000020489 001__ 20489 000020489 005__ 20180208220755.0 000020489 0247_ $$2pmid$$apmid:22451051 000020489 0247_ $$2DOI$$a10.1002/elps.201100381 000020489 0247_ $$2WOS$$aWOS:000302010700007 000020489 037__ $$aPreJuSER-20489 000020489 041__ $$aeng 000020489 082__ $$a570 000020489 084__ $$2WoS$$aBiochemical Research Methods 000020489 084__ $$2WoS$$aChemistry, Analytical 000020489 1001_ $$0P:(DE-Juel1)VDB94855$$aPosch, T.N.$$b0$$uFZJ 000020489 245__ $$aImplementation of a design of experiments to study the influence of the background electrolyte on separation and detection in non-aqueous capillary electrophoresis-mass spectrometry 000020489 260__ $$aWeinheim$$bWiley-Blackwell$$c2012 000020489 300__ $$a583 - 598 000020489 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article 000020489 3367_ $$2DataCite$$aOutput Types/Journal article 000020489 3367_ $$00$$2EndNote$$aJournal Article 000020489 3367_ $$2BibTeX$$aARTICLE 000020489 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000020489 3367_ $$2DRIVER$$aarticle 000020489 440_0 $$01792$$aElectrophoresis$$v33$$x0173-0835$$y4 000020489 500__ $$3POF3_Assignment on 2016-02-29 000020489 500__ $$aThe help of Jorg Roscher is gratefully acknowledged. We thank the Helmholtz Initiative and Networking Fund for financial support. 000020489 520__ $$aNon-aqueous capillary electrophoresis (NACE) background electrolytes are most often composed of a mixture of methanol and acetonitrile (ACN) with soluble ammonium salts added as electrolyte. In this study on NACE-MS, we used a mixture of glacial acetic acid and ACN giving rise to an acidic background electrolyte (BGE) with a very low dielectric constant. Impressive changes in selectivity and resolution were observed for structurally closely related indole alkaloids including diastereomers upon addition of ammonium formate as electrolyte and upon variation of the solvent ratio. In order to obtain best separation and MS detection conditions and to reveal the influence of the parameters of the BGE on separation and detection and vice versa of the MS parameters on separation, an optimization strategy was employed using a design of experiments in a central composite design with response surface methodology. It was proven that at high electroosmotic flow conditions capillary electrophoretic separations and thus optimization can be realized without interference from the coupling to an MS system. Several significantly interacting parameters were revealed, which are not accessible with classical univariate optimization approaches. With this optimization, alkaloid mixtures from a plant extract of Mitragyna speciosa, containing a large number of diastereomeric compounds were successfully separated. 