The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids

ABSTRACT: Nonsteroidal anti-inflammatory drugs (NSAIDs) represent non-specific inhibitors of the cycloxygenase pathway of inflammation, and therefore an understanding of the interaction process of the drugs with membrane phospholipids is of high relevance. We have studied the interaction of the NSAI...

Full description

Autores:
Manrique Moreno, Marcela María
Garidel, Patrick
Suwalsky, Mario
Howe, Jörg
Brandenburg, Klaus
Tipo de recurso:
Article of investigation
Fecha de publicación:
2009
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/34484
Acceso en línea:
https://hdl.handle.net/10495/34484
Palabra clave:
Antiinflamatorios no Esteroideos
Anti-Inflammatory Agents, Non-Steroidal
Inhibidores de la Ciclooxigenasa
Cyclooxygenase Inhibitors
Glicosilfosfatidilinositoles
Glycosylphosphatidylinositols
Rastreo Diferencial de Calorimetría
Calorimetry, Differential Scanning
Diclofenaco
Diclofenac
Dimiristoilfosfatidilcolina
Dimyristoylphosphatidylcholine
Transferencia Resonante de Energía de Fluorescencia
Fluorescence Resonance Energy Transfer
Ibuprofeno
Ibuprofen
Lecitinas
Lecithins
Liposomas
Liposomes
Naproxeno
Naproxen
Espectrofotometría Infrarroja
Spectrophotometry, Infrared
Espectroscopía Infrarroja por Transformada de Fourier
Spectroscopy, Fourier Transform Infrared
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
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network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
title The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
spellingShingle The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
Antiinflamatorios no Esteroideos
Anti-Inflammatory Agents, Non-Steroidal
Inhibidores de la Ciclooxigenasa
Cyclooxygenase Inhibitors
Glicosilfosfatidilinositoles
Glycosylphosphatidylinositols
Rastreo Diferencial de Calorimetría
Calorimetry, Differential Scanning
Diclofenaco
Diclofenac
Dimiristoilfosfatidilcolina
Dimyristoylphosphatidylcholine
Transferencia Resonante de Energía de Fluorescencia
Fluorescence Resonance Energy Transfer
Ibuprofeno
Ibuprofen
Lecitinas
Lecithins
Liposomas
Liposomes
Naproxeno
Naproxen
Espectrofotometría Infrarroja
Spectrophotometry, Infrared
Espectroscopía Infrarroja por Transformada de Fourier
Spectroscopy, Fourier Transform Infrared
title_short The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
title_full The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
title_fullStr The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
title_full_unstemmed The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
title_sort The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipids
dc.creator.fl_str_mv Manrique Moreno, Marcela María
Garidel, Patrick
Suwalsky, Mario
Howe, Jörg
Brandenburg, Klaus
dc.contributor.author.none.fl_str_mv Manrique Moreno, Marcela María
Garidel, Patrick
Suwalsky, Mario
Howe, Jörg
Brandenburg, Klaus
dc.contributor.researchgroup.spa.fl_str_mv Grupo Interdisciplinario de Estudios Moleculares
dc.subject.decs.none.fl_str_mv Antiinflamatorios no Esteroideos
Anti-Inflammatory Agents, Non-Steroidal
Inhibidores de la Ciclooxigenasa
Cyclooxygenase Inhibitors
Glicosilfosfatidilinositoles
Glycosylphosphatidylinositols
Rastreo Diferencial de Calorimetría
Calorimetry, Differential Scanning
Diclofenaco
Diclofenac
Dimiristoilfosfatidilcolina
Dimyristoylphosphatidylcholine
Transferencia Resonante de Energía de Fluorescencia
Fluorescence Resonance Energy Transfer
Ibuprofeno
Ibuprofen
Lecitinas
Lecithins
Liposomas
Liposomes
Naproxeno
Naproxen
Espectrofotometría Infrarroja
Spectrophotometry, Infrared
