Improved plasma free metadrenaline analysis requires mixed mode cation exchange solid-phase extraction prior to liquid chromatography tandem mass spectrometry detection
The investigation and effective management of phaeochromocytoma involves biochemical measurement of either conjugated total urine or plasma free metadrenalines. Current analytical methods include enzyme-linked immunosorbent assays, high-performance liquid chromatography (HPLC) with electrochemical d...
Saved in:
Published in | Annals of clinical biochemistry Vol. 48; no. Pt 4; p. 352 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
01.07.2011
|
Subjects | |
Online Access | Get more information |
ISSN | 1758-1001 |
DOI | 10.1258/acb.2011.010235 |
Cover
Abstract | The investigation and effective management of phaeochromocytoma involves biochemical measurement of either conjugated total urine or plasma free metadrenalines. Current analytical methods include enzyme-linked immunosorbent assays, high-performance liquid chromatography (HPLC) with electrochemical detection (ECD) or liquid chromatography tandem mass spectrometry (LCMS/MS). Since the first two methods are either extremely laborious, necessitate low sample run numbers, result in slow turnaround times or are subject to analytical interference, a robust, routine clinical method is not achievable. We established a novel sample preparation method to measure plasma free metadrenalines using LCMS/MS.
Three different solid-phase extraction (SPE) methods were compared: hydrophilic-lipophilic balance sorbent (HLB), weak cation exchange (WCX) and mixed mode cation exchange (MCX) and their ability to remove interfering compounds prior to LCMS/MS analysis. Maximum recovery of plasma free metadrenaline and plasma free normetadrenaline were achieved by positively charging compounds prior to SPE application.
Compared with HLB and WCX cartridges, MCX extraction resulted in chromatography without co-eluting interference with superior assay precision and accuracy. Additionally, samples that could not be quantified because of interference using HPLC/ECD could be readily assayed using this new method.
The use of the MCX SPE method with LCMS/MS detection provides an improved assay to measure plasma free metadrenalines in comparison to many available alternative methods. |
---|---|
AbstractList | The investigation and effective management of phaeochromocytoma involves biochemical measurement of either conjugated total urine or plasma free metadrenalines. Current analytical methods include enzyme-linked immunosorbent assays, high-performance liquid chromatography (HPLC) with electrochemical detection (ECD) or liquid chromatography tandem mass spectrometry (LCMS/MS). Since the first two methods are either extremely laborious, necessitate low sample run numbers, result in slow turnaround times or are subject to analytical interference, a robust, routine clinical method is not achievable. We established a novel sample preparation method to measure plasma free metadrenalines using LCMS/MS.
Three different solid-phase extraction (SPE) methods were compared: hydrophilic-lipophilic balance sorbent (HLB), weak cation exchange (WCX) and mixed mode cation exchange (MCX) and their ability to remove interfering compounds prior to LCMS/MS analysis. Maximum recovery of plasma free metadrenaline and plasma free normetadrenaline were achieved by positively charging compounds prior to SPE application.
Compared with HLB and WCX cartridges, MCX extraction resulted in chromatography without co-eluting interference with superior assay precision and accuracy. Additionally, samples that could not be quantified because of interference using HPLC/ECD could be readily assayed using this new method.
