Light-Driven Self-Recruitment of Biomimetic Semiconducting Polymer Nanoparticles for Precise Tumor Vascular Disruption

© 2023 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 35(2023), 24 vom: 04. Juni, Seite e2210920
1. Verfasser: Li, Haoze (VerfasserIn)
Weitere Verfasser: Zhou, Sensen, Wu, Min, Qu, Rui, Wang, Xin, Chen, Weizhi, Jiang, Yuyan, Jiang, Xiqun, Zhen, Xu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article biomimetic semiconducting polymer nanoparticles light-driven self-recruitment reversion of immunosuppression tumor vascular disruption Polymers
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520 |a Tumor vascular disrupting therapy has offered promising opportunities to treat cancer in clinical practice, whereas the overall therapeutic efficacy is notably limited due to the off-target effects and repeated dose toxicity of vascular disrupting agents (VDAs). To tackle this problem, a VDA-free biomimetic semiconducting polymer nanoparticle (SPNP ) is herein reported for precise tumor vascular disruption through two-stage light manipulation. SPNP consists of a semiconducting polymer nanoparticle as the photothermal agent camouflaged with platelet membranes that specifically target disrupted vasculature. Upon the first photoirradiation, SPNP administered in vivo generates mild hyperthermia to trigger tumor vascular hemorrhage, which activates the coagulation cascade and recruits more SPNP to injured blood vessels. Such enhanced tumor vascular targeting of photothermal agents enables intense hyperthermia to destroy the tumor vasculature during the second photoirradiation, leading to complete tumor eradication and efficient metastasis inhibition. Intriguingly, the mechanism study reveals that this vascular disruption strategy alleviates splenomegaly and reverses the immunosuppressive tumor microenvironment by reducing myeloid-derived suppressor cells. Therefore, this study not only illustrates a light-driven self-recruitment strategy to enhance tumor vascular disruption via a single dose of biomimetic therapeutics but also deciphers the immunotherapeutic role of vascular disruption therapy that is conducive to clinical studies 
650 4 |a Journal Article 
650 4 |a biomimetic semiconducting polymer nanoparticles 
650 4 |a light-driven self-recruitment 
650 4 |a reversion of immunosuppression 
650 4 |a tumor vascular disruption 
650 7 |a Polymers  |2 NLM 
700 1 |a Zhou, Sensen  |e verfasserin  |4 aut 
700 1 |a Wu, Min  |e verfasserin  |4 aut 
700 1 |a Qu, Rui  |e verfasserin  |4 aut 
700 1 |a Wang, Xin  |e verfasserin  |4 aut 
700 1 |a Chen, Weizhi  |e verfasserin  |4 aut 
700 1 |a Jiang, Yuyan  |e verfasserin  |4 aut 
700 1 |a Jiang, Xiqun  |e verfasserin  |4 aut 
700 1 |a Zhen, Xu  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 35(2023), 24 vom: 04. Juni, Seite e2210920  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnns 
773 1 8 |g volume:35  |g year:2023  |g number:24  |g day:04  |g month:06  |g pages:e2210920 
856 4 0 |u http://dx.doi.org/10.1002/adma.202210920  |3 Volltext 
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