Espectroscopía Infrarroja por Transformada de Fourier
Spectroscopy, Fourier Transform Infrared
topic Antiinflamatorios no Esteroideos
Anti-Inflammatory Agents, Non-Steroidal
Inhibidores de la Ciclooxigenasa
Cyclooxygenase Inhibitors
Glicosilfosfatidilinositoles
Glycosylphosphatidylinositols
Rastreo Diferencial de Calorimetría
Calorimetry, Differential Scanning
Diclofenaco
Diclofenac
Dimiristoilfosfatidilcolina
Dimyristoylphosphatidylcholine
Transferencia Resonante de Energía de Fluorescencia
Fluorescence Resonance Energy Transfer
Ibuprofeno
Ibuprofen
Lecitinas
Lecithins
Liposomas
Liposomes
Naproxeno
Naproxen
Espectrofotometría Infrarroja
Spectrophotometry, Infrared
Espectroscopía Infrarroja por Transformada de Fourier
Spectroscopy, Fourier Transform Infrared
description ABSTRACT: Nonsteroidal anti-inflammatory drugs (NSAIDs) represent non-specific inhibitors of the cycloxygenase pathway of inflammation, and therefore an understanding of the interaction process of the drugs with membrane phospholipids is of high relevance. We have studied the interaction of the NSAIDs with phospholipid membranes made from dimyristoylphosphatidylcholine (DMPC) by applying Fourier-transform infrared spectroscopy (FTIR), Förster resonance energy transfer spectroscopy (FRET), differential scanning calorimetry (DSC) and isothermal titration calorimetry (ITC). FTIR data obtained via attenuated total reflectance (ATR) show that the interaction between DMPC and NSAIDs is limited to a strong interaction of the drugs with the phosphate region of the lipid head group. The FTIR transmission data furthermore are indicative of a strong effect of the drugs on the hydrocarbon chains inducing a reduction of the chain–chain interactions, i.e., a fluidization effect. Parallel to this, from the DSC data beside the decrease of Tm a reduction of the peak height of the melting endotherm connected with its broadening is observed, but leaving the overall phase transition enthalpy constant. Additionally, phase separation is observed, inducing the formation of a NSAID-rich and a NSAID-poor phase. This is especially pronounced for Diclofenac. Despite the strong influence of the drugs on the acyl chain moiety, FRET data do not reveal any evidence for drug incorporation into the lipid matrix, and ITC measurements performed do not exhibit any heat production due to drug binding.
publishDate 2009
dc.date.issued.none.fl_str_mv 2009
dc.date.accessioned.none.fl_str_mv 2023-04-06T23:20:04Z
dc.date.available.none.fl_str_mv 2023-04-06T23:20:04Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Manrique-Moreno M, Garidel P, Suwalsky M, Howe J, Brandenburg K. The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: a physico-chemical study with lecithin phospholipids. Biochim Biophys Acta. 2009 Jun;1788(6):1296-303. doi: 10.1016/j.bbamem.2009.01.016. Epub 2009 Feb 6. Erratum in: Biochim Biophys Acta. 2011 Jul;1808(7):1946. Moreno, Marcela Manrique [corrected to Manrique-Moreno, Marcela].
dc.identifier.issn.none.fl_str_mv 0005-2736
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/34484
dc.identifier.doi.none.fl_str_mv 10.1016/j.bbamem.2009.01.016
dc.identifier.eissn.none.fl_str_mv 1879-2642
identifier_str_mv Manrique-Moreno M, Garidel P, Suwalsky M, Howe J, Brandenburg K. The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: a physico-chemical study with lecithin phospholipids. Biochim Biophys Acta. 2009 Jun;1788(6):1296-303. doi: 10.1016/j.bbamem.2009.01.016. Epub 2009 Feb 6. Erratum in: Biochim Biophys Acta. 2011 Jul;1808(7):1946. Moreno, Marcela Manrique [corrected to Manrique-Moreno, Marcela].
