Simultaneous Quantitative Analysis of Total Catecholamines and Metanephrines in Urine Using 500 MG CLEAN UP CCX2 and LC-MS/MS

Similar documents
Simultaneous Quantitative Analysis of Total Catecholamines and Metanephrines in Urine Using CLEAN UP CCX2 and LC-MS/MS

Identification and Quantification of Psychedelic Phenethylamine 2C Series using SPE and LC-MS/MS

Simultaneous Determination of Prescription and Designer Benzodiazepines in Urine and Blood by SPE and LC-MS/MS

Extraction of Synthetic and Naturally Occurring Cannabinoids in Urine Using SPE and LC-MS/MS

Determination of Patulin in Apple Juice Using SPE and UHPLC-MS/MS Analysis

UCT STYRE SCREEN INNOVATION THROUGH CHEMISTRY

Analysis of Limonin in Citrus Juice Using QuEChERS and LC-MS/MS

Comprehensive Study of SLE as a Sample. Preparation Tool for Bioanalysis

Determination of Pharmaceutical Residues in Bovine Milk via LC MS/MS Following Solid Phase Extraction

High Throughput Extraction of Opiates from Urine and Analysis by GC/MS or LC/MS/MS)

Determination of 78 Banned or Controlled Racing Industry Drugs in Horse Urine Using SPE and LC-MS/MS

Abstract. Introduction

Rapid and Robust Detection of THC and Its Metabolites in Blood

Application Note. Abstract. Authors. Pharmaceutical

Determination of β2-agonists in Pork Using Agilent SampliQ SCX Solid-Phase Extraction Cartridges and Liquid Chromatography-Tandem Mass Spectrometry

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

The Raptor HILIC-Si Column

Reduced Ion Suppression and Improved LC/MS Sensitivity with Agilent Bond Elut Plexa

Performance of an ultra low elution volume 96-well plate

SPE-LC-MS/MS Method for the Determination of Nicotine, Cotinine, and Trans-3-hydroxycotinine in Urine

Extraction of Multiple Mycotoxins From Nuts Using ISOLUTE Myco prior to LC-MS/MS Analysis

Extraction of Aflatoxin M1 From Infant Formula Using ISOLUTE Myco SPE Columns prior to LC-MS/MS Analysis

Determination of Chlorophenoxyacetic Acid and Other Acidic Herbicides Using a QuEChERS Sample Preparation Approach and LC-MS/MS Analysis

UCT SELECTRA C18 HPLC COLUMN INNOVATION THROUGH CHEMISTRY

Using Hydrophilic Interaction Chromatography (HILIC) for the Retention of Highly Polar Analytes

Surviving Matrix Effects Experiments. Grace van der Gugten St. Paul s Hospital, Vancouver, BC, Canada

A RAPID AND SENSITIVE ANALYSIS METHOD OF SUDAN RED I, II, III & IV IN TOMATO SAUCE USING ULTRA PERFORMANCE LC MS/MS

Determination of Tetracyclines in Chicken by Solid-Phase Extraction and High-Performance Liquid Chromatography

Systematic Evaluation of Solid Phase Extraction (SPE) Chemistries for the Determination of Acidic, Neutral, and Basic Drugs

Extraction of Multiple Mycotoxins From Grain Using ISOLUTE Myco prior to LC-MS/MS Analysis

A Comprehensive Screening of Illicit and Pain Management Drugs from Whole Blood Using SPE and LC/MS/MS

A Novel Solution for Vitamin K₁ and K₂ Analysis in Human Plasma by LC-MS/MS

Institute of Toxicology Clinical Toxicology and Pharmacology Berliner Betrieb für Zentrale Gesundheitliche Aufgaben, Berlin

Pesticide Residue Analysis in Whole Milk by QuEChERS and LC-MS/MS

Comparison of Different Whole Blood Sample Pretreatment Methods for Targeted Analysis of Basic Drugs

Strata -X Polymeric SPE

LC-MS/MS analysis of Chlorates in Milk and Whey Powder using the Agilent 6470 QQQ

LC/MS/MS Analysis of Metabolites of Synthetic Cannabinoids JWH-018 and JWH-073 in Urine

Comprehensive Forensic Toxicology Screening in Serum using On-Line SPE LC-MS/MS

Fig. 1: Chemical structure of arachidonic acid COOH CH 3

E XCEL LENCE JUST GOT BETTER UCT FORENSICS CLEAN SCREEN XCEL SPE COLUMNS

Analysis of Cholesterol-Lowering Drugs (Statins) Using Dried Matrix Spot Technology

Authors. Abstract. Forensic Toxicology. Irina Dioumaeva, John M. Hughes Agilent Technologies, Inc.

