• 文献标题:   Multifunctional graphene-based magnetic nanocarriers for combined hyperthermia and dual stimuli-responsive drug delivery
  • 文献类型:   Article
  • 作  者:   RODRIGUES RO, BALDI G, DOUMETT S, GARCIAHEVIA L, GALLO J, BANOBRELOPEZ M, DRAZIC G, CALHELHA RC, FERREIRA ICFR, LIMA R, GOMES HT, SILVA AMT
  • 作者关键词:   graphene magnetic nanoparticle, magnetic hyperthermia, controlleddrug release, cancer therapy, doxorubicin
  • 出版物名称:   MATERIALS SCIENCE ENGINEERING CMATERIALS FOR BIOLOGICAL APPLICATIONS
  • ISSN:   0928-4931 EI 1873-0191
  • 通讯作者地址:   Polytech Inst Braganca
  • 被引频次:   8
  • DOI:   10.1016/j.msec.2018.07.060
  • 出版年:   2018

▎ 摘  要

The synthesis of hydrophilic graphene-based yolk-shell magnetic nanoparticles functionalized with copolymer pluronic F-127 (GYSMNP@PF127) is herein reported to achieve an efficient multifunctional biomedical system for mild hyperthermia and stimuli-responsive drug delivery. In vitro tests revealed the extraordinary ability of GYSMNP@PF127 to act as smart stimuli-responsive multifunctional nanomedicine platform for cancer therapy, exhibiting (i) an outstanding loading capacity of 91% (w/w, representing 910 mu g mg(-1)) of the chemotherapeutic drug doxorubicin, (ii) a high heating efficiency under an alternating (AC) magnetic field (intrinsic power loss ranging from 2.1-2.7 nHm(2) kg(-1)), and (iii) a dual pH and thermal stimuli-responsive drug controlled release (46% at acidic tumour pH vs 7% at physiological pH) under AC magnetic field, in just 30 (nth. Additionally, GYSMNP@PF127 presents optimal hydrodynamic diameter (D-H = 180 mn) with negative surface charge, high haemocompatibility for blood stream applications and tumour cellular uptake of drug nanocarriers. Due to its physicochemical, magnetic and biocompatibility properties, the developed graphene-based magnetic nano carrier shows high promise as dual exogenous (AC field)/endogenous (pH) stimuli-responsive actuators for targeted thermo-chemotherapy, combining magnetic hyperthermia and controlled drug release triggered by the abnormal tumour environment. The presented strategy and findings can represent a new way to design and develop highly stable added-value graphene-based nanostructures for the combined treatment of cancer.