Abstract
LIPOSOMES have been used as vehicles for transporting drugs or enzymes into cultured cells and into tissues1–8. Before the full potential of liposome delivery systems can be realised, however, means must be found to direct the drug or enzyme bearing particles to specific sites within the body. Some modulation of the in vivo distribution of liposomes can be achieved by altering the size or charge of the vesicles9,10. More precise control of the interaction of liposomes with cells, and their distribution in vivo, may, however, be possible through the introduction of specific macromolecular entities into the liposome membrane. As a preliminary step in this direction we have incorporated a macromolecular lectin receptor into liposome membranes and have examined the lectin-mediated attachment of such liposomes to cells in vitro.
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JULIANO, R., STAMP, D. Lectin-mediated attachment of glycoprotein-bearing liposomes to cells. Nature 261, 235–238 (1976). https://doi.org/10.1038/261235a0
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DOI: https://doi.org/10.1038/261235a0
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