Abstract
The development of liposomes targeted to angiogenic endothelial cells offers exciting prospects for intervention in cancer and inflammation. Several proteins are (strongly) over-expressed on angiogenic endothelial cells as compared to the quiescent endothelium, and could potentially serve as targets for site-specific drug delivery. In this contribution particular attention is given to the design of targeted long-circulating liposomes directed against the alpha v beta 3-integrin protein.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cells, Cultured
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Doxorubicin / pharmacology
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Endothelium, Vascular / cytology
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Humans
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Inflammation
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Integrin alphaVbeta3 / metabolism
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Integrins / metabolism
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Ligands
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Liposomes / metabolism*
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Neovascularization, Pathologic / drug therapy*
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Oligopeptides / pharmacology
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Polyethylene Glycols / metabolism
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Umbilical Veins / cytology
Substances
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Integrin alphaVbeta3
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Integrins
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Ligands
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Liposomes
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Oligopeptides
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Polyethylene Glycols
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arginyl-glycyl-aspartic acid
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Doxorubicin