nanodispersions

7413's picture

Dissolution Rate and Stability Study of Flavanone Aglycones, ‎Naringenin And Hesperetin, By Drug Delivery Systems Based on ‎Polyvinylpyrrolidone (PVP) Nanodispersions

Journal Title, Volume, Page: 
Drug Development and Industrial Pharmacy, Volume 36, Number 3
Year of Publication: 
2010
Authors: 
Kanaze, F.I.
Department of Pharmaceutics and Drug Control, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece
Current Affiliation: 
Department of Pharmacy,Faculty of Medicine & Health Sciences, An-Najah National University, Nablus, Palestine
Kokkalou, E.
Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece
Niopas, I.
Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece
Barmpalexis, P.
Department of Pharmaceutics and Drug Control, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece
Georgarakis, E.
Department of Pharmaceutics and Drug Control, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece
Bikiaris, D.
Laboratory of Organic Chemical Technology, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece
Preferred Abstract (Original): 

Objective: To study the dissolution behavior, the release mechanism and the stability of nanodispersion system of aglycones with PVP. Methods: The nanodispersion system of polyvinylpyrrolidone (PVP)/naringenin–hesperetin was prepared using the solvent evaporation method. The chemical stability (compatibility) of naringenin and hesperetin in the prepared dispersions was studied under accelerated conditions for 3 months. The evaluation of physical stability was performed by X-ray diffraction analysis (XRD) and by comparing the dissolution profile before and after storage at high temperature and moisture (40ºC, RH 75%). Results: The dissolution rate of naringenin and hesperetin released was dramatically increased in the nanodispersion system of PVP/naringenin–hesperetin (80/20, w/w). The release mechanism of both flavanone aglycones was better described by the diffusion model (Higuchi model). Also it was found that the rate-limiting step that controlled the release of naringenin and hesperetin in the nanodispersion system was dissolution of the carrier (PVP). Conclusions: During accelerated degradation analysis, for 3 months at high temperature and moisture, PVP nanodispersion system showed enhanced chemical compatibility and physical stability. The physical evaluation (obtained from XRD analysis) of PVP/naringenin–hesperetin (80/20, w/w) in the selected storage conditions did not show any crystallization of flavanone aglycones in the PVP nanodispersion system or any change in their release profile.

Syndicate content