Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/89943
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorChinese Mainland Affairs Office-
dc.creatorHu, Ben_US
dc.creatorZheng, Ben_US
dc.creatorRickert, Den_US
dc.creatorGómez-Ríos, GAen_US
dc.creatorBojko, Ben_US
dc.creatorPawliszyn, Jen_US
dc.creatorYao, ZPen_US
dc.date.accessioned2021-05-13T08:32:54Z-
dc.date.available2021-05-13T08:32:54Z-
dc.identifier.issn0003-2670en_US
dc.identifier.urihttp://hdl.handle.net/10397/89943-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2019 Elsevier B.V. All rights reserved.en_US
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.en_US
dc.subjectDirect couplingen_US
dc.subjectElectrospray ionization mass spectrometryen_US
dc.subjectKetamineen_US
dc.subjectSolid phase microextractionen_US
dc.subjectUrineen_US
dc.titleDirect coupling of solid phase microextraction with electrospray ionization mass spectrometry : a case study for detection of ketamine in urineen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage112en_US
dc.identifier.epage119en_US
dc.identifier.volume1075en_US
dc.identifier.doi10.1016/j.aca.2019.05.044en_US
dcterms.abstractElectrospray ionization mass spectrometry (ESI-MS) is a commonly used technique for analysis of various samples. Solid phase microextraction (SPME) is a simple and efficient technique that combines both sampling and sample preparation into one consolidated step, preconcentrating extracted analytes for ultra-sensitive analysis. Historically, SPME has been coupled with chromatography-based techniques for sample separation prior to analysis, however more recently, the chromatographic step has been omitted, with the SPME device directly coupled with the mass spectrometer. In this study, direct coupling of SPME with ESI-MS was developed, and extensively validated to quantitate ketamine from human urine, employing a practical experimental workflow and no extensive hardware modification to the equipment. Among the different fibers evaluated, SPME device coated with C18/benzenesulfonic acid particles was selected for the analysis due to its good selectivity and signal response. Different approaches, including desorption spray, dripping, desorption ESI and nano-ESI were attempted for elution and ionization of the analytes extracted using the SPME fibers. The results showed that the desorption spray and nano-ESI methods offered better signal response and signal duration than the others that were evaluated. The analytical performance of the SPME-nano-ESI-MS setup was excellent, including limit of detection (LOD) of 0.027 ng/mL, limit of quantitation (LOQ) of 0.1 ng/mL, linear range of 0.1–500.0 ng/mL (R2 = 0.9995) and recoveries of 90.8–109.4% with RSD 3.4–10.6% for three validation points at 4.0, 40.0 and 400.0 ng/mL, far better than the performance of conventional methods. The results herein presented, demonstrated that the direct coupling of SPME fibers with ESI-MS-based systems allowed for the simple and ultra-sensitive determination of analytes from raw samples such as human urine.-
dcterms.accessRightsopen access-
dcterms.bibliographicCitationAnalytica chimica acta, 10 Oct. 2019, v. 1075, p. 112-119en_US
dcterms.isPartOfAnalytica chimica actaen_US
dcterms.issued2019-10-10-
dc.identifier.scopus2-s2.0-85066235449-
dc.identifier.pmid31196416-
dc.description.validate202105 bcvc-
dc.description.oaAccepted Manuscript-
dc.identifier.FolderNumbera0776-n04-
dc.identifier.SubFormID1542-
dc.description.fundingSourceRGC-
dc.description.fundingTextC5031-14E-
dc.description.pubStatusPublished-
dc.description.oaCategoryGreen (AAM)en_US
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