Hyaluronic Acid-Functionalized Polydopamine Nanoparticles Augment Photothermal Therapy via Synergetic Tumor-Targeting and Heat Shock Protein Inhibition

被引:2
|
作者
Ruan, Lingyun [1 ]
Cao, Yuanyuan [2 ,3 ]
Ren, Caixia [2 ,3 ]
Li, Huan [1 ]
Feng, Xuesong [1 ]
Hao, Rongzhang [2 ,3 ]
机构
[1] China Med Univ, Sch Pharm, Shenyang 110122, Peoples R China
[2] Capital Med Univ, Sch Publ Hlth, Dept Toxicol & Sanit Chem, Beijing 100069, Peoples R China
[3] Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
photothermal therapy; polydopamine; hyaluronicacid; tumor targeting; heat shock protein; COVALENT ORGANIC FRAMEWORKS;
D O I
10.1021/acsanm.3c04655
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As an alternative or supplement to conventional tumor treatment, photothermal therapy (PTT) is a rapid development technique for tumor elimination with the advantages of remote manipulation and minimal invasiveness. Although many different nanomaterials used in PTT have achieved excellent tumor treatment effects, poor tumor accumulation and high tumor heat resistance might lead to low PTT efficacy and frequent tumor recurrence. Herein, a kind of tumor-targeting nanoparticle (PDA-HA/STA9090 NPs) was rationally designed through conjugating hyaluronic acid (HA) on the surface of polyamine (PDA), along with loading the heat shock protein 90 (HSP90) inhibitor Ganetespib (STA9090). The PDA-HA/ST9090 NPs not only presented a high photothermal conversion efficiency (35.2%) but also enhanced the accumulation in tumoral sites for efficient downregulation of HSP90 in vitro. Accordingly, the mice treated with PDA-HA/STA9090 NPs under 808 nm laser irradiation showed the most effective tumor inhibition. Taken together, this work could not only provide a potential strategy to reduce hyperthermia side effects but also prompt the therapeutic effect of PTT with the assistance of HSP inhibition.
引用
收藏
页码:20458 / 20468
页数:11
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