan\
yl \(233.3/84.1\), Pentazocine )Tj
T*
(\(286.3/69.1\) and Meperidine\(248.3/220.1\) with triplet injections usi\
ng 1/x weighting showed good lin)Tj
44.027 0 Td
(-)Tj
-44.027 -1.2 Td
(earity \(R2 > 0.999\) up to 4 orders of magnitude in concentrations rang\
ing from low femtograms per mi)Tj
44.938 0 Td
(-)Tj
-44.938 -1.2 Td
[(croliter to 10,000 fg/\265L. )18(The average accuracy and CV% at LLOQ are 99.1% and 15.5% for Fentanyl, )]TJ
T*
[(94.5% and 13.0% for Fentanyl, 104.4% and 18.2% for Pentazocine, 106.7% a\
nd 1)71(1.6% for Meperi)]TJ
43.398 0 Td
(-)Tj
-43.398 -1.2 Td
[(dine, respectively)73(. )]TJ
0 -2.4 TD
(The matrix is minimized by diluting the urine \(a thousand times in pres\
ent study\) and an excellent )Tj
0 -1.2 TD
(specificity is maintained through the LLOQs.)Tj
0.2 -5.101 Td
[(A)55( detection limit in the attogram level is found for Fentanyl and Norfent\
anyl with IONICS 3Q 200 )]TJ
T*
[(series Molecular )54(Analyzer triple quadrupole mass spectrometer)53(.)]TJ
0 -2.4 TD
[(A)55( fast, sensitive, and accurate LC-MS/MS method based on \223dilute and s\
hoot\224 methodology for Fen)]TJ
43.913 0 Td
(-)Tj
-43.913 -1.2 Td
[(tanyl, Norfentanyl, Pentazocine and Meperidine using IONICS 3Q 200 serie\
s Molecular )51(Analyzer was )]TJ
0 -1.2 TD
[(developed. )17(The LLOQs achieved for these compounds in diluted urine were at low femt\
ogram per mi)]TJ
44.45 0 Td
(-)Tj
-44.45 -1.2 Td
[(croliter levels with 10\265L)36( injection. Excellent linearity over four orders of magnitude in concent\
ration is )]TJ
T*
[(also obtained with good precision and accuracy for these compounds . )15(This method requires little )]TJ
T*
(sample preparation and is well-suited for routine drug of abuse quantita\
tion.)Tj
3.25 56.655 Td
(Fentanyl: 1 to 10,000 fg/\265L)Tj
24.886 0.101 Td
(Norfentanyl: 1 to 10,000 fg/\265L)Tj
-25.852 -15.752 Td
(Pentazocine: 4 to 10,000 fg/\265L)Tj
26.853 -0.501 Td
[(Meperidine: 2 to 10,000 fg/\265L)36( )]TJ
0 0 0 0 k
70 0 0 70 875.6484 2410.1792 Tm
[(Simple and Rapid Method Development for High )15(Throughput )55(Analysis of Pain Management Drugs in Urine by LC-MS/MS)]TJ
0 0 0 1 k
30 0 0 30 2321.8115 2297.8042 Tm
[(Sha Joshua )18(Y)92(e ; Frenny Ruparelia; George Scott)]TJ
-3.776 -1.2 Td
(IONICS Mass Spectrometry Group, Inc, Bolton, Ontario, CANADA)Tj
ET
q
0 2592 5184 -2592 re
W n
q 1 0 0 1 2321.7915 2292.2813 cm
0 0 m
204.021 0 l
f
Q
q 1 0 0 1 2320.4507 2290.916 cm
0 0 m
146.945 0 l
204.021 0 l
205.327 0 209.341 2.73 206.702 2.73 c
59.757 2.73 l
2.682 2.73 l
1.375 2.73 -2.639 0 0 0 c
f
Q
Q
q
/GS3 gs
1199.9999695 0 0 246 2031.5209961 1636.4350586 cm
/Im10 Do
Q
BT
0 0.988 1 0 k
/TT2 1 Tf
26.04 0 0 26.04 2216.8828 1695.6133 Tm
(B)Tj
0.668 0 Td
(l)Tj
0.277 0 Td
(a)Tj
0.443 0 Td
(n)Tj
0.502 0 Td
(k)Tj
11.403 2.527 Td
(2)Tj
0.502 0 Td
(5)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(a)Tj
0.443 0 Td
(g)Tj
0.502 0 Td
(/)Tj
0.277 0 Td
(\265)Tj
(L)Tj
13.568 2.875 Td
(5)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(a)Tj
0.443 0 Td
(g)Tj
0.502 0 Td
(/)Tj
0.277 0 Td
(\265)Tj
(L)Tj
0.84 0.129 1 0.027 k
-18.165 -4.518 Td
(S)Tj
0.557 0 Td
(/)Tj
0.277 0 Td
(N)Tj
0.723 0 Td
(=)Tj
0.563 0 Td
(6)Tj
13.746 2.876 Td
(S)Tj
0.557 0 Td
(/)Tj
0.277 0 Td
(N)Tj
0.723 0 Td
(=)Tj
0.563 0 Td
(1)Tj
0.502 0 Td
(3)Tj
ET
q
2033.51 1259.66 1200.239 255.601 re
W n
q
/GS3 gs
1200.239975 0 0 255.5999908 2033.5102539 1259.6607513 cm
/Im11 Do
Q
Q
BT
0 0.988 1 0 k
/TT2 1 Tf
26.04 0 0 26.04 2200.5278 1341.1563 Tm
(B)Tj
0.668 0 Td
(l)Tj
0.277 0 Td
(a)Tj
0.443 0 Td
(n)Tj
0.502 0 Td
(k)Tj
11.987 2.528 Td
(2)Tj
0.502 0 Td
(5)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(a)Tj
0.443 0 Td
(g)Tj
0.502 0 Td
(/)Tj
0.277 0 Td
(\265)Tj
(L)Tj
13.434 2.875 Td
(5)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(0)Tj
0.502 0 Td
(a)Tj
0.443 0 Td
(g)Tj
0.502 0 Td
(/)Tj
0.277 0 Td
(\265)Tj
(L)Tj
0.84 0.129 1 0.027 k
-18.031 -4.518 Td
(S)Tj
0.557 0 Td
(/)Tj
0.277 0 Td
(N)Tj
0.723 0 Td
(=)Tj
0.563 0 Td
(6)Tj
13.612 2.876 Td
(S)Tj
0.557 0 Td
(/)Tj
0.277 0 Td
(N)Tj
0.723 0 Td
(=)Tj
0.563 0 Td
(1)Tj
0.502 0 Td
(3)Tj
ET
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