An in vitro study of the diclofenac delivery properties of hyaluronan in human skin

G P Martin, Marc Brown, F C Bennett, C. Marriott

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    4 Citations (Scopus)

    Abstract

    Previous in vitro studies have indicated that hyaluronan, when compared to buffer controls, effects a controlled and sustained release of diclofenac through the skin by the formation of a reservoir of the drug around the basement membrane. The aim of this study was to further characterize the drug delivery properties of hyaluronan by comparing it with other gel-forming materials and another glycosaminoglycan, chondroitin sulphate. The results show that neither NaCMC (at a weight or theologically equivalent concentration) nor chondroitin sulphate (at a weight equivalent concentration) exert the controlled release effect seen for the hyaluronan formulation in full thickness skin. A significant difference is seen between the cumulative amounts of labelled diclofenac diffused from the controls at times where sink conditions for the hyaluronan formulation are reached (p less than or equal to 0.05). Mass balance calculations from each experiment show that significantly more activity is retained in the skin when applied in 2.5% HA, compared to 2.5% NaCMC (p less than or equal to 0.02), 3.2% NaCMC (p less than or equal to 0.05) and 2.5% chondroitin sulphate (p less than or equal to 0.02). This study supports the hypothesis that the controlled release and epidermal retention of diclofenac is a characteristic specific to the hyaluronan formulation and does not appear to be observed with another theologically equivalent gel, such as NaCMC or an alternative glycosaminoglycan, chondroitin sulphate.

    Original languageEnglish
    Pages (from-to)39-43
    Number of pages5
    JournalJournal of Drug Delivery Science and Technology
    Volume6
    Issue number1
    Publication statusPublished - 1999

    Keywords

    • diclofenac
    • drug delivery
    • hyaluronan
    • hyaluronic acid
    • skin
    • topical
    • IN-VITRO
    • ANGIOGENESIS
    • COMBINATION
    • PENETRATION

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