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
相关论文
共 48 条
  • [11] Gold nanoparticle-conjugated heterogeneous polymer brush-wrapped cellulose nanocrystals prepared by combining different controllable polymerization techniques for theranostic applications
    Hu, Hao
    Hou, Xiu-Ju
    Wang, Xiao-Chen
    Nie, Jing-Jun
    Cai, Qing
    Xu, Fu-Jian
    [J]. POLYMER CHEMISTRY, 2016, 7 (18) : 3107 - 3116
  • [12] Facile synthesis of hyaluronic acid-modified Fe3O4/Au composite nanoparticles for targeted dual mode MR/CT imaging of tumors
    Hu, Yong
    Yang, Jia
    Wei, Ping
    Li, Jingchao
    Ding, Ling
    Zhang, Guixiang
    Shi, Xiangyang
    Shen, Mingwu
    [J]. JOURNAL OF MATERIALS CHEMISTRY B, 2015, 3 (47) : 9098 - 9108
  • [13] Facile synthesis of RGD peptide-modified iron oxide nanoparticles with ultrahigh relaxivity for targeted MR imaging of tumors
    Hu, Yong
    Li, Jingchao
    Yang, Jia
    Wei, Ping
    Luo, Yu
    Ding, Ling
    Sun, Wenjie
    Zhang, Guixiang
    Shi, Xiangyang
    Shen, Mingwu
    [J]. BIOMATERIALS SCIENCE, 2015, 3 (05) : 721 - 732
  • [14] Biomedical nanomaterials for imaging-guided cancer therapy
    Huang, Yuran
    He, Sha
    Cao, Weipeng
    Cai, Kaiyong
    Liang, Xing-Jie
    [J]. NANOSCALE, 2012, 4 (20) : 6135 - 6149
  • [15] Effective delivery of immunosuppressive drug molecules by silica coated iron oxide nanoparticles
    Hwang, Jangsun
    Lee, Eunwon
    Kim, Jieun
    Seo, Youngmin
    Lee, Kwan Hong
    Hong, Jong Wook
    Gilad, Assaf A.
    Park, Hansoo
    Choi, Jonghoon
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 2016, 142 : 290 - 296
  • [16] Nanostructured SERS-electrochemical biosensors for testing of anticancer drug interactions with DNA
    Ilkhani, Hoda
    Hughes, Taylor
    Li, Jing
    Zhong, Chuan Jian
    Hepel, Maria
    [J]. BIOSENSORS & BIOELECTRONICS, 2016, 80 : 257 - 264
  • [17] Thailandepsin A-loaded and octreotide-functionalized unimolecular micelles for targeted neuroendocrine cancer therapy
    Jaskula-Sztul, Renata
    Xu, Wenjin
    Chen, Guojun
    Harrison, April
    Dammalapati, Ajitha
    Nair, Renu
    Cheng, Yiqiang
    Gong, Shaoqin
    Chen, Herbert
    [J]. BIOMATERIALS, 2016, 91 : 1 - 10
  • [18] Ultrasound-enhanced chemiluminescence tomography in biological tissue
    Kobayashi, Masaki
    Kikuchi, Naoto
    Sato, Akihiro
    [J]. ULTRASONICS SONOCHEMISTRY, 2016, 31 : 1 - 6
  • [19] In Vivo Targeted Delivery of Nanoparticles for Theranosis
    Koo, Heebeom
    Huh, Myung Sook
    Sun, In-Cheol
    Yuk, Soon Hong
    Choi, Kuiwon
    Kim, Kwangmeyung
    Kwon, Ick Chan
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2011, 44 (10) : 1018 - 1028
  • [20] Salicylic Acid Conjugated Dendrimers Are a Tunable, High Performance CEST MRI NanoPlatform
    Lesniak, Wojciech G.
    Oskolkov, Nikita
    Song, Xiaolei
    Lal, Bachchu
    Yang, Xing
    Pornper, Martin
    Laterra, John
    Nimmagadda, Sridhar
    McMahon, Michael T.
    [J]. NANO LETTERS, 2016, 16 (04) : 2248 - 2253