Light-Triggered Biomimetic Nanoerythrocyte for Tumor-Targeted Lung Metastatic Combination Therapy of Malignant Melanoma

被引:120
作者
Liu, Wen [1 ]
Ruan, Miaoliang [1 ]
Wang, Yanming [1 ]
Song, Rongguang [1 ]
Ji, Xin [1 ]
Xu, Jiake [2 ]
Dai, Jian [1 ]
Xue, Wei [1 ,3 ,4 ]
机构
[1] Jinan Univ, Dept Biomed Engn, Key Lab Biomat, Guangdong Higher Educ Inst, Guangzhou 510632, Guangdong, Peoples R China
[2] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA 6009, Australia
[3] Jinan Univ, Guangdong Higher Educ Inst, Inst Life & Hlth Engn, Key Lab Funct Prot Res, Guangzhou 510632, Guangdong, Peoples R China
[4] Jinan Univ, Affiliated Hosp 1, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
biomimetic nanoparticle; chemophototherapy; RBC membrane; targeted delivery; DRUG-DELIVERY; CELL-MEMBRANE; PHOTODYNAMIC THERAPY; CANCER; NANOPARTICLES; CHALLENGES; BLOCKADE; THERAPEUTICS; VACCINATION; BARRIERS;
D O I
10.1002/smll.201801754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Red blood cell (RBC) membrane-cloaked nanoparticles, reserving the intact cell membrane structure and membrane protein, can gain excellent cell-specific functions such as long blood circulation and immune escape, providing a promising therapy nanoplatform for drug delivery. Herein, a novel RBC membrane biomimetic combination therapeutic system with tumor targeting ability is constructed by embedding bovine serum albumin (BSA) encapsulated with 1,2-diaminocyclohexane-platinum (II) (DACHPt) and indocyanine green (ICG) in the targeting peptide-modified erythrocyte membrane (R-RBC@BPtI) for enhancing tumor internalization and synergetic chemophototherapy. R-RBC@BPtI displays excellent stability and high encapsulation efficiency with multiple cores enveloped in the membrane. Benefited from the stealth functionality and targeting modification of erythrocyte membranes, R-RBC@BPtI can significantly promote tumor targeting and cellular uptake. Under the near-infrared laser stimuli, R-RBC@BPtI presents remarkable instability by singlet oxygen and heat-mediated cleavage so as to trigger effective drug release, thereby achieving deep penetration and accumulation of DACHPt and ROS in the tumor site. Consequently, R-RBC@BPtI with tumor-specific targeting ability accomplishes remarkable ablation of tumors and suppressed lung metastasis in vivo by photothermal and chemotherapy combined ablation under phototriggering. This research provides a novel strategy of targeted biomimetic nanoplatforms for combined cancer chemotherapy-phototherapy.
引用
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页数:15
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