4.8 Article

Cancer Cell Detection and Therapeutics Using Peroxidase-Active Nanohybrid of Gold Nanoparticle-Loaded Mesoporous Silica-Coated Graphene

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 7, Issue 18, Pages 9807-9816

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b01758

Keywords

cancer cell detection; gold nanoparticles; graphene; peroxidase activity; therapeutics

Funding

  1. National Research Foundation (NRF), Prime Minister's Office, Singapore under its NRF Fellowship [NRF2009NRF-RF001-015]
  2. Campus for Research Excellence and Technological Enterprise (CREATE) Programme, Singapore Peking University Research Centre for a Sustainable Low-Carbon Future
  3. NTU-A*STAR Silicon Technologies Centre of Excellence [1123510003]
  4. NTU-Northwestern Institute for Nanomedicine

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Development of efficient artificial enzymes is an emerging field in nanobiotechnology, since these artificial enzymes could overcome serious disadvantages of natural enzymes. In this work, a new nanostructured hybrid was developed as a mimetic enzyme for in vitro detection and therapeutic treatment of cancer cells. The hybrid (GSF@AuNPs) was prepared by the immobilization of gold nanoparticles (AuNPs) on mesoporous silica-coated nanosized reduced graphene oxide conjugated with folic acid, a cancer cell-targeting ligand. The GSF@AuNPs hybrid showed unprecedented peroxidase-like activity, monitored by catalytic oxidation of a typical peroxidase substrate, 3,3',5,5'-tetramethylbenzidine (TMB), in the presence of H2O2. On basis of this peroxidase activity, the hybrid was utilized as a selective, quantitative, and fast colorimetric detection probe for cancer cells. Finally, the hybrid as a mimetic enzyme was employed for H2O2- and ascorbic acid (AA)-mediated therapeutics of cancer cells. In vitro experiments using human cervical cancer cells (HeLa cells) exhibited the formation of reactive oxygen species (OH center dot radical) in the presence of peroxidase-mimic GSF@AuNPs with either exogenous H(2)O2 or endogenous H2O2 generated from AA, leading to an enhanced cytotoxicity to HeLa cells. In the case of normal cells (human embryonic kidney HEK 293 cells), the treatment with the hybrid and H2O2 or AA showed no obvious damage, proving selective killing effect of the hybrid to cancer cells.

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