Folic acid-functionalized graphene oxide nanosheets via plasma etching as a platform to combine NIR anticancer phototherapy and targeted drug delivery

被引:65
作者
Mauro, Nicold [1 ,2 ]
Scialabba, Cinzia [1 ]
Agnello, Simonpietro [3 ]
Cavallaro, Gennara [1 ]
Giammona, Gaetano [1 ,4 ]
机构
[1] Univ Palermo, Dept Sci & Tecnol Biol Chim & Farmaceut STEBICEF, Lab Biocompatible Polymers, Via Archirafi 32, I-90123 Palermo, Italy
[2] Fdn Umberto Veronesi, Piazza Velasca 5, I-20122 Milan, Italy
[3] Univ Palermo, Dept Fis & Chim Emilio Segre, Via Archirafi 36, I-90123 Palermo, Italy
[4] Italian Natl Res Council, Inst Biophys, Via Ugo La Malfa 153, I-90146 Palermo, Italy
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2020年 / 107卷
关键词
Graphene oxide; Breast cancer; Doxorubicin; Folic acid; Phototherapy; CANCER-CELLS; DOXORUBICIN; NANOPARTICLES; NANOMEDICINE; ABLATION; SYSTEM; AGENTS;
D O I
10.1016/j.msec.2019.110201
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
PEGylated graphene oxide (GO) has shown potential as NIR converting agent to produce local heat useful in breast cancer therapy, since its suitable photothermal conversion, high stability in physiological fluids, biocompatibility and huge specific surface. GO is an appealing nanomaterial for potential clinical applications combining drug delivery and photothermal therapy in a single nano-device capable of specifically targeting breast cancer cells. However, native GO sheets have large dimensions (0.5-5 mu m) such that tumor accumulation after a systemic administration is usually precluded. Herein, we report a step-by-step synthesis of folic acid-functionalized PEGylated GO, henceforth named GO-PEG-Fol, with small size and narrow size distribution (similar to 30 +/- 5 nm), and the ability of efficiently converting NIR light into heat. GO-PEG-Fol consists of a nano-GO sheet, obtained by fragmentation of GO by means of non-equilibrium plasma etching, fully functionalized with folic acid-terminated PEG(2000) chains through amidic coupling and azide-alkyne click cycloaddition, which we showed as active targeting agents to selectively recognize breast cancer cells such as MCF7 and MDA-MB-231. The GO-PEG-Fol incorporated a high amount of doxorubicin hydrochloride (Doxo) (> 33%) and behaves as NIR-light-activated heater capable of triggering sudden Doxo delivery inside cancer cells and localized hyperthermia, thus provoking efficient breast cancer death. The cytotoxic effect was found to be selective for breast cancer cells, being the IC50 up to 12 times lower than that observed for healthy fibroblasts. This work established plasma etching as a cost-effective strategy to get functionalized nano-GO with a smart combination of properties such as small size, good photothermal efficiency and targeted cytotoxic effect, which make it a promising candidate as photothermal agent for the treatment of breast cancer.
引用
收藏
页数:14
相关论文
共 53 条
  • [1] A new chemotherapy agent-free theranostic system composed of graphene oxide nano-complex and aptamers for treatment of cancer cells
    Bahreyni, Amirhossein
    Yazdian-Robati, Rezvan
    Hashemitabar, Shirin
    Ramezani, Mohammad
    Ramezani, Pouria
    Abnous, Khalil
    Taghdisi, Seyed Mohammad
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 526 (1-2) : 391 - 399
  • [2] In vivo theranostics with near-infrared-emitting carbon dots-highly efficient photothermal therapy based on passive targeting after intravenous administration
    Bao, Xin
    Yuan, Ye
    Chen, Jingqin
    Zhang, Bohan
    Li, Di
    Zhou, Ding
    Jing, Pengtao
    Xu, Guiying
    Wang, Yingli
    Hola, Katerina
    Shen, Dezhen
    Wu, Changfeng
    Song, Liang
    Liu, Chengbo
    Zboril, Radek
    Qu, Songnan
    [J]. LIGHT-SCIENCE & APPLICATIONS, 2018, 7
  • [3] Bhatia S.N., 2009, CANC RES
  • [4] Graphene Oxide Triggers Toll-Like Receptors/Autophagy Responses In Vitro and Inhibits Tumor Growth In Vivo
    Chen, Guan-Yu
    Chen, Chiu-Ling
    Tuan, Hsing-Yu
    Yuan, Pei-Xiang
    Li, Kuei-Chang
    Yang, Hong-Jie
    Hu, Yu-Chen
    [J]. ADVANCED HEALTHCARE MATERIALS, 2014, 3 (09) : 1486 - 1495
  • [5] Reducible polyamidoamine-magnetic iron oxide self-assembled nanoparticles for doxorubicin delivery
    Chen, Jun
    Shi, Min
    Liu, Pengmin
    Ko, Alex
    Zhong, Wen
    Liao, WangJun
    Xing, Malcolm M. Q.
    [J]. BIOMATERIALS, 2014, 35 (04) : 1240 - 1248
  • [6] Graphene Oxide-Gallic Acid Nanodelivery System for Cancer Therapy
    Dorniani, Dena
    Saifullah, Bullo
    Barahuie, Farahnaz
    Arulselvan, Palanisamy
    Bin Hussein, Mohd Zobir
    Fakurazi, Sharida
    Twyman, Lance J.
    [J]. NANOSCALE RESEARCH LETTERS, 2016, 11
  • [7] Controlled functionalization of graphene oxide with sodium azide
    Eigler, Siegfried
    Hu, Yichen
    Ishii, Yoshitaka
    Hirsch, Andreas
    [J]. NANOSCALE, 2013, 5 (24) : 12136 - 12139
  • [8] Application of Evolutionary Principles to Cancer Therapy
    Enriquez-Navas, Pedro M.
    Wojtkowiak, Jonathan W.
    Gatenby, Robert A.
    [J]. CANCER RESEARCH, 2015, 75 (22) : 4675 - 4680
  • [9] Hetero-Difunctional Dimers as Building Blocks for the Synthesis of Poly(amidoamine)s With Hetero-Difunctional Chain Terminals and Their Derivatives
    Ferruti, Paolo
    Mauro, Nicolo
    Manfredi, Amedea
    Ranucci, Elisabetta
    [J]. JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (23) : 4947 - 4957
  • [10] Double-Network-Structured Graphene Oxide-Containing Nanogels as Photothermal Agents for the Treatment of Colorectal Cancer
    Fiorica, Calogero
    Mauro, Nicolo
    Pitarresi, Giovanna
    Scialabba, Cinzia
    Palumbo, Fabio S.
    Giammona, Gaetano
    [J]. BIOMACROMOLECULES, 2017, 18 (03) : 1010 - 1018