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Determination of Sufentanil in Human Plasma Using Ultra-high Performance Liquid Chromatography Coupled with Tandem Mass Spectrometry (UPLC-MS/MS)

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dc.contributor.authorLee, Sang-Min-
dc.contributor.authorKim, Suin-
dc.contributor.authorShin, Dongseong-
dc.contributor.authorShin, Kwang-Hee-
dc.date.accessioned2023-12-28T01:30:19Z-
dc.date.available2023-12-28T01:30:19Z-
dc.date.issued2023-09-
dc.identifier.issn1573-4110-
dc.identifier.issn1875-6727-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/89836-
dc.description.abstractBackground Sufentanil, an opioid analgesic, is used as an induction agent for general anesthesia during surgery. Sufentanil is more active than other anesthetics and has a narrow therapeutic range. Therefore, a precise dosage regimen is necessary when administering sufentanil.Objective This study aimed to develop a bioanalytical method for the determination of sufentanil within the sensitive concentration range more than that in a previous study utilizing protein precipitation (PP) and determine the plasma concentration of sufentanil.Methods A method for quantitating sufentanil was developed using ultra-high performance liquid chromatography coupled with mass spectrometry (UPLC-MS/MS) and detection by electrospray ionization (ESI). The internal standard was sufentanil-d5. Chromatographic separation was performed using an Acquity UPLC HSS T3 column (50 x 2.1 mm, 1.8 mu m) from Waters (Milford, MA, USA). Protein precipitation (PP) was used for sample preparation, and gradient elution was conducted using a mobile phase consisting of 1 mL of 2M ammonium acetate in 99% formic acid in 1 L of water or in 1 L of acetonitrile. The total run time for the analysis was 5 min, and the flow rate was 0.4 mL/min.Results Standard curves were linear over ranges of 0.025-30 ng/mL for sufentanil with a correlation coefficient (r2) greater than 0.9998. The lower limit of quantification (LLOQ) was 0.025 ng/mL. The intra- and inter-day accuracies were 97.66%-108.8% and 101.25%-103.17%, respectively, and the precision did not exceed 15% for sufentanil.Conclusion This study developed a validated, simple, sensitive, and convenient UPLC-MS/MS method for quantifying sufentanil in human plasma. This method was applied to determine sufentanil concentration in the plasma of patients undergoing surgery. The bioanalytical method using PP showed a sufficiently sensitive concentration range. This method could be applied to various pharmacokinetic studies of sufentanil.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherBENTHAM SCIENCE PUBL LTD-
dc.titleDetermination of Sufentanil in Human Plasma Using Ultra-high Performance Liquid Chromatography Coupled with Tandem Mass Spectrometry (UPLC-MS/MS)-
dc.typeArticle-
dc.identifier.wosid001117125900005-
dc.identifier.doi10.2174/1573411019666230823094749-
dc.identifier.bibliographicCitationCURRENT ANALYTICAL CHEMISTRY, v.19, no.7, pp 531 - 540-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85180221603-
dc.citation.endPage540-
dc.citation.startPage531-
dc.citation.titleCURRENT ANALYTICAL CHEMISTRY-
dc.citation.volume19-
dc.citation.number7-
dc.type.docTypeArticle-
dc.publisher.location아랍에미리트-
dc.subject.keywordAuthorSufentanil-
dc.subject.keywordAuthorhuman plasma-
dc.subject.keywordAuthorbioanalysis-
dc.subject.keywordAuthorUPLC-MS/MS-
dc.subject.keywordAuthorprotein precipitation (PP)-
dc.subject.keywordAuthorMRM-
dc.subject.keywordPlusHUMAN SERUM-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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