Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8023
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dc.contributor.authorMagiera, S.-
dc.contributor.authorGülmez, Şefika-
dc.contributor.authorMichalik, A.-
dc.contributor.authorBaranowska, I.-
dc.date.accessioned2019-08-16T12:34:28Z
dc.date.available2019-08-16T12:34:28Z
dc.date.issued2013-
dc.identifier.issn0021-9673-
dc.identifier.urihttps://hdl.handle.net/11499/8023-
dc.identifier.urihttps://doi.org/10.1016/j.chroma.2013.06.047-
dc.description.abstractA new approach based on microextraction by packed sorbent (MEPS) and a reversed-phase ultra-high pressure liquid chromatography (UHPLC) method was developed and validated for the determination and quantification of nonsteroidal anti-inflammatory drugs (NSAIDs) (acetylsalicylic acid, ketoprofen, diclofenac, naproxen and ibuprofen) in human urine. The important factors that could influence the extraction were previously screened using the Plackett-Burman design approach. The optimal MEPS extraction conditions were obtained using C18 phase as a sorbent, small sample volume (20µL) and a short time period (approximately 5min) for the entire sample preparation step. The analytes were separated on a core-shell column (Poroshell 120 EC-C18; 100mm×3.0mm; 2.7µm) using a binary mobile phase composed of aqueous 0.1% trifluoroacetic acid and acetonitrile in the gradient elution mode (4.5min of analysis time). The analytical method was fully validated based on linearity, limits of detection (LOD), limits of quantification (LOQ), inter- and intra-day precision and accuracy, and extraction yield. Under optimised conditions, excellent linearity (R2>0.9991), limits of detection (1.07-16.2ngmL-1) and precision (0.503-9.15% RSD) were observed for the target drugs. The average absolute recoveries of the analysed compounds extracted from the urine samples were 89.4-107%. The proposed method was also applied to the analysis of NSAIDs in human urine. The new approach offers an attractive alternative for the analysis of selected drugs from urine samples, providing several advantages including fewer sample preparation steps, faster sample throughput and ease of performance compared to traditional methodologies. © 2013 Elsevier B.V.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Chromatography Aen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMicroextraction by packed sorbenten_US
dc.subjectNonsteroidal anti-inflammatory drugsen_US
dc.subjectPlackett-Burman designen_US
dc.subjectUltra-high pressure liquid chromatographyen_US
dc.subjectGradient elution modeen_US
dc.subjectLimits of quantificationen_US
dc.subjectMicro-extraction by packed sorbentsen_US
dc.subjectNon-steroidal anti-inflammatory drugsen_US
dc.subjectPlackett-Burman designsen_US
dc.subjectStatistical experimental designen_US
dc.subjectTraditional methodologiesen_US
dc.subjectUltrahigh pressureen_US
dc.subjectBody fluidsen_US
dc.subjectChromatographyen_US
dc.subjectExtractionen_US
dc.subjectHigh pressure liquid chromatographyen_US
dc.subjectOptimizationen_US
dc.subjectSorbentsen_US
dc.subjectSorptionen_US
dc.subjectDrug productsen_US
dc.subjectacetonitrileen_US
dc.subjectacetylsalicylic aciden_US
dc.subjectdiclofenacen_US
dc.subjectibuprofenen_US
dc.subjectketoprofenen_US
dc.subjectnaproxenen_US
dc.subjectnonsteroid antiinflammatory agenten_US
dc.subjectsorbenten_US
dc.subjecttrifluoroacetic aciden_US
dc.subjectaqueous solutionen_US
dc.subjectarticleen_US
dc.subjectconcentration (parameters)en_US
dc.subjectcontrolled studyen_US
dc.subjectexperimental designen_US
dc.subjectextraction and extractsen_US
dc.subjecthumanen_US
dc.subjectlimit of detectionen_US
dc.subjectlimit of quantitationen_US
dc.subjectlinear systemen_US
dc.subjectmeasurement accuracyen_US
dc.subjectmicroextraction by packed sorbenten_US
dc.subjectmolecular stabilityen_US
dc.subjectPlackett Burman designen_US
dc.subjectpriority journalen_US
dc.subjectprocess optimizationen_US
dc.subjectquantitative analysisen_US
dc.subjectreliabilityen_US
dc.subjectultra performance liquid chromatographyen_US
dc.subjecturinalysisen_US
dc.subjectvalidation studyen_US
dc.subjectAnti-Inflammatory Agents, Non-Steroidalen_US
dc.subjectChromatography, High Pressure Liquiden_US
dc.subjectChromatography, Reverse-Phaseen_US
dc.subjectHumansen_US
dc.subjectLimit of Detectionen_US
dc.subjectSolid Phase Microextractionen_US
dc.titleApplication of statistical experimental design to the optimisation of microextraction by packed sorbent for the analysis of nonsteroidal anti-inflammatory drugs in human urine by ultra-high pressure liquid chromatographyen_US
dc.typeArticleen_US
dc.identifier.volume1304en_US
dc.identifier.startpage1
dc.identifier.startpage1en_US
dc.identifier.endpage9en_US
dc.identifier.doi10.1016/j.chroma.2013.06.047-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid23876769en_US
dc.identifier.scopus2-s2.0-84881025521en_US
dc.identifier.wosWOS:000323017500001en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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