Liposarcoma is one of the most common soft tissue sarcomas.
It
grows rapidly and is difficult to diagnose, until complications occur.
Clinical surgery has become the only treatment strategy without any
specific medicine available. The propensity for relapse urgently calls
for the development of improved technologies. Nanotechnology-based
technologies allow the early and accurate diagnosis and multifunctional
treatment of liposarcoma, which has broad application prospects in
clinical precision therapy. In this study, we describe a novel therapeutic
strategy based on the near-infrared-mediated self-assembly of nanoprobes
to effectively combat liposarcoma. We synthesized a novel type of
graphene quantum dot (GQD), self-assembled with gadolinium ion (Gd3+) and IR820 dye by electrostatic adsorption, and then bonded
the heat shock protein inhibitor 17-allylamino-17-demethoxy-geldanamycin
(17-AAG) via electrostatic incorporation, resulting in innovative
multifunctional IR820-triggerable GQD-Gd/IR820@AAG nanoprobes. This
self-assembly system has been shown to be highly effective for in
vivo and in vitro delivery and can be easily excreted after dissociation
in vivo with greatly reduced biotoxicity. In vivo experiments demonstrated
that the GQD-Gd/IR820@AAG nanoprobes induced downregulated heat shock
protein expression in tumor cells, thereby reducing their heat tolerance
threshold and effectively enhancing the effect of mild photothermal
therapy. In addition, the nanoprobes displayed outstanding T
1-magnetic resonance and near-infrared fluorescence
imaging, owing to the presence of Gd3+ and IR820, respectively.
The designed nanoprobes have considerable potential therapeutic value
against liposarcomas.