Development of analytical methods for Catecholamines, Metanephrines and related metabolites in urine and plasma matrices
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1 Development of analytical methods for Catecholamines, Metanephrines and related metabolites in urine and plasma matrices From sample preparation to LC/MS/MS Linda Côté Christophe Deckers Agilent Technologies
2 Outline Introduction Why a unified approach? Description of each method Sample preparation Chromatography Figures of merits Sample preparation Why Which sample preparation technique to choose Conclusions Questions and Answers 2
3 Which ones and in which matrix urine or plasma? 7 different methods Free catecholamines in urine Total metanephrines in urine Free catecholamines in plasma Free metanephrines in plasma VMA in urine HVA in urine 5-HIAA in urine 3
4 Why a unified approach? Challenge: Many analysis to perform with One LC/MS/MS system 4
5 Which ones and in which matrix urine or plasma? Webinar April 2013 Free catecholamines and metanephrines in urine Total catecholamines and metanephrines in urine Free catecholamines in plasma (in progress) Free metanephrines in plasma (in progress) VMA in urine (in progress) HVA in urine (in progress) 5-HIAA in urine (in progress) 5
6 Catecholamines and related metabolites in urine or plasma 4 methods with a unified approach Free catecholamines and metanephrines in urine Total catecholamines and metanephrines in urine Free catecholamines in plasma Free metanephrines in plasma VMA in urine HVA in urine 5-HIAA in urine
7 Unified approach in method development Matrix Linear range Sample prep Chromatography Mobile phase LC/MS/MS 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats 7
8 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Chromatography Mobile phase LC/MS/MS mg/l pg/ml pg/ml 8
9 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /6460 9
10 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
11 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
12 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
13 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
14 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
15 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
16 Catecholamines and metanephrines in a single run 16
17 Catecholamines and metanephrines in a single run One SPE cartridge is used to recover both catecholamines and metanephrines SPE Bond Elut Plexa was chosen for best recoveries Simple acid elution for direct injection into LC-MS/MS ph control for stabilization of catecholamines Metanephrines are also retained under the same conditions, even though they are methylated and do not contain the cis-diol moiety for the covalent linkage binding mechanism Studies have shown that metanephrines do have some affinity for this sorbent [1] Ann Clin Biochem 2009; 46: DOI: /acb
18 Sample preparation Calibrators are prepared with clean urine matrix from Golden West Biologicals Isotopically labelled Internal standards 24 hours collection of urine Native urine for free catecholamines and metabolites (typically for catecholamines) Acid-hydrolysed urine for total (typically for metanephrines) Solid phase extraction (SPE) is used to cleanup urine 18
19 Compound structures HO HO OH HO OH HO NH 2 HO NH 2 HO HN CH 3 Dopamine (D) C8H11NO2 Neutral Mass: Norepinephrine (NE) C8H11NO3 Neutral Mass: Epinephrine (E) C9H13NO3 Neutral Mass: CH 3 CH 3 OH CH 3 OH O O O HO NH 2 HO NH 2 HO HN CH 3 3-Methoxytyramine (3-MT) C9H13NO2 Neutral Mass: Normetanephrine (NMN) C9H13NO3 Neutral Mass: Metanephrine (MN) C10H15NO3 Neutral Mass:
20 Chromatography challenge Need to keep resolution between E and NMN Also between MN and 3-MT 20
