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Preparation of solid dispersion with respect to the dissolution rate of active substance

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F19%3A43919584" target="_blank" >RIV/60461373:22310/19:43919584 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sheffield.ac.uk/agglom/2019/index#" target="_blank" >https://www.sheffield.ac.uk/agglom/2019/index#</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Preparation of solid dispersion with respect to the dissolution rate of active substance

  • Original language description

    Solid dispersions (SDs) are one of widely and successfully applied methods to improve the solubility, dissolution rates and the bioavailability of poorly water-soluble drugs. SDs are commonly binary API-polymer systems, where API is molecularly dispersed in a polymeric matrix. Thus, the objective of this study was to prepare SDs by solvent evaporation and spray drying method and compare them with the physical mixtures (PMs) in terms of dissolution properties. Tadalafil was used as a model poorly water-soluble drug, which was mixed with three different hydrophilic polymer matrices, Kollidon® VA 64, Kollidon® 12 PF and Soluplus®. It was confirmed that hydrophilic polymers have a significant influence on the drug release from binary mixtures (SDs or PMs). The type of hydrophilic polymer can control if the drug release is either immediate or prolonged. Our results show that as the molecular weight of polymer increased, hydrophilic polymer more swollen and on the contrary, the drug release decreased. In this case of SDs, it means, that the presence of both Kollidons has a positive effect on the acceleration of tadalafil release, on the other hand, the presence of Soluplus® retarded its release. These results indicate possibility of different applications of SDs in pharmaceutical formulation, based on careful selection of the polymer co-former.

  • Czech name

  • Czech description

Classification

  • Type

    A - Audiovisual production

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • ISBN

  • Place of publication

  • Publisher/client name

  • Version

  • Carrier ID