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 language | English |
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Pages (from-to) | 527-550 |
Number of pages | 23 |
Journal | Critical Reviews in Therapeutic Drug Carrier Systems |
Volume | 18 |
Issue number | 6 |
Publication status | Published - 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