The use of the MCX SPE method with LCMS/MS detection provides an improved assay to measure plasma free metadrenalines in comparison to many available alternative methods. |
Author | Cooke, Brian Glendenning, Paul Clarke, Michael W Hoad, Kirsten |
Author_xml | – sequence: 1 givenname: Michael W surname: Clarke fullname: Clarke, Michael W email: michael.clarke@uwa.edu.au organization: Department of Core Clinical Pathology and Biochemistry, Royal Perth Hospital, Perth, Western Australia, Australia. michael.clarke@uwa.edu.au – sequence: 2 givenname: Brian surname: Cooke fullname: Cooke, Brian – sequence: 3 givenname: Kirsten surname: Hoad fullname: Hoad, Kirsten – sequence: 4 givenname: Paul surname: Glendenning fullname: Glendenning, Paul |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21690275$$D View this record in MEDLINE/PubMed |
BookMark | eNo1kM1OwzAQhC0EorRw5ob8Aim2EyfNEVX8VKrEBc7Vxt40RnEcbBc1b8RjYhU4zWpG-2k0c3I-uAEJueVsyYVc3YNqloJxvmSciVyekSteyVXGGeMzMg_hgzEmKsYuyUzwsk63vCLfGzt694Wajj0EC7T1iNRiBO1xgN4MSCHpFEygHj8PxmOg1hzTh3UaqYJo3EDxqDoY9kiD643Oxg4CJjN6UKd89MZ5Gh3tTWJoqjrvLES39zB2E40waLTUQgg0jKhiSjH6iWqMeCJck4sW-oA3f7og70-Pb-uXbPv6vFk_bDOVV0XM2oZzaJqyrJXUgNiolZCsLrhGmYsKGasU16JMUygo61xWbdHWZcmLBvOmBrEgd7_c8dBY1LtU3IKfdv-TiR8LfnQJ |
CitedBy_id | crossref_primary_10_1016_j_cca_2019_05_024 crossref_primary_10_3390_nu8090565 crossref_primary_10_1177_0004563218774590 crossref_primary_10_1258_acb_2012_012112 crossref_primary_10_1373_clinchem_2014_233551 crossref_primary_10_1016_j_clinbiochem_2016_01_010 |
ContentType | Journal Article |
DBID | CGR CUY CVF ECM EIF NPM |
DOI | 10.1258/acb.2011.010235 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | no_fulltext_linktorsrc |
Discipline | Medicine Chemistry |
EISSN | 1758-1001 |
ExternalDocumentID | 21690275 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- .55 .GJ 0R~ 23M 35A 36B 4.4 53G 5GY 5I- 5I. 5RE 5VS 6J9 7X7 88E 88I 8AF 8AO 8CJ 8FE 8FG 8FH 8FI 8FJ 8R4 8R5 AACMV AACTG AAEWN AAGMC AAJIQ AAJOX AAKGS AAQXH AATBZ AAUAS AAWTL AAXOT AAXTJ AAYTG AAZBJ ABDWY ABHKI ABJCF ABJIS ABLUO ABPGX ABUJY ABUWG ABVVC ABWRX ACFEJ ACFIC ACFMA ACFYK ACGBL ACGFO ACGFS ACGOD ACGZN ACGZU ACIWK ACJOP ACJTF ACLFY ACLHI ACPRK ACUAV ACXMB ADBBV ADMPF ADNBR ADTBJ ADWAY AECGH AECVZ AEDTQ AEKYL AEMJX AENEX AEPTA AEWDL AEWLI AEXFG AFEGE AFIEG AFKRA AFKRG AFNTS AGHKR AGPXR AGWFA AHDMH AHMBA AHOKE AI. AIGRN AIIQI AJABX AJEFB AJMMQ AJSCY AJUZI AJXAJ ALIPV ALKWR ALMA_UNASSIGNED_HOLDINGS ALTZF AMCVQ AOSDY ARTOV AYAKG AZQEC BBNVY BBRGL BENPR BES BGLVJ BHPHI BKIIM BPACV BPHCQ BVXVI BWJAD CAG CCPQU CGR COF CORYS CQQTX CS3 CUTAK CUY CVF D1I D1J DB0 DC. DC0 DD- DE- DF0 DN0 DO- DWQXO EBS ECM EIF EJD EMOBN F5P FHBDP FYUFA GNUQQ H13 HCIFZ HMCUK HZ~ J5H J8X KB. LK8 M1P M2P M2Q M4V M7P MV1 NPM O9- P.B P.C P2P PDBOC PHGZT PQQKQ PROAC PSQYO Q1R Q2X ROL RWL RXW S0X SAUOL SCNPE SFC SHG SPQ SPV TAE TRM UCJ UKHRP VH1 WH7 X6Y X7M ZXP |
ID | FETCH-LOGICAL-c374t-fb11abb669c5daeebc8250941de5327e007c1d26002ca69357f4f96614be3b9a2 |
