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Publicação:
A trade off between separation, detection and sustainability in liquid chromatographic fingerprinting

dc.contributor.authorFunari, Cristiano S.
dc.contributor.authorCarneiro, Renato L.
dc.contributor.authorCavalheiro, AlbertoJ. [UNESP]
dc.contributor.authorHilder, Emily F.
dc.contributor.institutionUniv Tasmania
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:08:40Z
dc.date.available2014-12-03T13:08:40Z
dc.date.issued2014-08-08
dc.description.abstractIt is now recognized that analytical chemistry must also be a target for green principles, in particular chromatographic methods which typically use relatively large volumes of hazardous organic solvents. More generally, high performance liquid chromatography (HPLC) is employed routinely for quality control of complex mixtures in various industries. Acetonitrile and methanol are the most commonly used organic solvents in HPLC, but they generate an impact on the environment and can have a negative effect on the health of analysts. Ethanol offers an exciting alternative as a less toxic, biodegradable solvent for HPLC. In this work we demonstrate that replacement of acetonitrile with ethanol as the organic modifier for HPLC can be achieved without significantly compromising analytical performance. This general approach is demonstrated through the specific example analysis of a complex plant extract. A benchmark method employing acetonitrile for the analysis of Bidens pilosa extract was statistically optimized using the Green Chromatographic Fingerprinting Response (GCFR) which includes factors relating to separation performance and environmental parameters. Methods employing ethanol at 30 and 80 C were developed and compared with the reference method regarding their performance of separation (GCFR) as well as by a new metric, Comprehensive Metric to Compare Liquid Chromatography Methods (CM). The fingerprint with ethanol at 80 C was similar to or better than that with MeCN according to GCFR and CM. This demonstrates that temperature may be used to replace harmful solvents with greener ones in HPLC, including for solvents with significantly different physiochemical properties and without loss in separation performance. This work offers a general approach for the chromatographic analysis of complex samples without compromising green analytical chemistry principles. (C) 2014 Published by Elsevier B.V.en
dc.description.affiliationUniv Tasmania, Australian Ctr Res Separat Sci ACROSS, Sch Phys Sci, Hobart, Tas 7001, Australia
dc.description.affiliationUniv Fed Sao Carlos, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipAustralian Research Council (ARC)
dc.description.sponsorshipARC Future Fellowship
dc.description.sponsorshipIdARC Future FellowshipFT0990521
dc.description.sponsorshipIdFAPESP: 12/15877-7
dc.format.extent34-42
dc.identifierhttp://dx.doi.org/10.1016/j.chroma.2014.05.018
dc.identifier.citationJournal Of Chromatography A. Amsterdam: Elsevier Science Bv, v. 1354, p. 34-42, 2014.
dc.identifier.doi10.1016/j.chroma.2014.05.018
dc.identifier.issn0021-9673
dc.identifier.urihttp://hdl.handle.net/11449/111454
dc.identifier.wosWOS:000339144000005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Chromatography A
dc.relation.ispartofjcr3.716
dc.relation.ispartofsjr1,378
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectGreen chromatographyen
dc.subjectGreen solventsen
dc.subjectSolvent replacementen
dc.subjectHigh temperature liquid chromatographyen
dc.subjectGreen metabolite profilingen
dc.titleA trade off between separation, detection and sustainability in liquid chromatographic fingerprintingen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes2518006820764120[3]
unesp.author.orcid0000-0001-8214-9957[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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