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Cancer-targeted tri-block copolymer nanoparticles as payloads of metal complexes to achieve enhanced cancer theranosis
被引:26
作者:

Chan, Leung
论文数: 0 引用数: 0
h-index: 0
机构:
Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China

Huang, Yanyu
论文数: 0 引用数: 0
h-index: 0
机构:
Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China

Chen, Tianfeng
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h-index: 0
机构:
Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
机构:
[1] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
基金:
国家高技术研究发展计划(863计划);
关键词:
RATIONAL DESIGN;
DRUG-DELIVERY;
PLGA NANOPARTICLES;
CELLULAR UPTAKE;
NAMI-A;
RESISTANCE;
APOPTOSIS;
CELLS;
ACTIVATION;
NANOSYSTEM;
D O I:
10.1039/c6tb00514d
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
Cancer targeting delivery and controlled release of metal complexes may offer a new approach to improve their anticancer efficacy with eliminated systemic toxicities. Herein, a biotin-conjugated tri-block polymer delivery system was designed and used as a carrier of potent ruthenium polypyridyl (RuPOP) complexes to achieve superior biocompatibility, higher water solubility and cancer-targeting ability. Biotin was used as a targeting molecule to enhance the cellular uptake and retention of RuPOP in diverse carcinoma cells. Furthermore, the nanosystem (Bio-PLGA@Ru) was efficiently internalized by cancer cells by the lipid raft-mediated endocytosis pathway, triggered ROS overproduction and activated p53-mediated apoptosis in cancer cells. Moreover, the nanosystem effectively accumulated in tumor tissue and alleviated the damage of the metal complex to the organs. Taken together, this study demonstrates a smart strategy for the fabrication of a biocompatible and cancer-targeted PLGA-based copolymer nanosystem to achieve superior tumor cell localization and anticancer ability with eliminated systemic toxicities.
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页码:4517 / 4525
页数:9
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Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China

Zheng, Wen-Jie
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Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China

Liu, Jie
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Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China

Wong, Yum-Shing
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Chinese Univ Hong Kong, Dept Biol, Hong Kong, Hong Kong, Peoples R China Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China