Amorphous drugs and dosage forms

Holger Grohganz, K. Löbmann, P. Priemel, Katrine Birgitte Tarp Jensen, K. Graeser, C. Strachan, T. Rades

    36 Citationer (Scopus)

    Abstract

    The transformation to an amorphous form is one of the most promising approaches to address the low solubility of drug compounds, the latter being an increasing challenge in the development of new drug candidates. However, amorphous forms are high energy solids and tend to recry stallize. New formulation principles are needed to ensure the stability of amorphous drug forms. The formation of solid dispersions is still the most investigated approach, but additional approaches are desirable to overcome the shortcomings of solid dispersions. Spatial separation by either coating or the use of micro-containers has shown potential to prevent or delay recrystallization. Another recent approach is the formation of co-amorphous mixtures between either two drugs or one drug and one low molecular weight excipient. Molecular interactions between the two molecules provide an energy barrier that has to be overcome before single molecules are available for the formation of crystal nuclei, thus stabilizing the amorphous form.
    OriginalsprogEngelsk
    TidsskriftJournal of Drug Delivery Science and Technology
    Vol/bind23
    Udgave nummer4
    Sider (fra-til)403-408
    Antal sider6
    ISSN1773-2247
    StatusUdgivet - 1 jul. 2013

    Fingeraftryk

    Dyk ned i forskningsemnerne om 'Amorphous drugs and dosage forms'. Sammen danner de et unikt fingeraftryk.

    Citationsformater