21 Catecholamines and metanephrines in a single run Chromatography E/NMN and MN/3-MT Resolution is Critical 1. Norepinephrine (NE) 2. Epinephrine (E) 3. Normetanephrine (NMN) 4. Dopamine (D) 5. Metanephrine (MN) 6. 3-Methoxytyramine (3-MT) E D MN 3-MT NE NMN 21
22 Calibration curves 22
23 Results Summary of Analyte Performance Compound R 2 Concentration Concentration Dopamine Accuracy (%) Intraday CV (%) Interday CV (%) (ng/ml) (nmol/l) n = 3 n = 3 n = Norepinephrine Epinephrine Note: Signal to noise ratios and CVs indicate that LLOQs are lower than measured here for all analytes 23
24 Results Summary of Analyte Performance Compound R 2 Concentration Concentration 3-Methoxytyramine Accuracy (%) Intraday CV (%) Interday CV (%) (ng/ml) (nmol/l) n = 3 n = 3 n = Normetanephrine Metanephrine Note: Signal to noise ratios and CVs indicate that LLOQs are lower than measured here for all analytes 24
25 Results Inter-run Over 3 Days for Commercial QC (BioRad Lyphocheck) Level 1 Level 2 Compound Free/Total Range (HPLC) Measured CV (%) Range (HPLC) Measured CV (%) Dopamine Free Norepinephrine Free Epinephrine Free Methoxytyramine Total Normetanephrine Total Metanephrine Total All measurements are in ng/ml Bio-Rad QC material was used. Ranges provided were for free catecholamines and total metanephrines 25
26 Results Inter-run Over 3 Days for Commercial QC (BioRad Lyphocheck) Level 1 Level 2 Compound Free/Total Range (HPLC) Measured CV (%) Range (HPLC) Measured CV (%) Dopamine Free Norepinephrine Free Epinephrine Free Methoxytyramine Total Normetanephrine Total Metanephrine Total All measurements are in nmol/l Bio-Rad QC material was used. Ranges provided were for free catecholamines and total metanephrines 26
27 Results Recoveries Observed Using SPE Procedure Compound Absolute Recoveries %* (n = 9) Relative recoveries % With ISTDs corrections** (n = 9) Average SD Range Average SD Dopamine Norepinephrine Epinephrine Methoxytyramine Normetanephrine Metanephrine * ISTDs peak areas spiked in formic acid subjected to SPE compared with spiked formic acid without SPE ** Calculated concentrations with ISTDs peak area ratios corrections (with SPE) versus theoretical concentrations 27
28 Results Matrix Effects Observed Using SPE Procedure Compound Matrix effects %* (n = 9) Accuracies % With ISTDs corrections** (n = 9) Average SD Range Average SD Dopamine Norepinephrine Epinephrine Methoxytyramine Normetanephrine Metanephrine * ISTDs peak areas spiked in urine subjected to SPE compared with spiked formic acid subjected to SPE ** Calculated concentrations with ISTD corrections (urine with SPE) versus theoretical concentrations 28
29 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
30 Compound structures Vanillyl mandelic acid (VMA) C9H10O5 Neutral Mass: Hydroxyindole-3-acetic acid (5-HIAA) C10H9NO3 Neutral Mass: Homovanillic acid (HVA) C9H10O4 Neutral Mass:
31 Sample preparation Calibrators are prepared with clean urine matrix from Golden West Biologicals Isotopically labelled Internal standards 24 hours collection of urine Dilution of urine (vortex and centrifuge) 1 in 10 with 0.2% formic acid in water 31
32 Example chromatogram 2 1. VMA 2. 5-HIAA 3. HVA
33 Calibration curves 33
34 Results Summary of Analyte Performance Compound R 2 Concentration Concentration VMA Accuracy (%) Intraday CV (%) Interday CV (%) (mg/l) (µmol/l) n = 3 n = 3 n = HIAA HVA Note: Signal to noise ratios and CVs indicate that LLOQs are lower than measured here for all analytes 34
35 Results Inter-run Over 3 Days for Commercial QC (BioRad Lyphocheck) Compound Range (HPLC) Level 1 Level 2 Measured CV (%) Range (HPLC) Measured CV (%) VMA HIAA HVA All measurements are in mg/l (n=5) Bio-Rad QC material was used. Ranges provided were for HPLC method 35
