A nanoplatform based on mesoporous silica-coated gold nanorods for cancer triplex therapy

J Mater Chem B. 2020 Nov 4;8(42):9686-9696. doi: 10.1039/d0tb01707h.

Abstract

To enhance the efficacy of nanoparticle-based cancer therapy with reduced side effects and promote its clinical translation, a biocompatible nanocomposite based on mesoporous silica-coated gold nanorods (AuNR@MSN) for triple tumor therapy is reported in this study. The gold core served as a hyperthermia agent, while the MSN shell acted as a reservoir of chemotherapeutics owing to its excellent loading capacity. Cytochrome c with the apoptosis inducing function was anchored on the surface of AuNR@MSN to prevent drug leakage through redox-responsive disulfide bonds. The successful construction of a nanocomposite was confirmed by characterization of the physicochemical properties. In vitro and in vivo studies demonstrated that the nanocomposite displayed an optimizing anti-tumor effect with a synergistic strategy of excellent photothermal therapy, chemotherapy and protein therapy. Therefore, this cooperative strategy paves the way for high-efficiency oncotherapy with reduced side effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy*
  • Cytochromes c / chemistry
  • Cytochromes c / therapeutic use*
  • Delayed-Action Preparations / chemistry
  • Drug Delivery Systems
  • Female
  • Gold / chemistry
  • Gold / therapeutic use*
  • Humans
  • Hyperthermia, Induced
  • MCF-7 Cells
  • Mice, Nude
  • Nanotubes* / chemistry
  • Nanotubes* / ultrastructure
  • Oxidation-Reduction
  • Porosity
  • Silicon Dioxide / chemistry
  • Silicon Dioxide / therapeutic use*

Substances

  • Delayed-Action Preparations
  • Gold
  • Silicon Dioxide
  • Cytochromes c