LAPONITE-Polyethylenimine Based Theranostic Nanoplatform for Tumor-Targeting CT Imaging and Chemotherapy

被引:47
作者
Zhuang, Ying [1 ]
Zhou, Lingzhou [2 ]
Zheng, Linfeng [2 ]
Hu, Yong [1 ]
Ding, Ling [1 ]
Li, Xin [1 ]
Liu, Changcun [2 ]
Zhao, Jinhua [2 ]
Shi, Xiangyang [1 ,3 ]
Guo, Rui [1 ]
机构
[1] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
[2] Shanghai Jiao Tong Univ, Peoples Hosp 1, Dept Radiol, 100 Haining Rd, Shanghai 20080, Peoples R China
[3] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
来源
ACS BIOMATERIALS SCIENCE & ENGINEERING | 2017年 / 3卷 / 03期
基金
中国国家自然科学基金;
关键词
laponite; gold nanoparticles; hyaluronic acid targeting; CT imaging; chemotherapy; ENTRAPPED GOLD NANOPARTICLES; ANTICANCER DRUG-DELIVERY; IRON-OXIDE NANOPARTICLES; CANCER-CELLS; MESOPOROUS SILICA; FOLIC-ACID; IN-VITRO; PHOTOTHERMAL THERAPY; FACILE SYNTHESIS; HYALURONIC-ACID;
D O I
10.1021/acsbiomaterials.6b00528
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
In this study, laponite (LAP) nanodisks and polyethylenimine (PEI) were used to build a hybrid theranostic nanoplatform for targeted computed tomography (CT) imaging and chemotherapy of cancer cells overexpressing CD44 receptors. First, amphiphilic copolymer poly(lactic acid)poly(ethylene glycol) (PLA-PEG-COOH) were assembled on the surface of LAP nanodisks via hydrophobic interaction, and 100 then PEI were conjugated by the formation of amide groups vial-ethyl-3-(3-(dimethylamino)propyl) carbodiimide (EDC) coupling chemistry. The developed LAP-PLA-PEG-PEI nano-particles were used as templates for the embedding of gold nanoparticles (Au NPs), followed by modification with hyaluronic acid (HA) as a targeting ligand for cancer cells overexpressing CD44 receptors. Finally, anticancer drug doxorubicin (DOX) was loaded. The formed LAP-PLA-PEG-PEI-(Au-0)(50)-HA/DOX nanocomplexes display good stability, a high drug loading efficiency as 91.0 +/- 1.8%, and sustained drug release profile with a pH -sensitive manner. In vitro cell viability assay, flow cytometric analysis, and laser scanning confocal microscopy observation demonstrate that the formed nanocomplexes can specifically deliver and inhibit cancer cells overexpressing CD44 receptors. In vivo experiments illustrate that LAP-PLA-PEGPEI-(Au-0)(50)-HA/DOX nanocomplexes can not only significantly inhibit the growth of tumors and decrease the side -effect of DOX, but also be used as a targeted contrast agent for CT imaging of tumors. Therefore, the developed LAP-PLA-PEG-PEI-(Au-0)(50)-HA/DOX nanocomplexes can be used as a promising theranostic platform for targeted imaging and chemotherapy of CD44-overexpressed tumors.
引用
收藏
页码:431 / 442
页数:12
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