In vitro controlled release of vinpocetine-cyclodextrin-tartaric acid multicomponent complexes from HPMC swellable tablets

• Type: Article in International Scientific Journal
• Date: 2005

Authors

Ribeiro, L (Author) Other; Ferreira, DC (Author) FFUP; Veiga, FJB (Author) Other

Journal

Title: Journal of Controlled Release

Vol. 103

Pages: 325-339

ISSN: 0168-3659

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 33 Citations

Scopus - 42 Citations

Scientific classification

FOS: Natural sciences > Chemical sciences

Other information

Authenticus ID: P-000-470

DOI: 10.1016/j.jconrel.2004.12.001

Abstract (EN): The objective of this study was to investigate the effect of multicomponent complexation (MCC) of vinpocetine (VP), a poorly soluble base-type drug, with beta-cyclodextrin (CD), sulfobutylether 0-cyclodextrin (SBE beta CD), tartaric acid (TA), polyvinylpyrrolidone (PVP) and hydroxypropylmethylcellulose (HPMC), on the design of controlled release hydrophilic HPMC tablets and to evaluate their in vitro release profiles by a pH gradient method. Multicomponent complexation led to enhanced dissolution properties of VP both in simulated gastric and intestinal fluids, and became possible the development of HPMC tablet formulations with more independent pH dissolution profiles. Drug release process was investigated experimentally using USP apparatus 3 and by means of model-independent parameters. Responses studied included similarity of dissolution profiles, time for 60% of the drug to dissolve (T-60%), percent of VP released after 7h (PD7h) and the dissolution efficiency parameter at 12 h (DE12 h), Influence of multicomponent complexation was proved to increase the release of VP from HPMC tablets and superior PD7 (h) and DE12 (h) values were obtained in formulations containing VP-CD-TA complexes. Results supported the use of HPMC matrices to provide a useful tool in retarding the release of VP and that dissolution characteristics of the drug may be modulated by multicomponent complexation in these delivery systems, suggesting an improvement on VP bioavailability.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 15