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dc.contributor.authorChoi, Wanjae-
dc.contributor.authorRyu, Hyunil-
dc.contributor.authorFuwad, Ahmed-
dc.contributor.authorGoh, Seulmini-
dc.contributor.authorZhou, Chaoge-
dc.contributor.authorShim, Jiwook-
dc.contributor.authorTakagi, Masahiro-
dc.contributor.authorKwon, Soonjo-
dc.contributor.authorKim, Sun Min-
dc.contributor.authorJeon, Tae-Joon-
dc.date.accessioned2024-01-19T14:02:35Z-
dc.date.available2024-01-19T14:02:35Z-
dc.date.created2022-04-05-
dc.date.issued2021-08-
dc.identifier.issn2077-0375-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/116606-
dc.description.abstractLocal anesthesia is a drug that penetrates the nerve cell membrane and binds to the voltage gate sodium channel, inhibiting the membrane potential and neurotransmission. It is mainly used in clinical uses to address the pain of surgical procedures in the local area. Local anesthetics (LAs), however, can be incorporated into the membrane, reducing the thermal stability of the membrane as well as altering membrane properties such as fluidity, permeability, and lipid packing order. The effects of LAs on the membrane are not yet fully understood, despite a number of previous studies. In particular, it is necessary to analyze which is the more dominant factor, the membrane affinity or the structural perturbation of the membrane. To analyze the effects of LAs on the cell membrane and compare the results with those from model membranes, morphological analysis and 50% inhibitory concentration (IC50) measurement of CCD-1064sk (fibroblast, human skin) membranes were carried out for lidocaine (LDC) and tetracaine (TTC), the most popular LAs in clinical use. Furthermore, the membrane affinity of the LAs was quantitatively analyzed using a colorimetric polydiacetylene assay, where the color shift represents their distribution in the membrane. Further, to confirm the membrane affinity and structural effects of the membranes, we performed an electrophysiological study using a model protein (gramicidin A, gA) and measured the channel lifetime of the model protein on the free-standing lipid bilayer according to the concentration of each LA. Our results show that when LAs interact with cell membranes, membrane affinity is a more dominant factor than steric or conformational effects of the membrane.-
dc.languageEnglish-
dc.publisherMDPI-
dc.titleQuantitative Analysis of the Membrane Affinity of Local Anesthetics Using a Model Cell Membrane-
dc.typeArticle-
dc.identifier.doi10.3390/membranes11080579-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMembranes, v.11, no.8-
dc.citation.titleMembranes-
dc.citation.volume11-
dc.citation.number8-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000689587600001-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPolymer Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusPOLYDIACETYLENE VESICLES-
dc.subject.keywordPlusCHANNEL FUNCTION-
dc.subject.keywordPlusLIPID-BILAYERS-
dc.subject.keywordPlusGRAMICIDIN-
dc.subject.keywordPlusLIDOCAINE-
dc.subject.keywordPlusSODIUM-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusBLOCK-
dc.subject.keywordAuthorlocal anesthetics-
dc.subject.keywordAuthormembrane affinity-
dc.subject.keywordAuthorlipid bilayer membrane-
dc.subject.keywordAuthorcalorimetric assay-
dc.subject.keywordAuthorcramicidin A-
dc.subject.keywordAuthorfibroblast cells-
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KIST Article > 2021
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