{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T21:31:08Z","timestamp":1791927068073,"version":"4.3.4"},"reference-count":35,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2012,6,28]],"date-time":"2012-06-28T00:00:00Z","timestamp":1340841600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Electrophoresis"],"published-print":{"date-parts":[[2012,7]]},"abstract":"<jats:p>Asymmetric dimethylarginine (<jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content>) is an inhibitor of nitric oxide synthase and a risk factor for cardiovascular events. We have developed a new derivatization method to enable baseline separation of the regio\u2010isomers, <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content>, and symmetric dimethylarginine (<jats:styled-content style=\"fixed-case\">SDMA<\/jats:styled-content>), within 15 min on a <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>18 reverse phase column. Reacting naphthalene\u20102,3\u2010dicarboxaldehyde with <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SDMA<\/jats:styled-content> in the presence of 2\u2010mercaptoethanol produces corresponding 2,3\u2010dihydro\u2010benzo[f]isoindol\u20101\u2010ones that are more stable than previously reported ortho\u2010phthaldialdehyde and 2\u2010mercaptoethanol derivatives. <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content> quantitation of these derivatives can be used to determine <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SDMA<\/jats:styled-content> concentrations in the plasma of patients to receive on\u2010pump coronary artery bypass grafting <jats:styled-content style=\"fixed-case\">(CABG)<\/jats:styled-content> surgery. The LOD, LOQ and lower LOQ (LLOQ) of this method were determined to be 2.6, 8.7, and 25 nM for <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content>, and 2.5, 8.3, and 25 nM for <jats:styled-content style=\"fixed-case\">SDMA<\/jats:styled-content>, respectively, with consumption of only 50 \u03bcL of plasma. The relative standard deviations and relative errors of the intraday and interday determinations, as measurements of reproducibility and accuracy, are all within 15%. The <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SDMA<\/jats:styled-content> concentrations in patient plasma are 298.1 \u00b1 11.2 nM (mean \u00b1 <jats:styled-content style=\"fixed-case\">S.E.M.<\/jats:styled-content>, <jats:italic>n<\/jats:italic> = 123) and 457.7 \u00b1 19.8 nM (mean \u00b1 <jats:styled-content style=\"fixed-case\">S.E.M.<\/jats:styled-content>, <jats:italic>n<\/jats:italic> = 123), respectively. Upon unblinding of our clinical trial, these predetermined values might explain patient clinical outcomes associated with on\u2010pump <jats:styled-content style=\"fixed-case\">CABG<\/jats:styled-content> surgery, as <jats:styled-content style=\"fixed-case\">ADMA<\/jats:styled-content> is known to inhibit nitric oxide production. Furthermore, this derivatization reaction in conjunction with <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content> analysis may open a venue to explore alternative chemical labeling modes for <jats:styled-content style=\"fixed-case\">LC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MS<\/jats:styled-content> applications, such as analysis of other amino acids, metabolites, and peptides containing primary amine group(s).<\/jats:p>","DOI":"10.1002\/elps.201100536","type":"journal-article","created":{"date-parts":[[2012,6,28]],"date-time":"2012-06-28T07:26:45Z","timestamp":1340868405000},"page":"1911-1920","source":"Crossref","is-referenced-by-count":12,"title":["A new derivatization method coupled with <scp>LC<\/scp>\u2010<scp>MS<\/scp>\/<scp>MS<\/scp> to enable baseline separation and quantification of dimethylarginines in human plasma from patients to receive on\u2010pump <scp>CABG<\/scp> surgery"],"prefix":"10.1002","volume":"33","author":[{"given":"Yu","family":"Hui","sequence":"first","affiliation":[{"name":"Department of Chemistry University of British Colombia  Vancouver BC Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael","family":"Wong","sequence":"additional","affiliation":[{"name":"Department of Chemistry University of British Colombia  Vancouver BC Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joo\u2010oll","family":"Kim","sequence":"additional","affiliation":[{"name":"Department of Chemistry University of British Colombia  Vancouver BC Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer","family":"Love","sequence":"additional","affiliation":[{"name":"Department of Chemistry University of British Colombia  Vancouver BC Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David M.","family":"Ansley","sequence":"additional","affiliation":[{"name":"Department of Anesthesia, Pharmacology, and Therapeutics University of British Columbia  Vancouver BC Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David D.Y.","family":"Chen","sequence":"additional","affiliation":[{"name":"Department of Chemistry University of British Colombia  Vancouver BC 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