Application Note. Author. Abstract. Introduction. Food Safety

A Robustness Study for the Agilent 6470 LC-MS/MS Mass Spectrometer

Rapid and Accurate LC-MS/MS Analysis of Nicotine and Related Compounds in Urine Using Raptor Biphenyl LC Columns and MS-Friendly Mobile Phases

LC-MS/MS Method for the Determination of Tenofovir from Plasma

Authors. Abstract. Introduction. Environmental

Analysis of Rosuvastatin in Dried Blood Spot and Plasma Using ACQUITY UPLC with 2D Technology

LC/MS/MS of Trichothecenes and Zearalenone in Wheat Using Different Sample Prep Methods

Vitamin D Metabolite Analysis in Biological Samples Using Agilent Captiva EMR Lipid

Determination of Ractopamine and Clenbuterol in Beef Samples

Fast quantitative Forensic Analysis of THC and its Metabolites in Biological Samples using Captiva EMR- Lipid and LC/MSMS

EASIMIP TM PATULIN Product Code: P250 / P250B

Detection of Low Level of Chloramphenicol in Milk and Honey with MIP SPE and LC-MS-MS

Quantification of lovastatin in human plasma by LC/ESI/MS/MS using the Agilent 6410 Triple Quadrupole LC/MS system

4.5 Minute Analysis of Benzodiazepines in Urine and Whole Blood Using LC/MS/MS and an Ultra Biphenyl Column

Author. Introduction. Small Molecule Pharmaceuticals & Generics

GlycanPac AXH-1 Columns

What You Can t See Can Hurt You. How MS/MS Specificity Can Bite Your Backside

Raptor HILIC-Si: Simplify the Switch to HILIC

Improved Isolation and Analysis of Mycotoxins from Cereals, Beer and Wine

Analyze Barbiturates in Urine with Agilent 6430 LC/MS/MS and Poroshell 120 EC-C18

SPE Cartridges. All Finneran Products Are Certified. Conditioning Sample application Wash Elution

Detection, Confirmation, and Quantification of Chloramphenicol in Honey, Shrimp and Chicken Using the Agilent 6410 LC/MS Triple Quadrupole

Amphetamines, Phentermine, and Designer Stimulant Quantitation Using an Agilent 6430 LC/MS/MS

Enrichment of Phospholipids from Biological Matrices with Zirconium Oxide-Modified Silica Sorbents

Integration of steroids analysis in serum using LC-MS/MS with full-automated sample preparation

LCMS Vitamin D3 Method development

HVA, VMA and 5-HIAA in Urine

Fast and simultaneous analysis of ethanol metabolites and barbiturates using the QTRAP 4500 LC-MS/MS system

The Ephedra Story: An Automated SPE Procedure and Analysis for the Determination of Ephedra and Ephedra-like Compounds in Dietary Supplements

Dienes Derivatization MaxSpec Kit

Raptor HILIC-Si: Simplify the Switch to HILIC

The Development of LC/MS Methods for Determination of MDMA (Ecstasy) and Metabolites in Biological Samples

Robust extraction, separation, and quantitation of structural isomer steroids from human plasma by SPE-UHPLC-MS/MS

Analytical Method for 2, 4, 5-T (Targeted to Agricultural, Animal and Fishery Products)

O O H. Robert S. Plumb and Paul D. Rainville Waters Corporation, Milford, MA, U.S. INTRODUCTION EXPERIMENTAL. LC /MS conditions

Comparison of Biotage Extrahera vs. Manual Sample Processing Using a Vacuum Manifold

Dr. Erin E. Chambers Waters Corporation. Presented by Dr. Diego Rodriguez Cabaleiro Waters Europe Waters Corporation 1

MACHEREY-NAGEL. Chromatography application note. Determination of pyrrolizidine alkaloids. Abstract. Introduction

Edgar Naegele. Abstract

Analysis of Polar Pesticides Using a Mixed-Phase Mode HPLC Column

Extraction of a Comprehensive Steroid Panel from Human Serum Using ISOLUTE. SLE+ Prior to LC/MS-MS Analysis

The Development of LC/MS Methods for Determination of Polar Drugs of Abuse in Biological Samples

Identification of Steroids in Water by Ion Trap LC/MS/MS Application

Supplementary Information. Effects of Perfluorooctanoic Acid on Metabolic Profiles in Brain and Liver of Mouse by a

[ APPLICATION NOTE ] Oasis PRiME HLB Cartridge for Cleanup of Infant Formula Extracts Prior to UPLC-MS/MS Multiresidue Veterinary Drugs Analysis

