Testing robustness: Immunosuppressant drugs in blood with a TSQ Quantis MS for clinical research

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TEHNIL NOTE 64969 Testing robustness: Immunosuppressant drugs in blood with a TSQ Quantis MS for clinical research uthors Kristine Van Natta, Neloni Wijeratne, laudia Martins Thermo Fisher Scientific, San Jose, Keywords Immunosuppressant, tacrolimus, sirolimus, everolimus, cyclosporin, TSQ Quantis MS, TraceFinder, clinical research, robustness Goal Demonstrate the robustness of the Thermo Scientific TSQ Quantis triple quadrupole mass spectrometer by analysis of immunosuppressant drugs in whole blood for clinical research. Introduction Mass spectrometry is a popular choice of technology in clinical research for the quantitation of immunosuppressant drugs in whole blood. sensitive and robust instrument is required for reliable quantitation workflows. In this study, we demonstrate the TSQ Quantis triple quadrupole mass spectrometer for this application. Experimental Sample preparation alibrators and controls were obtained from REIPE hemicals + Instruments GmbH (Munich, Germany). lank whole blood was obtained from ioreclamationivt (New York, US). riefly, whole blood calibrators, controls, and 1 different lots of blank whole blood were processed by precipitation with ZnSO 4 /methanol solution containing internal standards (cyclosporin D and ascomycin). Samples were vortexed for one minute, left to stand for 3 minutes in a refrigerator, and centrifuged at 13, rpm for 1 minutes. Supernatant was transferred to an autosampler vial, and 15 µl was injected onto the HPL system. This processing method removes the majority of blood proteins but does not remove phospholipids.

Liquid chromatography hromatographic separation was performed using a Thermo Scientific Vanquish Flex inary HPL system. The column used was a Thermo Scientific Hypersil GOLD 8 L column (5 2.1 mm, 5 µm particle size) maintained at 8. Mobile phases and consisted of 1 mm ammonium formate with.1% formic acid in Fisher hemical Optima grade water and methanol, respectively. No divert valve was used. The total run time was 3 minutes. Mass spectrometry ompounds were detected on a TSQ Quantis triple quadrupole mass spectrometer equipped with a heated electrospray ionization source. The ion source was set to Medium (M) at position 2, with sweep gas set to 2 (arb units). ll the compounds formed an ammoniated adduct that was used as the precursor ion. Two selected reaction monitoring (SRM) transitions were monitored for each analyte and one was monitored for the internal standards. Dioctyl phthalate and three endogenous phospholipids were also monitored as surrogates for instrument cleanliness. Test of robustness The daily sequence of samples consisted of an initial set of eight calibrators. This was followed by repeated sets of five controls and 2 blank blood samples. set of calibrators was inserted approximately halfway through the total sequence and again at the end. The total number of samples per sequence was approximately 3. The sequence was repeated for five consecutive days. Peak areas of the internal standards and calculated concentration of the mid-level control were monitored for stability. Data analysis Data was acquired and processed using Thermo Scientific TraceFinder software. Figure 1 shows representative chromatograms for analytes at their respective LOQs and internal standards. Figure 1, 1, and 1. hromatograms for lowest calibration standard showing ion ratio confirmation. 2

D E F Figure 1D, 1E, and 1F. hromatograms for lowest calibration standard showing ion ratio confirmation along with internal standards. Results and discussion Linearity ll compounds were linear over their calibration ranges of approximately 2 6 ng/ml for tacrolimus, sirolimus, and everolimus, and 25 18 ng/ml for cyclosporin. Figure 2 shows representative calibration curves for all compounds. ll calibrators back-calculated to within 2% of theoretical values over the five days of testing. D Figure 2. Representative calibration curves. 3

Robustness Peak areas for cyclosporin D and ascomycin, the two internal standards used in this study, showed precisions of 4% and 8%, respectively, over the five days and over 15 injections (Figure 3). alculated concentration precisions for ontrol III for cyclosporin, everolimus, sirolimus, and tacrolimus were 2.36%, 4.22%, 4.8%, and 3.57%, respectively, over the five days (n=6 injections each) (Figure 4). Phospholipids showed no buildup over the course of the study. 3 25 2 15 1 5 3 25 yclosporin %RSD = 2.36 ±2% Peak rea 5, yclosporin D in Whole lood 25, 4.% RSD 2 15 1 5 Everolimus %RSD = 4.22 ±2% 3 9, scomycin Peak rea %V = 8.29% 25 Peak rea 7, 5, 3, 1, scomycin Peak rea ± 2% 1 145 29 435 58 725 87 115 116 135 1452 Injection # Figure 3. Raw peak area reproducibility across 5 days at approximately 3 injections per day from different batches of whole blood for () cyclosporin D internal standard and () ascomycin internal standard. 2 15 1 5 2 18 16 14 12 1 8 6 4 2 D Sirolimus %RSD = 4.8 ±2% Tacrolimus %RSD = 3.57 ±2% 14 2 4 6 8 1 12 1464 Injection # (12/day) Figure 4. Quality control precision for () cyclosporin, () everolimus, () sirolimus, and (D) tacrolimus, during 5-day robustness testing. Twelve Qs per day were injected throughout each day s run of approximately 3 samples. 4

onclusion The TSQ Quantis triple quadrupole MS demonstrated robust, reliable, and consistent performance for more than 15 samples over five days with no need for maintenance. alibrators and controls maintain precision and accuracy demonstrating reliability. The quantitative workflow exhibited reproducible results on a sensitive and robust platform suitable for analysis of immunosuppressant drugs in blood for clinical research. For Research Use Only. Not for use in diagnostic procedures. Find out more at thermofisher.com/ltis-quantis 217 Thermo Fisher Scientific Inc. ll rights reserved. ioreclamationivt is a registered trademark of ioreclamation-ivt Holdings, LL. ll other 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. TN64969-EN 517S