A champagne inspired dual chain-responsive thrombolytic drug release platform based on black phosphorus nanosheets for accelerated thrombolysis

被引:23
作者
Ding, Xingwei [1 ]
Hong, Can [1 ,2 ]
Zhang, Guoliang [3 ]
Liu, Jiaqi [2 ]
Ouyang, Huan [3 ]
Wang, Manyu [2 ]
Dong, Lina [1 ]
Zhang, Wei [4 ]
Xin, Hongbo [1 ]
Wang, Xiaolei [1 ]
机构
[1] Nanchang Univ, Natl Engn Res Ctr Bioengn Drugs & Technol, Inst Translat Med, Nanchang 330088, Jiangxi, Peoples R China
[2] Nanchang Univ, Coll Pharm, Nanchang 330088, Jiangxi, Peoples R China
[3] Nanchang Univ, Coll Clin Med, Nanchang 330088, Jiangxi, Peoples R China
[4] Nanchang Univ, Coll Chem, Nanchang 330088, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
SEMICONDUCTING POLYMER; THROMBUS; NANOPARTICLES; ACTIVATION;
D O I
10.1039/c9nh00344d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To face the clinical challenges related to thrombolytic drugs, such as short blood circulation time, the large dosage required and the side effects of bleeding, the fabrication of a smart controlled thrombolytic drug release nano-system for physical assistant thrombolysis would be very significant. Inspired by champagne, an integrated chain-responsive thrombolytic drug delivery system, uPA@black phosphorus nanosheets-perfluoro-n-pentane@mesoporous silica nanoparticles (uPA@BPNs-PFP@MSNs) was fabricated as a multifunctional platform. The dual chain-responsive thrombolytic drug delivery platform, is first triggered by the photothermic effect of the black phosphorus nanosheets using near-infrared (NIR) laser irradiation (808 nm, 0.2 W cm(-2)), followed by accelerated thrombolytic drug release and the generation of bubbles from the phase change of the material. This platform was integrated via electrostatic adsorption and the thrombolysis, stability and cytocompatibility in vitro were assessed. Additionally, a murine acute jugular vein thrombosis model was built to evaluate the thrombolysis, biosafety and distribution in vivo. In light of these results, the platform has potential applications for delivering thrombolytic drugs safely and accelerating thrombolysis with a reduced dose of drugs clinically.
引用
收藏
页码:1277 / 1285
页数:9
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