UCT SELECTRA AQUEOUS C18 HPLC COLUMNS

Analysis of anti-epileptic drugs in human serum using an Agilent Ultivo LC/TQ

Phenomenex roq QuEChERS Kits. Overview. Spinach Facts

Direct Analysis of Urinary Opioids and Metabolites by Mixed-Mode µelution SPE Combined with UPLC/MS/MS for Forensic Toxicology

HPLC Analysis of Sugars

LC-Based Lipidomics Analysis on QTRAP Instruments

Determination of Selected Illegal Drugs and its Important Metabolites in Waste Water by Large Volume Direct Injection HPLC-MS/MS

Application Note. Authors. Abstract. Food

Analysis of HMF by HPLC

Transcription:

Simultaneous Quantitative Analysis of Total Catecholamines and Metanephrines in Urine Using 500 MG CLEAN UP CCX2 and LC-MS/MS UCT Part Numbers: CUCCX256 - Clean-Up CCX2 (C8 + Carboxylic Acid) 500mg/6mL SLPFPP100ID21-3UM - Selectra PFPP HPLC column 100 x 2.1mm, 3um SLPFPPGDC20-3UM - Selectra PFPP guard column 10 x 2.0mm, 3um SLDGRDHLDR Guard cartridge holder June 2015 Dopamine Epinephrine Norepinephrine pka = 9.27 pka = 8.9 pka = 8.85 Metanephrine Normetanephrine pka = 9.25 pka = 9.06 INTRODUCTION Catecholamines are hormones produced by the cells in the interior region of the adrenal glands. These hormones function in the control of heart rate, metabolism and blood pressure (1). The primary catecholamines are dopamine, norepinephrine, and epinephrine. Metanephrine and normetanephrine are the 3-methoxy metabolites of epinephrine and norepinephrine, respectively. Elevated catecholamine levels are commonly associated w ith stress; how ever in patients w ith pheochromocytoma or paragangliomas, these hormones are released into the body w ithout being triggered by any outside factors (2). Pheochromocytoma is a condition in w hich a neuro-endocrine tumor develops in the medulla of the adrenal glands. It originates from the chromaffin cells and results in uncontrolled secretion of epinephrine and other catecholamines. The classic symptoms of pheochromocytomas are those attributable to excess adrenaline

production. Patients often experience episodes of sw eating, headache, hypertension and heart palpitations. Pheochromocytomas are rare and usually benign; how ever, in about 10% of cases, these tumors can be malignant (2). When a tumor of chromaffin cells occurs outside of the adrenal glands it is know n as a paraganglioma. These tumors produce the same effects as pheochromocytomas and can form anyw here in the body. Patients w ho are thought to have a pheochromocytoma are often diagnosed follow ing biochemical tests that measure the levels of catecholamines and metanephrines. Metanephrines are stable metabolites of catecholamines that are co-secreted directly w ith catecholamines from these tumors. While catecholamines only last a short time in the body before they are metabolized, metanephrines last much longer making them a more informative marker to indicate an abnormality (3). Catecholamine and metanephrine levels may be measured in either plasma or in urine that has been collected over a 24 hour period. Generally, plasma tests are preferred due to the enhanced sensitivity of this assay, but there is elevated risk of reporting false positives utilizing this matrix. The 24 hour urine test is considered to be much more conclusive. The criterion used to deem a sample positive for pheochromocytoma is metanephrine values tw ice the average upper limit (1). By utilizing UCT s CLEAN UP CCX extraction columns along w ith a Selectra PFPP HPLC column, excellent sample clean up and analyte separation w as achieved. This w as demonstrated by the observation of good recovery for all five of the hormones analyzed. PROCEDURE 1. Prepare Sample To 1 ml of urine add internal standard(s) and 100 µl of 6M HCl. Incubate for 20 minutes at 90ºC for 20 minutes. Neutralize ph w ith NaOH (~ 75 µl) and 3mL of Acetate buffer (ph ~ 7.0). Mix/Vortex 2. Condition Column 1 x 3 ml MeOH 1 x 3 ml DI H 2 O 1 x 3 ml Acetate Buffer (ph 7) 3. Apply Sample Load at 1 to 2 ml/minute.

4. Wash column 1 x 3 ml DI H 2 O 1 x 3 ml 50:50 MeOH:ACN Dry column under full vacuum or pressure for 10-15 minutes. 5. Elute analytes 1 x 3 ml MeOH w / 5% formic acid Collect eluate at 1-2 ml/ minute. NOTE: A 1% HCl in MeOH solution has been used to prevent volatilization by the formation of the hydrochloric salt of the drugs. 6. Dry eluate Evaporate to dryness at < 40 C. 7. Reconstitute Reconstitute sample in 100 μl of mobile phase. LC-MS/MS METHOD: 2 4 1 3 5 Chromatogram -- Catecholamine Standard 100ng/mL

