Tumor-Specific ONOO- Nanogenerator for Improved Drug Delivery and Enhanced Chemotherapy of Tumor

被引:50
作者
Chen, Ying [1 ,2 ]
Li, Zi-Hao [1 ,2 ]
Pan, Pei [1 ,2 ]
Zeng, Run-Yao [1 ,2 ]
Zhang, Xian-Zheng [1 ,2 ]
机构
[1] Wuhan Univ, Key Lab Biomed Polymers, Minist Educ, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
peroxynitrite; nanogenerator; drug delivery; tumor treatment; chemotherapy; MATRIX METALLOPROTEINASES; SODIUM-NITROPRUSSIDE; PEROXYNITRITE; CISPLATIN; NANOPARTICLES; NANOMEDICINE; PERMEABILITY; PENETRATION; ACTIVATION; RELEASE;
D O I
10.1021/acsnano.1c01312
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multiple biological barriers in solid tumors severely restrict the penetration of nanomedicines, which is a main cause for therapeutic failure in traditional tumor treatment. Here, a tumor-specific nanogenerator of peroxynitrite (ONOO-), prepared by loading cisplatin and sodium nitroprusside into poly(D,L-lactide-co-glycolide) polymersomes, was designed to improve drug delivery and enhance tumor chemotherapy. After a cascade of nicotinamide adenine dinucleotide phosphate oxidases catalysis and glutathione reduction, the nanogenerator, namely, PMCS, could selectively induce the generation of ONOO- in tumor. The generated ONOO- could not only strengthen vascular permeability significantly but also improve the accumulation and penetration of PMCS in tumor by activating matrix metalloproteinases-mediated degradation of extracellular matrix. Along with endocytosis, PMCS released cisplatin to induce tumor cell apoptosis. Moreover, free cisplatin liberated from dead cells infected neighboring tumor cells quickly via ONOO--mediated up-regulated copper transporter 1, further amplifying chemotherapeutic efficacy. This study advances ONOO- as a potent modality to address the main issues of therapeutic delivery, including but not limited to chemotherapy.
引用
收藏
页码:11514 / 11525
页数:12
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