The pharmacology and clinical use of caspofungin

William W. Hope, Shmuel Shoham, Thomas J. Walsh

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Caspofungin was the first echinocandin to be licensed for the treatment of invasive fungal infections. Caspofungin has in vitro and in vivo activity against Candida spp. and Aspergillus spp., which constitute the majority of medically important opportunistic fungal pathogens. Caspofungin inhibits the synthesis of the 1,3-β-glucan, with resultant osmotic instability and lysis. The pharmacology of caspofungin is relatively complex. Trafficking of drug into tissues is an important determinant of the shape of the concentration-time relationship. Caspofungin has demonstrated efficacy in experimental models of invasive candidiasis and aspergillosis, which reflect its activity in the treatment of oropharyngeal, esophageal and disseminated candidiasis, as well as salvage therapy for patients with invasive aspergillosis. © 2007 Informa UK Ltd.
    Original languageEnglish
    Pages (from-to)263-274
    Number of pages11
    JournalExpert Opinion on Drug Metabolism and Toxicology
    Volume3
    Issue number2
    DOIs
    Publication statusPublished - Apr 2007

    Keywords

    • Aspergillus
    • Candida
    • Caspofungin
    • Echinocandin
    • Glucan
    • Pharmacodynamics
    • Pharmacokinetics

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