Effects of diclofenac on EPC liposome membrane properties

• Tipo: Artigo em Revista Científica Internacional
• Data: 2005

Autores

Ferreira, H (Autor) Outra; Lucio, M (Autor) Outra; Lima, JLFC (Autor) FFUP; Matos, C (Autor) Outra; Reis, S (Autor) FFUP

Revista

Título: Analytical and Bioanalytical Chemistry

Vol. 382

Páginas: 1256-1264

ISSN: 1618-2642

Editora: Springer Nature

Indexação

ISI Web of Knowledge - 38 Citações

ISI Web of Science

Scopus - 38 Citações

Classificação Científica

FOS: Ciências exactas e naturais > Química

CORDIS: Ciências da Saúde

Outras Informações

ID Authenticus: P-000-2DR

DOI: 10.1007/s00216-005-3251-z

Resumo (PT): In this work the interaction of a non-steroidal anti-inflammatory drug (NSAID), diclofenac, with egg yolk phosphatidylcoline (EPC) liposomes, used as cell-membrane models, was quantified by determination of the partition coefficient. The liposome/aqueous phase partition coefficient was determined by derivative spectrophotometry, fluorescence quenching, and measurement of zeta-potential. Theoretical models based on simple partition of the diclofenac between two different media, were used to fit the experimental data, enabling the determination of Kp. The three techniques used yielded similar results. The effects of the interaction on the membranes characteristics were further evaluated, either by studying membrane potential changes or by effects on membrane fluidity. The liposome membrane potential and the size and size-homogeneity of liposomes were measured by light scattering. The effects of diclofenac on the internal viscosity or fluidity of the membrane were determined by use of spectroscopic probes—a series of n-(9-anthroyloxy) fatty acids in which the carboxyl terminal group is located at the interfacial region of the membrane and the fluorescent anthracene group is attached at different positions along the fatty acid chain. The location of the diclofenac on the membrane was also evaluated, by fluorescence quenching using the same series of fluorescent probes. Because the fluorescent anthracene group is attached at different positions along the fatty acid chain, it is possible to label at a graded series of depths in the bilayer. The interactions between the drug and the probe are a means of predicting the location of the drug on the membrane. <br> <br> Keywords Diclofenac - Liposomes - Derivative spectrophotometry - Fluorescence quenching - Anisotropy - Zeta-potential <br> <a target="_blank" href="http://www.springerlink.com/content/n017350274g11568/?p=0b05d8afb1584bddb414161ae7021b5d&pi=9 "> Texto integral </a> <br> <br>

Abstract (EN): In this work the interaction of a non-steroidal anti-inflammatory drug (NSAID), diclofenac, with egg yolk phosphatidylcoline (EPC) liposomes, used as cell-membrane models, was quantified by determination of the partition coefficient. The liposome/aqueous phase partition coefficient was determined by derivative spectrophotometry, fluorescence quenching, and measurement of zeta-potential. Theoretical models based on simple partition of the diclofenac between two different media, were used to fit the experimental data, enabling the determination of K-p. The three techniques used yielded similar results. The effects of the interaction on the membrane's characteristics were further evaluated, either by studying membrane potential changes or by effects on membrane fluidity. The liposome membrane potential and the size and size-homogeneity of liposomes were measured by light scattering. The effects of diclofenac on the internal viscosity or fluidity of the membrane were determined by use of spectroscopic probes-a series of n-(9-anthroyloxy) fatty acids in which the carboxyl terminal group is located at the interfacial region of the membrane and the fluorescent anthracene group is attached at different positions along the fatty acid chain. The location of the diclofenac on the membrane was also evaluated, by fluorescence quenching using the same series of fluorescent probes. Because the fluorescent anthracene group is attached at different positions along the fatty acid chain, it is possible to label at a graded series of depths in the bilayer. The interactions between the drug and the probe are a means of predicting the location of the drug on the membrane.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 9