Drug nanocrystallisation within liposomes

Tang Li, David Cipolla, Thomas Rades, Ben J. Boyd*

*Corresponding author af dette arbejde
    41 Citationer (Scopus)

    Abstract

    Liposomes are phospholipid bilayer vesicles that have been explored in pharmaceutical research as drug delivery systems for >50 years. Despite being important to their morphology and drug release pattern, the physical state of the drug within liposomes (liquid, solid, crystalline form) is often overlooked. This review focuses on precipitation of drug within liposomes, which can result in the formation of confined nanocrystals, and consequent changes in liposome morphology and drug release patterns. The type of drugs that form nanocrystals within liposomes, preparation and characterisation of liposomal drug nanocrystals, and the in vitro drug release behaviour from these systems are communicated, with a discussion of their potential as drug delivery systems.

    OriginalsprogEngelsk
    TidsskriftJournal of Controlled Release
    Vol/bind288
    Sider (fra-til)96-110
    Antal sider15
    ISSN0168-3659
    DOI
    StatusUdgivet - 2018

    Fingeraftryk

    Dyk ned i forskningsemnerne om 'Drug nanocrystallisation within liposomes'. Sammen danner de et unikt fingeraftryk.

    Citationsformater