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...
- 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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| 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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http://purl.org/coar/resource_type/c_2df8fbb1 |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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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]. |
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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 |
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https://hdl.handle.net/10495/34484 |
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eng |
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eng |
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Biochim. Biophys. Acta. Biomembr. |
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1303 |
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6 |
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1296 |
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1788 |
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Biochimica et Biophysica Acta - Biomembranes |
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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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