Characterization and physical stability of spray dried solid dispersions of probucol and PVP-K30

Pia Thybo, Betty L Pedersen, Lars Hovgaard, Rene Holm, Anette Mullertz

    Research output: Contribution to journalJournal articleResearchpeer-review

    64 Citations (Scopus)

    Abstract

    The main purpose of this study was to obtain stable, well-characterized solid dispersions (SDs) of amorphous probucol and polyvinylpyrrolidone K-30 (PVP-K30) with improved dissolution rates. A secondary aim was to investigate the flow-through dissolution method for in-vitro dissolution measurements of small-sized amorphous powders dispersed in a hydrophilic polymer. SDs were prepared by spray drying solutions of probucol and different amounts of PVP-K30. The obtained SDs were characterized by dissolution rate measurements in a flow-through apparatus, X-ray Powder Diffraction (XRPD), Differential Scanning Calorimetry (DSC), Scanning Electron Microscopy (SEM), particle sizing (laser diffraction) and Brunauer-Emmett-Teller Method (BET) and results were compared with starting material and a physical mixture. The physical stability was monitored after storage at 25 degrees C and 60% RH for up to 12 weeks. The flow-through method was found suitable as dissolution method. All SDs showed improved in-vitro dissolution rates when compared to starting material and physical mixtures. The greatest improvement in the in-vitro dissolution rate was observed for the highest polymer to drug ratio. By means of the results from XRPD and DSC, it was argued that the presence of amorphous probucol improved the dissolution rate, but the amorphous state could not fully account for the difference in dissolution profiles between the SDs. It was suggested that the increase in surface area due to the reduction in particle size contributed to an increased dissolution rate as well as the presence of PVP-K30 by preventing aggregation and drug re-crystallization and by improving wettability during dissolution. The stabilizing effect of the polymer was verified in the solid state, as all the SDs retained probucol in the amorphous state throughout the entire length of the stability study.
    Original languageEnglish
    JournalPharmaceutical Development and Technology
    Volume13
    Issue number5
    Pages (from-to)375-86
    Number of pages11
    ISSN1083-7450
    DOIs
    Publication statusPublished - 2008

    Bibliographical note

    Keywords: Anticholesteremic Agents; Chemistry, Pharmaceutical; Crystallization; Drug Stability; Drug Storage; Excipients; Humidity; Particle Size; Povidone; Powders; Probucol; Solubility; Wettability

    Keywords

    • Former Faculty of Pharmaceutical Sciences

    Cite this