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dc.contributor.authorPhonphok N.
dc.contributor.authorChidichimo G.
dc.contributor.authorWesterman P.W.
dc.date.accessioned2021-04-05T04:33:49Z-
dc.date.available2021-04-05T04:33:49Z-
dc.date.issued1996
dc.identifier.issn93084
dc.identifier.other2-s2.0-0030590459
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15371-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0030590459&doi=10.1016%2f0009-3084%2896%2902590-X&partnerID=40&md5=345e30a69f80deb393b539b2885a7139
dc.description.abstractThe interaction of chloroform with bilayers of dimyristoylphosphatidylcholine (DMPC) has been studied by deuterium and phosphorus-31 nuclear magnetic resonance (NMR). Orientational order has been measured as a function of temperature at many sites in DMPC, water and chloroform for aqueous multilamellar dispersions of the lipid. At equivalent temperatures above the main phase transition temperature for a molar ratio of DMPC to chloroform of approximately 10 to 1, disordering at several sites in the head group of DMPC is observed, unlike the acyl chains where no disordering is observed. With higher concentrations of chloroform (DMPC/chloroform ~ 4:1) greater disordering occurs at the same head group sites and is accompanied by disordering of the acyl chains. The pattern of solvent-induced changes in DMPC is similar to that produced by benzyl alcohol and n-alkanols. With 2H-labelled chloroform, the 2H-NMR spectra show two components, one isotropic and the other ordered(Δv ~ 1.5 kHz) arising from solute intercalated in the bilayer. In DMPC/water systems at low hydration the ordering of the 2H2O in the Lα phase is little affected by chloroform at comparable temperatures whereas at temperatures below the main phase temperature a large disordering of the water is observed. A model of the mode of interaction between chloroform and DMPC is proposed, in which the chloroform is localized principally in an ordered environment in the vicinity of the choline head group at lower temperatures and solute concentrations. Increasing either of these parameters favors the penetration of the chloroform into the center of the bilayer.
dc.subjectalkanol
dc.subjectanesthetic agent
dc.subjectbenzyl alcohol
dc.subjectchloroform
dc.subjectdimyristoylphosphatidylcholine
dc.subjectanesthesia
dc.subjectarticle
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectdrug disposition
dc.subjectisotope labeling
dc.subjectlipid bilayer
dc.subjectnuclear magnetic resonance spectroscopy
dc.subjectphase transition
dc.subjectphospholipid membrane
dc.subjectpriority journal
dc.subjectproton nuclear magnetic resonance
dc.subjecttemperature sensitivity
dc.titleDisposition of chloroform in phosphatidylcholine membranes: A 2H- and 31P-NMR study
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationChemistry and Physics of Lipids. Vol 83, No.1 (1996), p.25-37
dc.identifier.doi10.1016/0009-3084(96)02590-X
Appears in Collections:Scopus 1983-2021

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