https://flt-3inhibitors.com/in....dex.php/combination-
In this study, we created a couple of book dually hydrophobic prodrugs (DHPs) by incorporating two hydrophobic compounds through various linkers and elaborated their particular self-assembly mechanisms by virtue of computational simulation. Significantly, without the need for any excipients, FL-2 NPs exhibited significantly prolonged retention in the circulation of blood and displayed a remarkable anti-tumor impact at very low concentration in vivo.
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