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Title: High performance liquid chromatography analysis of 2-mercaptoethylamine (cysteamine) in biological samples by derivatization with N-(1-pyrenyl) maleimide (NPM) using fluorescence detection
Author (s): Ogony, J.
Mare, S.
Wu, W.
Ercal, Nuran
Department/Lab Affiliations: Chemistry
Environmental Research Center
Keywords: 2-Mercaptoethylamine.
CSH.
Cysteamine.
NPM.
Subject Terms: Cystinosis.
High performance liquid chromatography.
Oxidative stress.
Thiols.
Issue Date: 2006
Publisher: Elsevier
Citation: Ogony, J., Mare, S., Wu, W., and Ercal, N. “High Performance Liquid Chromatography Analysis of 2-Mercaptoethylamine (Cysteamine) in Biological Samples by Derivatization with N-(1-pyrenyl) maleimide (NPM) using Fluorescence Detection,” Biomedical Chromatography,Volume 843, Issue 1, 20 October 2006, Pages 57-62 2006.
Abstract: 2-Mercaptoethylamine (cysteamine) is an aminothiol compound used as a drug for the treatment of cystinosis, an autosomal recessive lysosomal storage disorder. Because of cysteamine's important role in clinical settings, its analysis by sensitive techniques has become pivotal. Unfortunately, the available methods are either complex or labor intensive. Therefore, we have developed a new rapid, sensitive, and simple method for determining cysteamine in biological samples (brain, kidney, liver, and plasma), using N-(1-pyrenyl) maleimide (NPM) as the derivatizing agent and reversed-phase high performance liquid chromatography (HPLC) with a fluorescence detection method (λex = 330 nm, λem = 376 nm). The mobile phase was acetonitrile and water (70:30) with acetic acid and o-phosphoric acid (1 mL/L). The calibration curve for cysteamine in serine borate buffer (SBB) was found to be linear over a range of 0–1200 nM (r2 = 0.9993), and in plasma and liver matrix, the r2 values were 0.9968 and 0.9965, respectively. The coefficients of the variation for the within-run and between-run precisions ranged from 0.68 to 9.90% and 0.63 to 4.17%, respectively. The percentage of relative recovery ranged from 94.1 to 98.6%.
Type: Article - Journal
text
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titleHigh performance liquid chromatography analysis of 2-mercaptoethylamine (cysteamine) in biological samples by derivatization with N-(1-pyrenyl) maleimide (NPM) using fluorescence detection
contributor.authorOgony, J.
contributor.authorMare, S.
contributor.authorWu, W.
contributor.authorErcal, Nuran
contributor.deptlabChemistry
contributor.deptlabEnvironmental Research Center
subject2-Mercaptoethylamine.
subjectCSH.
subjectCysteamine.
subjectNPM.
subject.LCSHCystinosis.
subject.LCSHHigh performance liquid chromatography.
subject.LCSHOxidative stress.
subject.LCSHThiols.
date.issued2006
publisherElsevier
identifier.citationOgony, J., Mare, S., Wu, W., and Ercal, N. “High Performance Liquid Chromatography Analysis of 2-Mercaptoethylamine (Cysteamine) in Biological Samples by Derivatization with N-(1-pyrenyl) maleimide (NPM) using Fluorescence Detection,” Biomedical Chromatography,Volume 843, Issue 1, 20 October 2006, Pages 57-62 2006.
identifier.pub.URI
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6X0P-4K7FJHK-3&_user=1036314&_coverDate=10%2F20%2F2006&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050731&_version=1&_urlVersion=0&_userid=1036314&md5=6911c3102b3303c63619d4e05ff4ed9a
description.abstract2-Mercaptoethylamine (cysteamine) is an aminothiol compound used as a drug for the treatment of cystinosis, an autosomal recessive lysosomal storage disorder. Because of cysteamine's important role in clinical settings, its analysis by sensitive techniques has become pivotal. Unfortunately, the available methods are either complex or labor intensive. Therefore, we have developed a new rapid, sensitive, and simple method for determining cysteamine in biological samples (brain, kidney, liver, and plasma), using N-(1-pyrenyl) maleimide (NPM) as the derivatizing agent and reversed-phase high performance liquid chromatography (HPLC) with a fluorescence detection method (λex = 330 nm, λem = 376 nm). The mobile phase was acetonitrile and water (70:30) with acetic acid and o-phosphoric acid (1 mL/L). The calibration curve for cysteamine in serine borate buffer (SBB) was found to be linear over a range of 0–1200 nM (r2 = 0.9993), and in plasma and liver matrix, the r2 values were 0.9968 and 0.9965, respectively. The coefficients of the variation for the within-run and between-run precisions ranged from 0.68 to 9.90% and 0.63 to 4.17%, respectively. The percentage of relative recovery ranged from 94.1 to 98.6%.
typeArticle - Journal
type.DCMITypetext
type.statusFinal version
rightsThis material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All persons copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.
rights.URI
http://www.elsevier.com/wps/find/authorsview.authors/authorsrights
date.accessioned2007-04-11T17:00:48Z
date.available2007-12-17T20:47:59Z
identifier.persist.URI
http://scholarsmine.mst.edu/post_prints/HighPerformanceLiquidChromatography_09007dcc8042c377.html