Capture of stealth nanoparticles by the body's defences

S. M. Moghimi, A. C. Hunter

    Research output: Contribution to journalArticlepeer-review

    Abstract

    This article highlights and discusses our experience in the design, handling, and biological evaluation of long-circulating nanoparticles based on polyoxypropylene/polyoxyethylene copolymer nonionic surfactants. A frequently observed but ignored phenomenon following intravenous injection of such polymer-modified long-circulating colloidal systems is their eventual recognition and clearance by macrophages of the reticuloendothelial system. The pharmacokinetics as well as the tissue distribution of such so-called "stealth" nanoparticles are also altered after repeated intravenous injection in a time-dependent manner. An understanding of immunological and pathological factors that control the pharmacokinetic and biological behavior of long-circulating particles after single or repeated administration is therefore crucial for the design of a system with an optimal diagnostic and/or therapeutic performance. Therefore, we have also examined and discussed the concept of macrophage recognition of a "stealth-like nature" and factors that initiate this cascade. A critical discussion of the future of this interesting area of nano-biotechnology/engineering is also provided.
    Original languageEnglish
    Pages (from-to)527-550
    Number of pages23
    JournalCritical Reviews in Therapeutic Drug Carrier Systems
    Volume18
    Issue number6
    Publication statusPublished - 2001

    Keywords

    • Bone marrow sinus endothelial cells
    • Complement activation
    • Drug delivery systems
    • Kupffer cell
    • Liposomes
    • Liver endothelial cells
    • Long circulating nanoparticles
    • Macrophage
    • Macrophage activation
    • Opsonization
    • Phagocytosis
    • Poloxamer
    • Poloxamine
    • Spleen

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