Carboxymethyl cellulose modified graphene oxide as pH-sensitive drug delivery system

被引:119
作者
Rao, Ziqie [1 ]
Ge, Hongyu [1 ]
Liu, Liangling [1 ]
Zhu, Chen [1 ]
Min, Lian [1 ]
Liu, Meng [1 ]
Fan, Lihong [1 ]
Li, Dan [1 ]
机构
[1] Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Hubei, Peoples R China
关键词
Graphene oxide; Carboxymethyl cellulose; Doxorubicin hydrochloride; Drug delivery; Controlled release; MECHANICAL-PROPERTIES; CONTROLLED-RELEASE; ANTITUMOR DRUG; CANCER-THERAPY; COMPOSITES; CHITOSAN; BIOCOMPATIBILITY; NANOSHEETS; DOCETAXEL; CARRIER;
D O I
10.1016/j.ijbiomac.2017.09.096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanotechnology has been studied to improve drug delivery and cancer treatment. The aim of this study is to introduce amino groups into graphene oxide (GO) to form aminated fumed graphene (GO-ADH) and combine GO-ADH with carboxymethyl cellulose (CMC) to produce GO-CMC complex as a drug carrier matrix. The anti-cancer drug small molecule doxorubicin hydrochloride (DOX) was bond to GO-CMC by pi-pi bond interaction and hydrogen bonding to form GO-CMC/DOX drug loading system. Via the FT-IR, transmission electron microscopy (TEM) and Zeta potential analyzer analysis showed that GO-CMC complex was successfully synthesized. Studies have shown that when pH = 5.0, the cumulative release rate of drugs can reach 65.2%, which means it has pH-sensitive ability. The cells were treated with MTT method and human cervical cancer cells (Hela cells) and mouse fibroblasts (NIH-3T3 cells). The results showed that GO-CMC had no obvious cytotoxicity and good biocompatibility. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1184 / 1192
页数:9
相关论文
共 44 条
  • [1] Asghar A., 2014, INT J FOOD ENG, V29, P237
  • [2] Preparation and characterization of double crosslinked hydrogel films from carboxymethylchitosan and carboxymethylcellulose
    Bao, Dengshan
    Chen, Mingjie
    Wang, Haiying
    Wang, Jufang
    Liu, Chuanfu
    Sun, Runcang
    [J]. CARBOHYDRATE POLYMERS, 2014, 110 : 113 - 120
  • [3] Chitosan-Functionalized Graphene Oxide as a Nanocarrier for Drug and Gene Delivery
    Bao, Hongqian
    Pan, Yongzheng
    Ping, Yuan
    Sahoo, Nanda Gopal
    Wu, Tongfei
    Li, Lin
    Li, Jun
    Gan, Leong Huat
    [J]. SMALL, 2011, 7 (11) : 1569 - 1578
  • [4] Distribution and clearance of PEG-single-walled carbon nanotube cancer drug delivery vehicles in mice
    Bhirde, Ashwin A.
    Patel, Sachin
    Sousa, Alioscka A.
    Patel, Vyomesh
    Molinolo, Alfredo A.
    Ji, Youngmi
    Leapman, Richard D.
    Gutkind, J. Silvio
    Rusling, James F.
    [J]. NANOMEDICINE, 2010, 5 (10) : 1535 - 1546
  • [5] Polyethylenimine-functionalized graphene oxide as an efficient gene delivery vector
    Chen, Biao
    Liu, Min
    Zhang, Liming
    Huang, Jie
    Yao, Jianlin
    Zhang, Zhijun
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (21) : 7736 - 7741
  • [6] Biomedical Applications of Graphene and Graphene Oxide
    Chung, Chul
    Kim, Young-Kwan
    Shin, Dolly
    Ryoo, Soo-Ryoon
    Hong, Byung Hee
    Min, Dal-Hee
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2013, 46 (10) : 2211 - 2224
  • [7] Fabrication, Mechanical Properties, and Biocompatibility of Graphene-Reinforced Chitosan Composites
    Fan, Hailong
    Wang, Lili
    Zhao, Keke
    Li, Nan
    Shi, Zujin
    Ge, Zigang
    Jin, Zhaoxia
    [J]. BIOMACROMOLECULES, 2010, 11 (09) : 2345 - 2351
  • [8] THE INFLUENCE OF POLYMERIC EXCIPIENTS ON DRUG RELEASE FROM HYDROXYPROPYLMETHYLCELLULOSE MATRICES
    FEELY, LC
    DAVIS, SS
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1988, 44 (1-3) : 131 - 139
  • [9] IMPORTANCE OF DRUG TYPE, TABLET SHAPE AND ADDED DILUENTS ON DRUG RELEASE KINETICS FROM HYDROXYPROPYLMETHYLCELLULOSE MATRIX TABLETS
    FORD, JL
    RUBINSTEIN, MH
    MCCAUL, F
    HOGAN, JE
    EDGAR, PJ
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 40 (03) : 223 - 234
  • [10] Functionalized graphene oxide modified polysebacic anhydride as drug carrier for levofloxacin controlled release
    Gao, Jie
    Bao, Feng
    Feng, Lingling
    Shen, Kaiyan
    Zhu, Qiandong
    Wang, Dongfang
    Chen, Tao
    Ma, Rui
    Yan, Chunjie
    [J]. RSC ADVANCES, 2011, 1 (09) : 1737 - 1744