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/
Description
Summary: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.