000020489 536__ $$0G:(DE-Juel1)FUEK506$$2G:(DE-HGF)$$aTechniken, Innovation und Gesellschaft (TIG)$$cP47$$x0 000020489 588__ $$aDataset connected to Web of Science, Pubmed 000020489 65320 $$2Author$$aDesign of experiments 000020489 65320 $$2Author$$aHeteroconjugation 000020489 65320 $$2Author$$aIndole alkaloids 000020489 65320 $$2Author$$aIon-pairing 000020489 65320 $$2Author$$aNon-aqueous capillary electrophoresis 000020489 650_2 $$2MeSH$$aAcetic Acid: chemistry 000020489 650_2 $$2MeSH$$aAcetonitriles: chemistry 000020489 650_2 $$2MeSH$$aAnalysis of Variance 000020489 650_2 $$2MeSH$$aElectrolytes: chemistry 000020489 650_2 $$2MeSH$$aElectrophoresis, Capillary: methods 000020489 650_2 $$2MeSH$$aIndole Alkaloids: analysis 000020489 650_2 $$2MeSH$$aIndole Alkaloids: isolation & purification 000020489 650_2 $$2MeSH$$aMass Spectrometry: methods 000020489 650_2 $$2MeSH$$aMitragyna: chemistry 000020489 650_2 $$2MeSH$$aModels, Chemical 000020489 650_2 $$2MeSH$$aPlant Extracts: chemistry 000020489 650_2 $$2MeSH$$aResearch Design 000020489 650_7 $$00$$2NLM Chemicals$$aAcetonitriles 000020489 650_7 $$00$$2NLM Chemicals$$aElectrolytes 000020489 650_7 $$00$$2NLM Chemicals$$aIndole Alkaloids 000020489 650_7 $$00$$2NLM Chemicals$$aPlant Extracts 000020489 650_7 $$064-19-7$$2NLM Chemicals$$aAcetic Acid 000020489 650_7 $$075-05-8$$2NLM Chemicals$$aacetonitrile 000020489 650_7 $$2WoSType$$aJ 000020489 7001_ $$0P:(DE-HGF)0$$aMüller, A.$$b1 000020489 7001_ $$0P:(DE-HGF)0$$aSchulz, W.$$b2 000020489 7001_ $$0P:(DE-HGF)0$$aPütz, M.$$b3 000020489 7001_ $$0P:(DE-Juel1)VDB93008$$aHuhn, C.$$b4$$uFZJ 000020489 773__ $$0PERI:(DE-600)1475486-1$$a10.1002/elps.201100381$$gVol. 33, p. 583 - 598$$p583 - 598$$q33<583 - 598$$tElectrophoresis$$v33$$x0173-0835$$y2012 000020489 8567_ $$uhttp://dx.doi.org/10.1002/elps.201100381 000020489 909CO $$ooai:juser.fz-juelich.de:20489$$pVDB 000020489 9141_ $$y2012 000020489 915__ $$0StatID:(DE-HGF)0010$$2StatID$$aJCR/ISI refereed 000020489 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR 000020489 915__ $$0StatID:(DE-HGF)0110$$2StatID$$aWoS$$bScience Citation Index 000020489 915__ $$0StatID:(DE-HGF)0111$$2StatID$$aWoS$$bScience Citation Index Expanded 000020489 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection 000020489 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bThomson Reuters Master Journal List 000020489 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS 000020489 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline 000020489 915__ $$0StatID:(DE-HGF)0310$$2StatID$$aDBCoverage$$bNCBI Molecular Biology Database 000020489 915__ $$0StatID:(DE-HGF)0420$$2StatID$$aNationallizenz 000020489 915__ $$0StatID:(DE-HGF)1030$$2StatID$$aDBCoverage$$bCurrent Contents - Life Sciences 000020489 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews 000020489 9131_ $$0G:(DE-Juel1)FUEK506$$1G:(DE-HGF)POF2-470$$2G:(DE-HGF)POF2-100$$bSchlüsseltechnologien$$kP47$$lTechnologien, Innovationen und Gesellschaft$$vTechniken, Innovation und Gesellschaft (TIG)$$x0$$zvormals P26 000020489 9132_ $$0G:(DE-HGF)POF3-159H$$1G:(DE-HGF)POF3-150$$2G:(DE-HGF)POF3-100$$aDE-HGF$$bForschungsbereich Energie$$lTechnologie, Innovation und Gesellschaft$$vAddenda$$x0 000020489 9201_ $$0I:(DE-Juel1)ZCH-20090406$$gZCH$$kZCH$$lZentralabteilung für Chemische Analysen$$x0 000020489 970__ $$aVDB:(DE-Juel1)136037 000020489 980__ $$aVDB 000020489 980__ $$aConvertedRecord 000020489 980__ $$ajournal 000020489 980__ $$aI:(DE-Juel1)ZEA-3-20090406 000020489 980__ $$aUNRESTRICTED 000020489 981__ $$aI:(DE-Juel1)ZEA-3-20090406 000020489 981__ $$aI:(DE-Juel1)ZCH-20090406