36 Results Matrix Effects Observed Compound Matrix effects %* (n = 10) Accuracies % With ISTDs corrections** (n = 10) Average SD Range Average SD VMA HIAA HVA Measurements done at 10 different concentrations ranging from to 100 mg/l * Peak areas from urine spiked compared with 0.2% formic acid-h2o solutions spiked ** Calculated concentrations of urine spiked with ISTD corrections versus theoretical concentrations 36
37 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
38 Sample preparation Calibrators are prepared with clean plasma matrix from Golden West Biologicals Isotopically labelled Internal Standards Solid phase extraction (SPE) is used to cleanup plasma 38
39 Plasma calibrator chromatogram with extra wash 1. Normetanephrine 2. Metanephrine 3. 3-Methoxytyramine
40 Calibration curves 40
41 Results Summary of analyte performance Compound R 2 Concentration Concentration Accuracy (%) Intraday CV (%) Interday CV (%) (pg/ml) (nmol/l) n = 3 n = 3 n = Methoxytyramine Normetanephrine Metanephrine
42 Results Inter-run over 3 days for commercial QC materials (ChromSystems) Level 1 (n=3) Level 2 (n=3) Compound Measured (pg/ml) CV (%) Measured (pg/ml) CV (%) 3-Methoxytyramine Normetanephrine Metanephrine
43 Results SPE extraction procedure recoveries with spiked formic acid solutions with and without SPE Compound Absolute Recoveries %* (n = 9) Relative recoveries % With ISTDs corrections** (n = 9) Average SD Range Average SD 3-Methoxytyramine Normetanephrine Metanephrine *: Peak areas spiked in formic acid subjected to SPE compared with spiked formic acid without SPE **: Calculated concentrations with ISTDs peak area ratios corrections (with SPE) versus theoretical concentrations 43
44 Results Matrix effect and Recovery efficiency Compound Matrix effects % (n = 9) Recovery efficiency % (n = 9) Average SD Average SD 3-Methoxytyramine Normetanephrine Metanephrine A: neat standard solutions B: plasma extracted then spiked (post-ext) C: spiked plasma then extracted (pre-ext) Matrix effect % = B/A * 100 Recovery efficiency % = C/B *
45 Unified approach in method development 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Chromatography Pursuit-PFP Pursuit-PFP Pursuit-PFP Pursuit-PFP Mobile phase 0.2% formic acid - Methanol 0.2% formic acid - Methanol 0.2% formic acid - Methanol 1 mm ammonium fluoride - Methanol LC/MS/MS 1290/ / / /
46 Sample preparation Challenge: Need to measure low pg/ml in plasma, therefore must cleanup and concentrate Calibrators are prepared with clean plasma matrix from Golden West Biologicals Isotopically labelled Internal Standards Catecholamines are readily oxidized and unstable in whole blood and plasma. Stabilizers should be added to plasma. Step 1: Protein precipitation and lipids removal with Captiva ND Lipids filter cartridges Step 2: Solid phase extraction (SPE) is used to further cleanup plasma 46
47 Sample Preparation Plasma pretreatment Pretreatment of samples: Plasma should be kept frozen at -80 C until sample analysis Stabilizer solutions: Sodium metabisulfite: 317 mg/ml of sodium metabisulfite in water EDTA 0.5M For sample plasma, calibrators and QCs Add 2% v/v of each stabilizer solution 47
48 Method LC Conditions (1290) Column: Analytical: Guard: Pursuit 3 PFP, 2 x 150 mm, 3 µm Pursuit 3 PFP MetaGuard 2 mm Column Temp: 30 C Injection volume: 20 µl Needle Wash: 1:1:1:1 MeOH:ACN:IPA:H 2 O + 0.1% formic acid 20 seconds Injector Temp: 4 C Mobile Phase: Flow rate: 1290 Pump Gradient: A: 1 mm Ammonium Fluoride in Water B: Methanol 0.3 ml/min. Time (min) %B Stop time: 10 min. Requilibration time: 3 min. 48
49 Plasma Catecholamines calibrator chromatogram 3 1. Norepinephrine 2. Epinephrine 3. Dopamine