0005-2736
10.1016/j.bbamem.2009.01.016
1879-2642
url https://hdl.handle.net/10495/34484
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Biochim. Biophys. Acta. Biomembr.
dc.relation.citationendpage.spa.fl_str_mv 1303
dc.relation.citationissue.spa.fl_str_mv 6
dc.relation.citationstartpage.spa.fl_str_mv 1296
dc.relation.citationvolume.spa.fl_str_mv 1788
dc.relation.ispartofjournal.spa.fl_str_mv Biochimica et Biophysica Acta - Biomembranes
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dc.publisher.place.spa.fl_str_mv Ámsterdam, Países Bajos
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spelling Manrique Moreno, Marcela MaríaGaridel, PatrickSuwalsky, MarioHowe, JörgBrandenburg, KlausGrupo Interdisciplinario de Estudios Moleculares2023-04-06T23:20:04Z2023-04-06T23:20:04Z2009Manrique-Moreno M, Garidel P, Suwalsky M, Howe J, Brandenburg K. The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: a physico-chemical study with lecithin phospholipids. Biochim Biophys Acta. 2009 Jun;1788(6):1296-303. doi: 10.1016/j.bbamem.2009.01.016. Epub 2009 Feb 6. Erratum in: Biochim Biophys Acta. 2011 Jul;1808(7):1946. Moreno, Marcela Manrique [corrected to Manrique-Moreno, Marcela].0005-2736https://hdl.handle.net/10495/3448410.1016/j.bbamem.2009.01.0161879-2642ABSTRACT: Nonsteroidal anti-inflammatory drugs (NSAIDs) represent non-specific inhibitors of the cycloxygenase pathway of inflammation, and therefore an understanding of the interaction process of the drugs with membrane phospholipids is of high relevance. We have studied the interaction of the NSAIDs with phospholipid membranes made from dimyristoylphosphatidylcholine (DMPC) by applying Fourier-transform infrared spectroscopy (FTIR), Förster resonance energy transfer spectroscopy (FRET), differential scanning calorimetry (DSC) and isothermal titration calorimetry (ITC). FTIR data obtained via attenuated total reflectance (ATR) show that the interaction between DMPC and NSAIDs is limited to a strong interaction of the drugs with the phosphate region of the lipid head group. The FTIR transmission data furthermore are indicative of a strong effect of the drugs on the hydrocarbon chains inducing a reduction of the chain–chain interactions, i.e., a fluidization effect. Parallel to this, from the DSC data beside the decrease of Tm a reduction of the peak height of the melting endotherm connected with its broadening is observed, but leaving the overall phase transition enthalpy constant. Additionally, phase separation is observed, inducing the formation of a NSAID-rich and a NSAID-poor phase. This is especially pronounced for Diclofenac. Despite the strong influence of the drugs on the acyl chain moiety, FRET data do not reveal any evidence for drug incorporation into the lipid matrix, and ITC measurements performed do not exhibit any heat production due to drug binding.COL000746210application/pdfengElsevierÁmsterdam, Países Bajoshttps://creativecommons.org/licenses/by-nc-nd/4.0/http://creativecommons.org/licenses/by-nc-nd/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2The membrane-activity of Ibuprofen, Diclofenac, and Naproxen: A physico-chemical study with lecithin phospholipidsArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAntiinflamatorios no EsteroideosAnti-Inflammatory Agents, Non-SteroidalInhibidores de la CiclooxigenasaCyclooxygenase InhibitorsGlicosilfosfatidilinositolesGlycosylphosphatidylinositolsRastreo Diferencial de CalorimetríaCalorimetry, Differential ScanningDiclofenacoDiclofenacDimiristoilfosfatidilcolinaDimyristoylphosphatidylcholineTransferencia Resonante de Energía de FluorescenciaFluorescence Resonance Energy TransferIbuprofenoIbuprofenLecitinasLecithinsLiposomasLiposomesNaproxenoNaproxenEspectrofotometría InfrarrojaSpectrophotometry, InfraredEspectroscopía Infrarroja por Transformada de FourierSpectroscopy, Fourier Transform InfraredBiochim. Biophys. Acta. 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