Modulating Intracellular Dynamics for Optimized Intracellular Release and Transcytosis Equilibrium

Active transcytosis-mediated nanomedicine transport presents considerable potential in overcoming diverse delivery barriers, thereby facilitating tumor accumulation and penetration. Nevertheless, the persistent challenge lies in achieving a nuanced equilibrium between intracellular interception for drug release and transcytosis for tumor penetration. In this study, a comprehensive exploration is conducted involving a series of polyglutamine-paclitaxel conjugates featuring distinct hydrophilic/hydrophobic ratios (HHR) and tertiary amine-oxide proportions (TP) (OPGA-PTX). The screening process, meticulously focused on delineating their subcellular distribution, transcytosis capability, and tumor penetration, unveils a particularly promising candidate denoted as OPPX, characterized by an HHR of 10:1 and a TP of 100%. OPPX, distinguished by its rapid cellular internalization through multiple endocytic pathways, selectively engages in trafficking to the Golgi apparatus for transcytosis to facilitate accumulation within and penetration throughout tumor tissues and simultaneously sorted to lysosomes for cathepsin B-activated drug release. This study not only identifies OPPX as an exemplary nanomedicine but also underscores the feasibility of modulating subcellular distribution to optimize the active transport capabilities and intracellular release mechanisms of nanomedicines, providing an alternative approach to designing efficient anticancer nanomedicines. A comprehensive investigation into polyglutamine-paclitaxel conjugates with varying hydrophilic/hydrophobic ratios and tertiary amine-oxide proportions aims (OPGA-PTX) to optimize an equilibrium between intracellular interception and transcytosis behaviors. OPPX emerges as a superior candidate, demonstrating selective trafficking to the Golgi apparatus for transcytosis and lysosomal sorting for cathepsin B-activated drug release, thereby achieving enhanced tumor penetration and efficient antitumor activity. image