50 Calibration curves 50
51 Results Summary of analyte performance Compound R 2 Concentration Concentration Accuracy (%) Inter-day CV (%) n = 3 (pg/ml) (nmol/l) n = 3 n = Norepinephrine Epinephrine Dopamine
52 Results Intra and Inter-day over 3 days for commercial QC materials (ChromSystems) Compound QC Level Measured Value Intra-day (n=3) pg/ml - nmol/l Intra-day CV% (n=3) Measured Value Inter-day (n=3) pg/ml - nmol/l Inter-day CV% (n=3) Norepinephrine Epinephrine Dopamine
53 Results Matrix effect and Recovery efficiency Compound Matrix effects % (n = 3) Recovery efficiency % (n = 3) Average SD Average SD Norepinephrine Epinephrine Dopamine A: neat standard solutions B: plasma extracted then spiked (post-ext) C: spiked plasma then extracted (pre-ext) Matrix effect % = B/A * 100 Recovery efficiency % = C/B *
54 Sample preparation Why Which sample preparation technique to choose 54
55 Objectives of Sample Preparation Removal of interferences that affect detection and accuracy Reach lower detection limits Increase method robustness Decrease overall operating costs 55
56 Types of Interferences in Biological Samples Major causes of matrix effects: Salts generally elute early in the run Abundant Proteins most prominent interference Lipids, phospholipids, and lysophosphatidylcholines difficult to remove Surfactants, dosing agents, excipients Phthalates and plasticizers from plastic ware 56
57 Instrumentation affects selection of Sample Preparation Techniques More Specific Instrument Separation and Detection Specificity Less Specific Less Specific Sample Preparation Specificity More Specific Sample Prep Technique Interference Removed Dilute & Shoot Filtration Liquid/Liquid Extractions Supported Liquid Extractions (SLE) Dried Matrix Spotting Precipitation QuEChERS Lipid Removal Hybrid' Filtration Solid Phase Extraction Lipids No No No Some No No Yes Yes Yes Oligomeric Surfactants No No No No No No No Yes Yes Particulates No Yes No Some No Yes Yes Yes Yes Pigments No No No Some No No Yes No Yes Polar Organic Acids No No Yes Yes No No Yes No Proteins No No Yes Yes Yes Yes Yes Yes Yes Salts No No Yes Yes No No No No Yes Suggested Agilent Product Agilent Autosampler Vials Captiva Syringe Filters Chem Elut Captiva ND Bond Elut QuEChERS Captiva ND LIPIDS Bond Elut Silica and Polymeric SPE 57
58 Why did we use different sample preparation techniques? 1. Free and Total Cats/Mets 2. VMA, HVA, 5- HIAA 3. Mets 4. Cats Matrix Urine Urine Plasma Plasma Linear range ng/ml Sample prep Boronate complex/ Bond Elut Plexa SPE mg/l pg/ml pg/ml Dilution WCX SPE Captiva ND Lipids / BondElut PBA SPE Analyte Dependant HO CH 3 O OH HO NH 2 HO HN CH 3 Sample Dependant 58
59 Why did we use different sample preparation techniques? Consideration 1: Sample type (Urine vs Plasma) The dirtier the sample, the better sample cleanup you need to remove interferences If the sample matrix is not removed you may have: carry-over, lipid build-up, ion suppression, low signal to noise ratio A dirty sample increases operational costs, impacting instrument maintenance, sample re-runs, column lifetime Consideration 2: Analyte characteristics and LLOQs To reach pg/ml levels, you need a sample prep technique that concentrates the analyte The analyte s chemical properties are unique (Polarity, Log P, pka, solubility) Some analytes have stability limitations 59
60 What is Solid Phase Extraction (SPE) Four steps to Selective cleanup and Elution Green = Blue and Yellow Blue is more non polar than yellow Blue is retained Sample loading Retention Rinsing Elution 60