IngestDate | Thu Apr 03 06:53:16 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | Pt 4 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c374t-fb11abb669c5daeebc8250941de5327e007c1d26002ca69357f4f96614be3b9a2 |
OpenAccessLink | https://journals.sagepub.com/doi/pdf/10.1258/acb.2011.010235 |
PMID | 21690275 |
ParticipantIDs | pubmed_primary_21690275 |
PublicationCentury | 2000 |
PublicationDate | 2011-Jul |
PublicationDateYYYYMMDD | 2011-07-01 |
PublicationDate_xml | – month: 07 year: 2011 text: 2011-Jul |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Annals of clinical biochemistry |
PublicationTitleAlternate | Ann Clin Biochem |
PublicationYear | 2011 |
SSID | ssj0002700 |
Score | 1.958258 |
Snippet | The investigation and effective management of phaeochromocytoma involves biochemical measurement of either conjugated total urine or plasma free... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | 352 |
SubjectTerms | Adrenal Gland Neoplasms - blood Adrenal Gland Neoplasms - diagnosis Analytic Sample Preparation Methods Cation Exchange Resins - chemistry Chromatography, Liquid - methods Humans Metanephrine - blood Normetanephrine - blood Pheochromocytoma - blood Pheochromocytoma - diagnosis Solid Phase Microextraction - methods Tandem Mass Spectrometry - methods |
Title | Improved plasma free metadrenaline analysis requires mixed mode cation exchange solid-phase extraction prior to liquid chromatography tandem mass spectrometry detection |
URI | https://www.ncbi.nlm.nih.gov/pubmed/21690275 |
Volume | 48 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnZ1Nb9NAEIZXKUjQC4IC5Vtz4LYy1I6_coQKiECtOLRSb9V-jFVLTRwZVyr8Iv4S_4aZ3XXspiAVLlZkx5aVebL7ej3zjhCvY1PO9lBXURwbE6U2xqgkHRHR1Kdohrdau2z3g8N8fpx-PslOJpNfo6yli06_MT_-WFfyP1GlfRRXrpL9h8iuL0o76DPFl7YUYdreKMZ-RYAk44o08ELJqkXkntCKy7OVE5CqNx1pkXN-8Ztc1Jd0BnfAkX65TuKlL_-VdLe1jVZnNLPRzq4NfcRXbc25iI08r-kaVpqztiGhG8yuJS9G4EIuSIZLV7jJDghd-11a7Fyi13KsgAfH5nVRpq65bZfvO3c9bygk9svBGLh3CX3fjtieNx7WLzXp2aG-7dO56_G7DK1b1omQdli5LfqFDvSDMz3bROwZNR6903JE6ddOpqPReOrNca_NEknGlQ_K6GDhyvYV2fibFObVwkGT8GvEpLjB0Q3b7v7QltgqCp4xDnkZKUgEftsffKboXt5u3IkzqPZnbzzsONFzdF_cC08r8M6j90BMcLkj7u73wdoRdw5CbsZD8bOnETyNwDTCFRqhpxF6GsHRCEwjeBqhpxFGNMJAIzgaoWvA0whXaQRPIzCNMKYR1jQ-EscfPxztz6PQByQy0yLtokrHsaJBI5-ZzCpEbcqEfR9ji9k0KZBkroktd1pIjMpn06yo0mrGwlPjVM9U8ljcWjZLfCKgwlgZleWm0pgqs6dIkWOaW10kWFaZfSp2_e99uvJmL6d9JJ799chzsT3g-kLcruhfhC9Jqnb6lQv7b8KsoVI |
linkProvider | National Library of Medicine |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Improved+plasma+free+metadrenaline+analysis+requires+mixed+mode+cation+exchange+solid-phase+extraction+prior+to+liquid+chromatography+tandem+mass+spectrometry+detection&rft.jtitle=Annals+of+clinical+biochemistry&rft.au=Clarke%2C+Michael+W&rft.au=Cooke%2C+Brian&rft.au=Hoad%2C+Kirsten&rft.au=Glendenning%2C+Paul&rft.date=2011-07-01&rft.eissn=1758-1001&rft.volume=48&rft.issue=Pt+4&rft.spage=352&rft_id=info:doi/10.1258%2Facb.2011.010235&rft_id=info%3Apmid%2F21690275&rft_id=info%3Apmid%2F21690275&rft.externalDocID=21690275 |