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Method development for acetyl octapeptide-3 analysis by liquid chromatography-tandem mass spectrometry

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dc.contributor.authorJi, Moongi-
dc.contributor.authorLee, Hyeon-Seong-
dc.contributor.authorKim, Youngbae-
dc.contributor.authorSeo, Chan-
dc.contributor.authorChoi, Subin-
dc.contributor.authorOh, Songjin-
dc.contributor.authorMin, Jeuk-
dc.contributor.authorPark, Hyung-Jin-
dc.contributor.authorKim, Jung Dong-
dc.contributor.authorJeong, Do Hyeon-
dc.contributor.authorPaik, Man-Jeong-
dc.date.accessioned2022-09-02T01:10:29Z-
dc.date.available2022-09-02T01:10:29Z-
dc.date.created2022-07-14-
dc.date.issued2020-08-
dc.identifier.issn2093-3134-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/190028-
dc.description.abstractBackground Acetyl octapeptide-3 (SNAP-8) is an antiaging peptide that is more effective than acetyl hexapeptide-3, which is more stable than botulinum toxin and effectively relieves facial wrinkles. Products containing SNAP-8 such as patch are producing, but analytical method has not been reported to determination of SNAP-8. Method Mobile phase, collision energy, and desolvation line temperature were optimized, and mass spectral data set for SNAP-8 was newly constructed by liquid chromatography-triple quadrupole mass spectrometer in multiple reaction monitoring mode. Results The developed method showed good linearity (r >= 0.9971) with limit of quantification of 0.0125 ng/mL, repeatability (% relative standard deviation = 0.02 to 0.12) and accuracy (% relative error = - 1.68 to 1.44) under optimal conditions. This method was successfully applied to a biodegradable microneedle patch loaded with SNAP-8. Conclusion The present method for the quantification of SNAP-8 may be useful for quality control in the cosmetic fields.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringerOpen-
dc.relation.isPartOfJournal of analytical science and technology-
dc.relation.isPartOfJOURNAL OF ANALYTICAL SCIENCE AND TECHNOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleMethod development for acetyl octapeptide-3 analysis by liquid chromatography-tandem mass spectrometry-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentOthers-
dc.contributor.googleauthorJi, Moongi-
dc.contributor.googleauthorLee, Hyeon-Seong-
dc.contributor.googleauthorKim, Youngbae-
dc.contributor.googleauthorSeo, Chan-
dc.contributor.googleauthorChoi, Subin-
dc.contributor.googleauthorOh, Songjin-
dc.contributor.googleauthorMin, Jeuk-
dc.contributor.googleauthorPark, Hyung-Jin-
dc.contributor.googleauthorKim, Jung Dong-
dc.contributor.googleauthorJeong, Do Hyeon-
dc.contributor.googleauthorPaik, Man-Jeong-
dc.identifier.doi10.1186/s40543-020-00232-8-
dc.relation.journalcodeJ03959-
dc.identifier.eissn2093-3371-
dc.subject.keywordAcetyl octapeptide-3-
dc.subject.keywordMicroneedle Patch-
dc.subject.keywordMultiple reaction monitoring mode-
dc.subject.keywordLiquid chromatography-tandem mass spectrometry-
dc.contributor.affiliatedAuthorKim, Jung Dong-
dc.contributor.affiliatedAuthorJeong, Do Hyeon-
dc.identifier.scopusid2-s2.0-85089363073-
dc.identifier.wosid000560102700001-
dc.citation.volume11-
dc.citation.number1-
dc.identifier.bibliographicCitationJournal of analytical science and technology, Vol.11(1), 2020-08-
dc.identifier.rimsid74867-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAcetyl octapeptide-3-
dc.subject.keywordAuthorMicroneedle Patch-
dc.subject.keywordAuthorMultiple reaction monitoring mode-
dc.subject.keywordAuthorLiquid chromatography-tandem mass spectrometry-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusMIMICS-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalResearchAreaChemistry-
dc.identifier.articleno34-
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