Red blood cell membrane-coated functionalized Au nanocage as a biomimetic platform for improved MicroRNA delivery in hepatocellular carcinoma

被引:15
作者
Huang, Shengnan [1 ,2 ]
Song, Chengzhi [3 ]
Miao, Jinxin [1 ]
Zhu, Xiali [4 ]
Jia, Yongyan [4 ]
Liu, Yafei [2 ]
Fu, Dongjun [5 ]
Li, Benyi [6 ]
Miao, Mingsan [1 ]
Duan, Shaofeng [7 ]
Zhang, Zhenzhong [2 ]
Hu, Yurong [2 ,8 ]
机构
[1] Henan Univ Chinese Med, Acad Chinese Med Sci, Zhengzhou 450046, Henan, Peoples R China
[2] Zhengzhou Univ, Sch Pharmaceut Sci, Key Lab Targeting Therapy & Diag Crit Dis, Zhengzhou 450001, Henan, Peoples R China
[3] Peking Univ, Ctr Quantitat Biol, Beijing 100871, Peoples R China
[4] Henan Univ Chinese Med, Sch Pharmaceut Sci, Zhengzhou 450046, Henan, Peoples R China
[5] Beijing Univ Chinese Med, Beijing Res Inst Chinese Med, Beijing 100029, Peoples R China
[6] Univ Kansas, Dept Urol, Med Ctr, Kansas City, KS 66160 USA
[7] Henan Univ, Sch Pharm, Henan Int Joint Lab Chinese Med Efficacy, Kaifeng 475004, Henan, Peoples R China
[8] Zhengzhou Univ, Sch Pharmaceut Sci, 100 Kexue Ave, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Red blood cell membrane; microRNA delivery; Au nanocage; Cellular uptake; Prolonged circulation time; Accelerated blood clearance; GOLD NANOCAGES; DRUG-DELIVERY; LONG CIRCULATION; NANOPARTICLES; CLEARANCE; TUMOR; THERAPY; PEG; NANOMATERIALS; LIPOSOMES;
D O I
10.1016/j.ijpharm.2023.123044
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dysregulation of microRNAs (miRNAs) expression is closely related to cancers and managing miRNA expression holds great promise for cancer therapy. However, their wide clinical application has been hampered by their poor stability, short half-life and non-specific biodistribution in vivo. Herein, a novel biomimetic platform designated as RHAuNCs-miRNA for improved miRNA delivery was prepared through wrapping miRNA-loaded functionalized Au nanocages (AuNCs) with red blood cell (RBC) membrane. RHAuNCs-miRNA not only successfully loaded miRNAs but also effectively protected them from enzymatic degradation. With good stability, RHAuNCs-miRNA had the characteristics of photothermal conversion and sustained release. Cellular uptake of RHAuNCs-miRNA by SMMC-7721 cells was in a time-dependent manner via clathrin- and caveolin-mediated endocytosis. The uptake of RHAuNCs-miRNAs was affected by cell types and improved by mild near infrared (NIR) laser irradiation. More importantly, RHAuNCs-miRNA exhibited a prolonged circulation time without the occurrence of accelerated blood clearance (ABC) in vivo, resulting in efficient delivery to tumor tissues. This study may demonstrate the great potential of RHAuNCs-miRNA for improved miRNAs delivery.
引用
收藏
页数:12
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