Liposomal chemotherapy often suffers from structural instability and premature drug leakage in the bloodstream, leading to systemic toxicity and reduced tumor accumulation. Herein, we developed a robust biomimetic nanodelivery system (PDLC) designed to stabilize the lipid bilayer via a rigid polymer core. The PDLC was synthesized based on the strong molecular affinity between poly(L-lactic acid) and phospholipid monomer to form a molecular interlock that prevents premature drug leakage. The system comprises a DOX-loaded PLLA core, a lipid stabilization layer, and a 4T1 tumor cell membrane coating for homotypic targeting. PDLC effectively suppressed the initial burst release (<10% at 24 h) while exhibiting pH-responsive release in acidic tumor microenvironments. Facilitated by cell membrane-mediated endocytosis, PDLC showed enhanced uptake in 4T1 cells. In vivo imaging confirmed superior tumor homing capabilities, translating to a potent 80.1% tumor inhibition rate without the cardiotoxicity typical of free DOX. By mechanistically reinforcing lipid stability through polymer-lipid interactions, this study offers a compelling biomimetic strategy to maximize the therapeutic index of chemotherapeutic agents.
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Huang et al. (2026) studied this question.
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