Poly(acrylic acid) conjugated hollow mesoporous carbon as a dual-stimuli triggered drug delivery system for chemo-photothermal synergistic therapy

被引:28
|
作者
Li, Xian [1 ]
Liu, Chang [1 ]
Wang, Shengyu [1 ]
Jiao, Jian [1 ]
Di, Donghua [1 ]
Jiang, Tongying [1 ]
Zhao, Qinfu [1 ]
Wang, Siling [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, 103 Wenhua Rd, Shenyang 110016, Liaoning Provin, Peoples R China
基金
中国国家自然科学基金;
关键词
Hollow mesoporous carbon; Disulfide bonds; Dual stimuli-responsive; Photothermal therapy; Poly(acrylic acid); Doxorubicin; SILICA NANOPARTICLES; CANCER-THERAPY; NANOTUBES; RELEASE; LIGHT; IRRADIATION; PLATFORM; CELLS;
D O I
10.1016/j.msec.2016.10.037
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 work, we described the development of the redox and pH dual stimuli-responsive drug delivery system and combination of the chemotherapy and photothermal therapy for cancer treatment. The poly(acrylic acid) (PAA) was conjugated on the outlets of hollow mesoporous carbon (HMC) via disulfide bonds. PM was used as a capping to block drug within the mesopores of HMC for its lots of favorable advantages, such as good biocom-patibility, appropriate molecular weight to block the mesopores of HMC, extension of the blood circulation, and the improvement of the dispersity of the nano-carriers in physiological environment. The DOX loaded DOX/ HMC-SS-PAA had a high drug loading amount up to 51.9%. The in vitro drug release results illustrated that DOX/HMC-SS-PM showed redox and pH dual-responive drug release, and the release rate could be further improved by the near infrared (NIR) irradiation. Cell viability experiment indicated that DOX/HMC-SS-PM had a synergistic therapeutic effect by combination of chemotherapy and photothermal therapy. This work suggested that HMC-SS-PM exhibited dual-responsive drug release "property and could be used as a NIR-adsorbing drug delivery system for chemo-photothermal synergistic therapy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:594 / 603
页数:10
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