A Versatile Polymer Micelle Drug Delivery System for Encapsulation and <i>In Vivo</i> Stabilization of Hydrophobic Anticancer Drugs

<table>Pharmacokinetics of daunorubicin-loaded micelles in rats. Sprague-Dawley rats were given a single intravenous administration of crosslinked daunorubicin micelle, uncrosslinked daunorubicin micelle, or free daunorubicin at a 10 mg/kg dose. Plasma was analyzed for daunorubicin concentration at various timepoints. The table depicts the area under curve (AUC) and <svg height="14.4375" id="M10" style="vertical-align:-3.22282pt" version="1.1" viewbox="0 0 33.724998 14.4375" width="33.724998" xmlns="http://www.w3.org/2000/svg">
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Journal of Drug Delivery

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Figure 5

Figure 5: A Versatile Polymer Micelle Drug Delivery System for Encapsulation and <i>In Vivo</i> Stabilization of Hydrophobic Anticancer Drugs 

Journal of Drug Delivery

A Versatile Polymer Micelle Drug Delivery System for Encapsulation and In Vivo Stabilization of Hydrophobic Anticancer Drugs

Figure 5