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231223s2010 xx |||||o 00| ||eng c |
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|a 10.1021/la1022714
|2 doi
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|a pubmed24n0673.xml
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|a (NLM)20883049
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Thompson, Katherine C
|e verfasserin
|4 aut
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|a Reaction of a phospholipid monolayer with gas-phase ozone at the air-water interface
|b measurement of surface excess and surface pressure in real time
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|c 2010
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 04.03.2011
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|a Date Revised 21.11.2013
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a The reaction between gas-phase ozone and monolayers of the unsaturated lipid 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine, POPC, on aqueous solutions has been studied in real time using neutron reflection and surface pressure measurements. The reaction between ozone and lung surfactant, which contains POPC, leads to decreased pulmonary function, but little is known about the changes that occur to the interfacial material as a result of oxidation. The results reveal that the initial reaction of ozone with POPC leads to a rapid increase in surface pressure followed by a slow decrease to very low values. The neutron reflection measurements, performed on an isotopologue of POPC with a selectively deuterated palmitoyl strand, reveal that the reaction leads to loss of this strand from the air-water interface, suggesting either solubilization of the product lipid or degradation of the palmitoyl strand by a reactive species. Reactions of (1)H-POPC on D(2)O reveal that the headgroup region of the lipids in aqueous solution is not dramatically perturbed by the reaction of POPC monolayers with ozone supporting degradation of the palmitoyl strand rather than solubilization. The results are consistent with the reaction of ozone with the oleoyl strand of POPC at the air-water interface leading to the formation of OH radicals. The highly reactive OH radicals produced can then go on to react with the saturated palmitoyl strands leading to the formation of oxidized lipids with shorter alkyl tails
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a 1-palmitoyl-2-(9-oxononanoyl)-sn-glycero-3-phosphocholine
|2 NLM
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|a Phosphatidylcholines
|2 NLM
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|a Water
|2 NLM
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|a 059QF0KO0R
|2 NLM
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|a 1,2-Dipalmitoylphosphatidylcholine
|2 NLM
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|a 2644-64-6
|2 NLM
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|a Ozone
|2 NLM
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|a 66H7ZZK23N
|2 NLM
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|a Oxygen
|2 NLM
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|a S88TT14065
|2 NLM
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|a 1-palmitoyl-2-oleoylphosphatidylcholine
|2 NLM
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|a TE895536Y5
|2 NLM
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|a Rennie, Adrian R
|e verfasserin
|4 aut
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|a King, Martin D
|e verfasserin
|4 aut
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|a Hardman, Samantha J O
|e verfasserin
|4 aut
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|a Lucas, Claire O M
|e verfasserin
|4 aut
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|a Pfrang, Christian
|e verfasserin
|4 aut
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|a Hughes, Brian R
|e verfasserin
|4 aut
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|a Hughes, Arwel V
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 26(2010), 22 vom: 16. Nov., Seite 17295-303
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:26
|g year:2010
|g number:22
|g day:16
|g month:11
|g pages:17295-303
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|u http://dx.doi.org/10.1021/la1022714
|3 Volltext
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