Rattle-type Au@Cu2-xS hollow mesoporous nanocrystals with enhanced photothermal efficiency for intracellular oncogenic microRNA detection and chemo-photothermal therapy

Biomaterials. 2018 Mar:158:23-33. doi: 10.1016/j.biomaterials.2017.12.009. Epub 2017 Dec 13.

Abstract

The coupling of the localized surface plasma resonance (LSPR) between noble metals of Au, Ag and Cu and semiconductors of Cu2-xE (E = S, Se, Te) opens new regime to design photothermal (PT) agents with enhanced PT conversion efficiency. However, it is rarely explored on fabricating of engineered dual plasmonic hybrid nanosystem for combinatory therapeutic-diagnostic applications. Herein, rattle-type Au@Cu2-xS hollow mesoporous nanoparitcles with advanced PT conversion efficiency are designed for cellular vehicles and chemo-photothermal synergistic therapy platform. The LSPR coupling between the Au core and Cu2-xS shell are investigated experimentally and theoretically to generate a PT conversion efficiency high to 35.2% and enhanced by 11.3% than that of Cu2-xS. By conjugating microRNA (miRNA) gene probe on the surface, it can realize the intracellular oncogenic miRNA detection. After loading of anticancer drug doxorubicin into the cavity of the Au@Cu2-xS, the antitumor therapy efficacy is greatly enhanced in vitro and in vivo due to the NIR photoactivation chemo- and photothermal synergistic therapy. The rattle-type metal-semiconductor hollow mesoporous nanostructure with efficient LSPR coupling and high cargo loading capability will be beneficial to future design of LSPR-based photothermal agents for a broad range of biomedical application.

Keywords: Chemo-photothermal therapy; Localized surface plasma resonance coupling; MicroRNA detection; Rattle-type Au@Cu(2−x)S; Theranostic platform.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Combined Modality Therapy
  • Doxorubicin / pharmacology
  • Drug Carriers* / chemistry
  • Humans
  • MCF-7 Cells
  • MicroRNAs* / analysis
  • Nanoparticles* / chemistry
  • Neoplasms / genetics
  • Neoplasms / therapy
  • Phototherapy* / methods
  • Surface Plasmon Resonance
  • Theranostic Nanomedicine

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • MicroRNAs
  • Doxorubicin