Synthesis and biological evaluation of redox/NIR dual stimulus-responsive polymeric nanoparticles for targeted delivery of cisplatin

被引:26
作者
You, Chaoqun [1 ]
Wu, Hongshuai [1 ]
Wang, Minxing [1 ]
Gao, Zhiguo [1 ]
Sun, Baiwang [1 ]
Zhang, Xiangyang [2 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 210089, Jiangsu, Peoples R China
[2] Swiss Fed Inst Technol, Lab Organ Chem, CH-8093 Zurich, Switzerland
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2018年 / 92卷
基金
中国国家自然科学基金;
关键词
Cisplatin; Dual targets; Redox stimulus-response; Photothermal conversion; Polymeric nanoparticles; Core-crosslinking; INFRARED PHOTOTHERMAL THERAPY; DRUG-DELIVERY; TRIGGERED RELEASE; POLYPYRROLE NANOPARTICLES; INTRACELLULAR DELIVERY; SUSTAINED DELIVERY; COPOLYMER MICELLES; BLOCK-COPOLYMERS; CANCER-THERAPY; IN-VITRO;
D O I
10.1016/j.msec.2018.06.044
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
Functional drug delivery systems enabling various favorable characteristics including specific targets, efficient cellular uptake and controllable release. At present work, a folate and cRGD dual modified nanoparticles based on NIR light and glutathione dual stimuli-responsive release system was successfully prepared and which simultaneously deliver cisplatin and ICG to tumor sites to enhance controllability. The prepared nanoparticles showed a stable uniform spherical morphology of 77.59 nm particle size range in PBS (pH = 7.4, 25 degrees C) and the encapsulated cisplatin were rapidly released in acidic environment especially added glutathione (GSH) and NIR irradiation. Moreover, the prepared nanoparticles can be efficiently internalized by tumor cells through the enhanced dual targeted ligands (folate and cRGD) for ICG imaging. The cytotoxicity assays showed that the cells viability decreased to 1.95% (SGC-7901) when been exposed to NIR light, and which further decreased to 1.25% in MCF-7 cells. Thus, the prepared nanoparticles showed excellent performance for photothermal conversion therapy of tumor cells and especially on human breast tumor cells. Our research highlights the great potential of stimuli-responsive smart nanoparticles in biomaterial and nano-biomedicine.
引用
收藏
页码:453 / 462
页数:10
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