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Polymer dextran-doxorubicin

The hydrophilic delivery system described in this review can be extended to drugs with a low water-solubility (e.g., doxorubicin). Such compounds may be incorporated in CT/TPP nanoparticles by means of dextran sulfate complex prior to entrapment [54] or by dissolving them in a polar solvent (acetone, ethanol or acetonitrile) as demonstrated for the relatively hydrophobic peptide cyclosporin A [26,81]. It is quite possible that this approach would work in a multicomponent polymer system as well. [Pg.167]

See other pages where Polymer dextran-doxorubicin is mentioned: [Pg.37]    [Pg.37]    [Pg.792]    [Pg.291]    [Pg.130]    [Pg.1184]    [Pg.7]    [Pg.286]    [Pg.162]    [Pg.210]    [Pg.6364]    [Pg.230]    [Pg.7]    [Pg.1460]   
See also in sourсe #XX -- [ Pg.37 ]

See also in sourсe #XX -- [ Pg.37 ]



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