Multicomponent complex formation between vinpocetine, cyclodextrins, tartaric acid and water-soluble polymers monitored by NMR and solubility studies

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

Autores

Ribeiro, L (Autor) Outra; Carvalho, RA (Autor) Outra; Ferreira, DC (Autor) FFUP; Veiga, FJB (Autor) Outra

Revista

Título: European Journal of Pharmaceutical Sciences

Vol. 24

Páginas: 1-13

ISSN: 0928-0987

Editora: Elsevier

Indexação

ISI Web of Knowledge - 60 Citações

Scopus - 80 Citações

Classificação Científica

FOS: Ciências médicas e da saúde > Medicina básica

Outras Informações

ID Authenticus: P-000-5PH

DOI: 10.1016/j.ejps.2004.09.003

Abstract (EN): This work deals with multicomponent complex formation of vinpocetine (VP) with beta-cyclodextrin (betaCD), sulfobutyl ether beta-cyclodextrin (SBEbetaCD) and tartaric acid (TA), in the presence or absence of water-soluble polymers, in aqueous solution. Complexation was monitored by phase-solubility and proton nuclear magnetic resonance (H-1 NMR) studies. TA demonstrated a synergistic effect on VP solubility, and in the complexation efficiency of betaCD and SBEbetaCD. Additionally, water-soluble polymers increased even more the complexation efficiency of the CDs that was reflected by a 2.1-2.5 increase on K-C values for VP-CD-TA-polymer multicomponent complexes. SBEbetaCD was more effective in VP solubilization, as K-C values of VP-SBEbetaCD-TA multicomponent complexes were notably higher than in corresponding betaCD complexes. The large chemical shift displacements from protons located in the interior of the hydrophobic CD cavities (i.e., H-3 and H-5) coupled with significant chemical shift displacements of VP aromatic protons suggested that this moiety was included in the cavity of both betaCD and SBEbetaCD. Two-dimensional rotating frame nuclear Overhauser effect spectroscopy (ROESY) experiments were carried out in order to obtain information about the multicomponent complex geometry in solution. Inspection of ROESY spectra allowed the establishment of spatial proximities between all aromatic protons of VP and the internal protons of the CDs, confirming that the aromatic moiety of VP is included in CD cavities being deeply inserted in SBEbetaCD multicomponent complexes, since additional interactions with the suffobutyl side chains were evidenced. (C) 2004 Elsevier B.V. All right, reserved.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 13