Luminescent/magnetic PLGA-based hybrid nanocomposites: a smart nanocarrier system for targeted codelivery and dual-modality imaging in cancer theranostics

被引:47
作者
Shen, Xue [1 ]
Li, Tingting [1 ]
Chen, Zhongyuan [1 ]
Geng, Yue [1 ]
Xie, Xiaoxue [1 ]
Li, Shun [1 ,2 ]
Yang, Hong [1 ,2 ]
Wu, Chunhui [1 ,2 ]
Liu, Yiyao [1 ,2 ]
机构
[1] Univ Elect Sci & Technol China, Sch Life Sci & Technol, Dept Biophys, Chengdu 610054, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Ctr Informat Biol, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
doxorubicin; codelivery; dual-modality imaging; synergistic antitumor effects; VEGF shRNA; IRON-OXIDE NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; MAGNETIC FE3O4 NANOPARTICLES; CO-DELIVERY; TUMOR-GROWTH; FOLIC-ACID; DRUG-DELIVERY; BREAST-CANCER; SUPERPARAMAGNETIC NANOPARTICLES; BIOMEDICAL APPLICATIONS;
D O I
10.2147/IJN.S136766
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cancer diagnosis and treatment represent an urgent medical need given the rising cancer incidence over the past few decades. Cancer theranostics, namely, the combination of diagnostics and therapeutics within a single agent, are being developed using various anticancer drug-, siRNA-, or inorganic materials-loaded nanocarriers. Herein, we demonstrate a strategy of encapsulating quantum dots, superparamagnetic Fe3O4 nanocrystals, and doxorubicin (DOX) into biodegradable poly(D,L-lactic-co-glycolic acid) (PLGA) polymeric nanocomposites using the double emulsion solvent evaporation method, followed by coupling to the amine group of polyethyleneimine premodified with polyethylene glycol-folic acid (PEI-PEG-FA [PPF]) segments and adsorption of vascular endothelial growth factor (VEGF)-targeted small hairpin RNA (shRNA). VEGF is important for tumor growth, progression, and metastasis. These drug-loaded luminescent/magnetic PLGA-based hybrid nanocomposites (LDM-PLGA/PPF/VEGF shRNA) were fabricated for tumor-specific targeting, drug/gene delivery, and cancer imaging. The data showed that LDM-PLGA/PPF/VEGF shRNA nanocomposites can codeliver DOX and VEGF shRNA into tumor cells and effectively suppress VEGF expression, exhibiting remarkable synergistic antitumor effects both in vitro and in vivo. The cell viability was similar to 14% when treated with LDM-PLGA/PPF/VEGF shRNA nanocomposites ([DOX] =25 mu g/mL), and in vivo tumor growth data showed that the tumor volume decreased by 81% compared with the saline group at 21 days postinjection. Magnetic resonance and fluorescence imaging data revealed that the luminescent/magnetic hybrid nanocomposites may also be used as an efficient nanoprobe for enhanced T-2-weighted magnetic resonance and fluorescence imaging in vitro and in vivo. The present work validates the great potential of the developed multifunctional LDM-PLGA/PPF/VEGF shRNA nanocomposites as effective theranostic agents through the codelivery of drugs/genes and dual-modality imaging in cancer treatment.
引用
收藏
页码:4299 / 4322
页数:24
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