61 Catecholamines and metanephrines in urine Solid Phase Extraction (SPE) Prepare complexed samples: 0.5 ml urine*, calibrators, QCs* Add 40 µl of internal standards mix Add 0.8 ml of Diphenyl-Boronate complexing agent Verify ph, must be between If necessary adjust to ph 8.5 with NH4OH Step 1: Step 2: Step 3: Step 4: Condition SPE cartridge (Bond Elut Plexa, 30 mg, 3 ml) with: 1 ml of MeOH 1 ml of wash buffer 0.2 M NH4Cl-NH4OH Add complexed samples Wash with 1 ml of 5% MeOH wash buffer 0.2 M NH4Cl-NH4OH Dry at full vacuum for 5 minutes Elute with 1 ml of 5% formic acid in water. Apply vacuum 5 Hg for 30 seconds Transfer to autosampler vial * Native for free catecholamines, hydrolyzed for total metanephrines (add 25 µl HCl 6N, incubate at 90 deg. C for 25 min., cool at RT) [1] Ann Clin Biochem 2009; 46: DOI: /acb [2] Talwar et al., Journal of Chromatography B, 769 (2002)
62 Diphenyl boronate-catecholamine complex The diphenyl boronate forms a stable negatively charged complex (Fig. 1) with cishydroxyl groups of catecholamines, which is strongly retained on a C18 extraction sorbent when operating in alkali media. This allows for column washing with methanol-buffer solutions to remove interfering compounds without the loss of the catecholamines which are eluted by disrupting the complex under acid conditions. [2] Talwar et al., Journal of Chromatography B, 769 (2002)
63 Metanephrines in plasma Pretreatment of samples: 0.5 ml plasma, calibrators, QCs Add 50 µl of internal standards mix Add 0.5 ml of 10 mm NH4H2PO4 buffer ph 6.5 Step 1: Step 2: Step 3: Step 4: Condition SPE cartridge (SampliQ WCX, 30 mg, 1 ml) with: 1 ml of MeOH 1 ml of 10 mm NH4H2PO4 buffer ph 6.5 Add samples Wash with 1 ml H2O, 1 ml Methanol, 1 ml 0.2% formic acid in acetonitrile Dry at full vacuum for 5 minutes Elute with 2 x 250 µl of 2% formic acid in acetonitrile. Apply vacuum 5 Hg for 60 seconds Evaporate under nitrogen flow at 40 deg. C Reconstitute with 100 µl of 0.2% formic acid in water 65
64 Catecholamines in plasma Step 1 Protein precipitation and lipids removal Add 1.5 ml of 0.5% formic acid in acetonitrile to a Captiva ND Lipids cartridge (3 ml, PN: A ) or plate Add 50 µl of internal standard solution Add 750 µl of pretreated sample plasma or calibrators or QCs Mix 3-5 times with a 1.5 ml empty pipette tip Wait 5-10 minutes Place under vacuum at 7 Hg for 2 minutes, then at 15 Hg until dry Use filtrate for SPE 66
65 Captiva ND Lipids Lipid removal and filtration principles Features: - Captiva particulate filter removes protein interferences - Proprietary Lipid Stripping Media removes lipids - Non-Drip Membrane ease of use 67
66 Catecholamines in plasma Step 2 Solid Phase Extraction (SPE) Pretreatment of samples: Use filtrate from step 1 Add 2 ml of 100 mm NH4H2PO4 buffer ph 10 1: Condition SPE cartridge (BondElut PBA, 100mg, 3 ml, PN: ) with: 1 ml acetonitrile 1 ml 5% formic acid in methanol 1 ml 100 mm NH4H2PO4 buffer ph 10 2: Add pretreated samples 3: Wash with: 2 ml 1% NH4OH in 95% methanol 2 ml 1% NH4OH in 95% acetonitrile 2 ml 1% NH4OH in 30% acetonitrile Dry at full vacuum for 5 minutes 4: Elute with: 3 x 500 µl of 5% formic acid in methanol Apply vacuum 5 Hg for 60 seconds Evaporate under nitrogen flow at 35 deg. C Reconstitute with 100 µl of 0.1% formic acid in water 68
67 Conclusions A unified approach where the same chromatography principles and the same modern LC/MS/MS instrumentation were used to analyze different compounds and matrices Novel and selective sample preparation techniques were adapted to the matrix and to the desired LLOQ Four analytical methods that are robust, sensitive and precise were developed 69
68 More information EN EN EN EN 70
69 Questions Thank You! For more information on Agilent s Clinical Research Solutions, visit 71
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