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Anticancer drugs, controlled

Bontha, S., et al. (2006), Polymer micelles with cross-linked ionic cores for delivery of anticancer drugs,/. Controlled Release, 114(2), 163-174. [Pg.1311]

Collagen/ HEMA mixed with collagen and anticancer drugs Controlled release of Jeyanthi and Rao, 1990... [Pg.222]

The significance of P-gp, however, in affecting absorption and bioavailability of P-gp substrate drugs can be seen in studies in knockout mice that do not have intestinal P-gp. The gene responsible for producing that protein has been knocked out of the genetic repertoire. Those animals evidenced a sixfold increase in plasma concentrations (and AUC, area under the plasma concentration-time curve) of the anticancer drug paclitaxel (Taxol) compared to the control animals [54]. Another line of evidence is the recent report... [Pg.50]

CONTROLLING PLATINUM, RUTHENIUM, AND OSMIUM REACTIVITY FOR ANTICANCER DRUG DESIGN... [Pg.1]

Ultimately, for Pt(IV) anticancer drugs, a combination of incorporation of bioactive ligands that specifically target cancer cells, control over ligand-exchange kinetics, and selective activation by light would allow for temporal and spatial control of drug delivery and activation. [Pg.9]

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Anticancer drugs

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