Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/28727
DC FieldValueLanguage
dc.contributor.advisorTapia, M. J.-
dc.contributor.authorTapia, M. J.-
dc.contributor.authorMonteserín, M.-
dc.contributor.authorBurrows, H. D.-
dc.contributor.authorAlmeida, J. A. S.-
dc.contributor.authorPais, A. A. C. C.-
dc.contributor.authorPina, J.-
dc.contributor.authorSeixas de Melo, J. S.-
dc.contributor.authorJarmelo, S.-
dc.contributor.authorEstelrich, J.-
dc.date.accessioned2015-05-13T16:06:00Z-
dc.date.available2015-05-13T16:06:00Z-
dc.date.issued2014-11-05-
dc.identifier.issn1744-6848-
dc.identifier.urihttp://hdl.handle.net/10316/28727-
dc.description.abstractThe combination of various experimental techniques with theoretical simulations has allowed elucidation of the mode of incorporation of fluorene based derivatives into phospholipid bilayers. Molecular dynamics (MD) simulations on a fully hydrated 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine (DMPC) bilayer, with benzene (B), biphenyl (BP), fluorene (F) and tri-(9,9-di-n-octylfluorenyl-2,7-diyl), TF, have provided insights into the topography of these molecules when they are present in the phospholipid bilayer, and suggest marked differences between the behavior of the small molecules and the oligomer. Further information on the interaction of neutral fluorenes within the phospholipid bilayer was obtained by an infrared (IR) spectroscopic study of films of DMPC and of the phospholipid with PFO deuterated specifically on its alkyl chains (DMPC–PFO-d34). This was complemented by measurements of the effect of F, TF and two neutral polymers: polyfluorene poly(9,9-di-n-octylfluorenyl-2,7-diyl), PFO, and poly(9,9-di-n-dodecylfluorenyl-2,7-diyl), PFD, on the phospholipid phase transition temperature using differential scanning calorimetry (DSC). Changes in liposome size upon addition of F and PFO were followed by dynamic light scattering. In addition, the spectroscopic properties of F, TF, PFO and PFD solubilised in DMPC liposomes (absorption, steady-state and time-resolved fluorescence) were compared with those of the same probes in typical organic solvents (chloroform, cyclohexane and ethanol). Combining the insight from MD simulations with the results at the molecular level from the various experimental techniques suggests that while the small molecules have a tendency to be located in the phospholipid head group region, the polymers are incorporated within the lipid bilayers, with the backbone predominantly orthogonal to the phospholipid alkyl chains and with interdigitation of them and the PFO alkyl chains.por
dc.language.isoengpor
dc.publisherRoyal Society of Chemistrypor
dc.rightsopenAccesspor
dc.titleFrom molecular modelling to photophysics of neutral oligo- and polyfluorenes incorporated into phospholipid bilayerspor
dc.typearticlepor
degois.publication.firstPage303por
degois.publication.lastPage317por
degois.publication.locationRoyal Society of Chemistry, Thomas Graham House, Science Park, Milton Road, Cambridge CB4 0WFpor
degois.publication.titleFrom molecular modelling to photophysics of neutral oligo- and polyfluorenes incorporated into phospholipid bilayers†por
dc.relation.publisherversionpublisher's version/PDFpor
dc.peerreviewedYespor
degois.publication.volume11por
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
Files in This Item:
File Description SizeFormat
Soft Matter2015_11_303.pdf887.67 kBAdobe PDFView/Open
Show simple item record

Page view(s)

219
checked on Dec 10, 2019

Download(s)

125
checked on Dec 10, 2019

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.