PEGylated polydopamine-coated magnetic nanoparticles for combined targeted chemotherapy and photothermal ablation of tumour cells

被引:55
作者
Xue, Peng [1 ,2 ]
Sun, Lihong [1 ,2 ]
Li, Qian [1 ,2 ]
Zhang, Lei [3 ]
Guo, Jinhong [4 ]
Xu, Zhigang [1 ,2 ]
Kang, Yuejun [1 ,2 ]
机构
[1] Southwest Univ, Fac Mat & Energy, Inst Clean Energy & Adv Mat, Chongqing 400715, Peoples R China
[2] Chongqing Engn Res Ctr Micronano Biomed Mat & Devi, Chongqing 400715, Peoples R China
[3] Southwest Univ, State Key Lab Silkworm Genome Biol, Chongqing 400716, Peoples R China
[4] Univ Elect Sci & Technol China, Chengdu 611731, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Synergistic therapeutics; Photothermal therapy; Drug release; Magnetic targeting; Biocompatibility; MESOPOROUS SILICA NANOPARTICLES; PRUSSIAN BLUE NANOPARTICLES; DRUG-DELIVERY-SYSTEMS; POLYMERIC NANOPARTICLES; FE3O4; NANOPARTICLES; IN-VITRO; CANCER; THERAPY; DOXORUBICIN; NANOSPHERES;
D O I
10.1016/j.colsurfb.2017.09.012
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The integration of multifunctional therapeutic capabilities into a single nanosystem has attracted much attention for use as an efficient cancer therapy. However, developing biocompatible therapeutic nano agents with desirable safety, efficiency, targeting, and synergistic effects remains challenging. Herein, we designed a class of multifunctional PEGylated magnetic nanoparticles (NPs) with a core-shell structure and polydopamine (PDA) coating, which were loaded with the anticancer drug doxorubicin (DOX) for simultaneous targeted chemotherapy and photothermal ablation of tumour cells. This nanosystem showed strong near-infrared absorption due to the polydopamine layer and was capable of magnetic field-guided drug delivery due to the superparamagnetism of the carrier. The resultant product exhibited excellent stability and biocompatibility in vitro due to the PEGylation of dopamine. Notably, the combination of chemotherapy and photothermal therapy had an evident synergistic effect on the ablation of tumour cells. This multifunctional nanoplatform has promising potential as an efficient therapeutic agent for multimodal cancer treatment. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 21
页数:11
相关论文
共 52 条
[1]  
[Anonymous], SENS BASEL
[2]   Near-infrared light-responsive inorganic nanomaterials for photothermal therapy [J].
Bao, Zhihong ;
Liu, Xuerong ;
Liu, Yangdi ;
Liu, Hongzhuo ;
Zhao, Kun .
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2016, 11 (03) :349-364
[3]   Thermal Tumor Ablation in Clinical Use [J].
Brace, Chris .
IEEE PULSE, 2011, 2 (05) :28-38
[4]   Nanochemistry and Nanomedicine for Nanoparticle-based Diagnostics and Therapy [J].
Chen, Guanying ;
Roy, Indrajit ;
Yang, Chunhui ;
Prasad, Paras N. .
CHEMICAL REVIEWS, 2016, 116 (05) :2826-2885
[5]   Polypyrrole nanoparticles for high-performance in vivo near-infrared photothermal cancer therapy [J].
Chen, Mei ;
Fang, Xiaoliang ;
Tang, Shaoheng ;
Zheng, Nanfeng .
CHEMICAL COMMUNICATIONS, 2012, 48 (71) :8934-8936
[6]   Construction of a high-performance magnetic enzyme nanosystem for rapid tryptic digestion [J].
Cheng, Gong ;
Zheng, Si-Yang .
SCIENTIFIC REPORTS, 2014, 4
[7]   Nanoparticle-based combination drug delivery systems for synergistic cancer treatment [J].
Choi J.Y. ;
Thapa R.K. ;
Yong C.S. ;
Kim J.O. .
Journal of Pharmaceutical Investigation, 2016, 46 (4) :325-339
[8]   Preparation of Fe3O4 magnetic nanoparticles coated with gallic acid for drug delivery [J].
Dorniani, Dena ;
Bin Hussein, Mohd Zobir ;
Kura, Aminu Umar ;
Fakurazi, Sharida ;
Shaari, Abdul Halim ;
Ahmad, Zalinah .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :5745-5756
[9]   Antibody-targeted nanoparticles for cancer therapy [J].
Fay, Francois ;
Scott, Christopher J. .
IMMUNOTHERAPY, 2011, 3 (03) :381-394
[10]   Cancer nanotechnology: Opportunities and challenges [J].
Ferrari, M .
NATURE REVIEWS CANCER, 2005, 5 (03) :161-171