MRM Transitions Analyte Retention Time (min) Q1 Q3 1. Norepinephrine 1.19 170.4 152.0 2. Epinephrine 1.45 184.0 166.0 3. Normetanephrine 1.85 166.9 135.0 4. Dopamine 2.12 153.9 136.9 5. Metanephrine 3.12 180.0 165.0 Instrument Agilent 1200 Binary Pump SL Detector AB Sciex API 4000 QTrap MS/MS Column UCT Selectra PFPP column, 100 x 2.1 mm, 3 μm Guard Column UCT Selectra PFPP, 10 x 2.0 mm, 3 μm Column Temperature 50 C Flow Rate 0.3 ml/min Injection Volume 10 µl Gradient Program: Time (min) % Mobile Phase A (0.1% FA in w ater) % Mobile Phase B (0.1% FA in Methanol) 0 99 1 2 99 1 3 0 100 5 0 100 5.2 99 1 10 99 1

RESULTS: Recovery (n= 3) Analyte 75 ng/ml 500 ng/ml 2000 ng/ml Epinephrine 86% 88% 84% Norepinephrine 101% 91% 79% Metanephrine 79% 78% 63% Normetanephrine 49% 42% 34% Dopamine 97% 91% 86% DISCUSSION: The structures and pka values of epinephrine, norepinephrine, metanephrine, normetanephrine and dopamine make them ideal candidates for clean-up via cation exchange solid phase extraction (SPE). Tw o chemically different SPE columns w ith various combinations of w ash and elution solvents w ere evaluated for the optimization of this procedure. UCT s benzenesulfonic acid strong cation exchange column and corresponding methodology allow ed for excellent recovery of the metanephrines, how ever, it greatly reduced the recovery of the catecholamines regardless of the w ash/elution solvent combination. Previous literature suggests that the use of highly basic elution solvents containing ammonium hydroxide lead to degradation of the catecholamines, w hich w as noted in the extraction results. In an attempt to improve recovery, a 2% trimethylamine / 98% methanol solution w as substituted for elution purposes and no improvement w as noted. Subsequently, UCT s CLEAN UP CCX w as selected. This is a carboxylic acid, w eak cation exchange, sorbent. It allow ed for adequate recovery of the metanephrines w ithout compromising the stability of the catecholamines. Samples w ere loaded at ph 7, ensuring that the functional groups of both the analytes of interest and the sorbent w ere fully charged. The charged state allow ed for strong ionic interactions betw een the sorbent and the catecholamines. The ionic interaction permitted the use of an extensive range of w ash solutions. Ultimately, it w as determined that a D.I. H 2 O w ash follow ed by an acetonitrile: methanol (50:50) w ash best removed unw anted matrix and other endogenous interferences. For elution purposes, an acidic solution (5% formic acid in methanol) sufficiently low ered the ph of the sorbent. This neutralized the carboxylic acid groups on the sorbent and disrupted the ionic bonds w ith the analytes of interest. The analytes w ere now able to be efficiently removed from the SPE column. Prior to evaporating to dryness, 100 µl of a 1% HCl in methanol solution w as added to the diluent to prevent volatilization of the analytes.

CONCLUSIONS: 1. Both catecholamine and metanephrine levels need to be monitored. This is done for both the diagnosis of a patient w ith pheochromocytoma, and also to monitor treatment for patients w ho are already know n to have the condition. 2. By utilizing UCT s CLEAN UP CCX extraction columns and corresponding methodology, total urine catecholamine and metanephrine levels can be monitored simultaneously, reducing both analyst time and instrument time. 3. UCT s PFPP analytical column allow ed for the simultaneous separation of the extremely polar catecholamines and metanephrines. Of the various HPLC phases tried (pentafluorophenylpropyl, polyaromatic, aqueous C18, and Diol) and conditions attempted, the Selectra PFPP (pentafluorophenylpropyl) column w as the only one that produced acceptable baseline separation and peak shape for the quantitation of all analytes. 4. It is strongly recommended to use matrix-matched calibration curves, w hich include isotopically labeled internal standards to compensate for any remaining matrix that is not removed via the extraction procedure. REFERENCES: 1. " Catecholamines in Urine." WebMD. WebMD, 20 June 2012. Web. 15 June 2015. 2. " Pheochromocytoma: MedlinePlus Medical Encyclopedia." U.S National Library of Medicine. U.S. National Library of Medicine, 15 June 2015. Web. 16 June 2015. 3. " Pheochromocytoma." - Mayo Clinic. N.p., 02 May 2014. Web. 22 June 2015. 5106-03-01 UCT, LLC 2731 Bartram Road Bristol, PA 19007 800.385.3153 215.781.9255 www.unitedchem.com Email: methods@unitedchem.com UCT, LLC 2015 All rights reserved