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Self-assembled nano-multiple warheads: A precise targeting platform for combinatorial chemotherapy, PTT and PDT therapy against glioma

Journal 2026 · IF 6.7 · 发表于 2026 年 8 月 25 日
作者: Zhihao Chen,Mengru Wu,Qianwen Ren,Wanjun Liang,Xiu Wang
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摘要

DIPF was fabricated via drug self-assembly, with high encapsulation efficiency and loading capacity of both DOX and ICG. • DIPF exhibits strong ability to penetrate the BBB, to accumulate in gliomas, and enables real-time in vivo imaging. • DIPF integrates chemotherapy, PTT and PDT to inhibit gliomas, overcome drug resistance and reduce DOX-induced cardiotoxicity. • DIPF is a promising delivery platform for multi‑therapy glioma treatment. Combination therapy tactics that incorporate numerous therapies via innovative multi-drug co-loaded nanomedicine delivery systems have shown considerable benefits in crossing the blood-brain barrier (BBB) and slowing glioma growth. However, efficiently developing multi-drug co-loaded delivery systems with high drug loading capacity, the ability to alleviate drug resistance, and minimal in vivo toxicity remains a significant problem. In this study, we created a self-assembling nanomedicine delivery system using a DIPF composite encapsulated with polydopamine and folate. The nanoparticles have an internally coated self-assembled structure that is assembled via electrostatic interactions, π-π stacking, and hydrophobic interactions between doxorubicin (DOX) and indocyanine green (ICG). This achieves high encapsulation efficiency and loading content for the co-delivery of multiple drugs. In this delivery system, the encapsulation efficiencies of DOX and ICG reached 94.08% and 94.01%, respectively, while the inherent cardiotoxicity of DOX was reduced by 64.33%. H&E staining results and anti-tumor experimental outcomes—including expression of TNF-α, Ki67, Caspase-3, and GFAP cytokines—clearly demonstrated that combined DIPF+NIR therapy significantly inhibited tumor growth and substantially extended survival. The highly efficient multi-drug co-loaded delivery system developed here demonstrates significant application potential for active targeting, controlled drug release, treatment visualization, and combined chemotherapy, photothermal (PTT), and photodynamic (PDT) therapy for brain tumors. A highly efficient multi-drug co-loaded drug delivery system that can cross the BBB and delivery combined chemotherapy, photothermal and photodynamic therapy for brain tumors target was established in a self-assembling way via electrostatic interactions, π-π stacking, and hydrophobic interactions between doxorubicin and indocyanine green. Download: Download high-res image (202KB) Download: Download full-size image

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