Theranostic
nanoplatforms that integrate therapy and diagnosis in a single composite
have become increasingly attractive in the field of precise and efficient
tumor treatment. Herein, a novel oxygen-deficient zirconia (ZrO2–x) nanosystem based on the conjugation
of thiol-polyethylene glycol-amine (SH-PEG-NH2) and chlorin
e6 (Ce6) was elaborately designed and established for efficacious
photothermal/photodynamic therapy (PTT/PDT) and fluorescence/photoacoustic
(FL/PA) bimodal imaging for the first time. The crystalline-disordered,
PEGylated ZrO2–x nanoparticles
(ZP NPs) displayed strong optical absorption in the near-infrared
(NIR) window and were featured with significant photothermal conversion
capacity. The ZP NPs were further covalently conjugated with Ce6 to
form ZrO2–x@PEG/Ce6 (ZPC) NPs,
which displayed a long circulatory half-life, efficient tumor accumulation,
and outstanding FL/PA imaging performance. Moreover, the nanocomposites
effectively generated cytotoxic intracellular reactive oxygen species
(ROS) responsive to laser activation. Both cell studies and animal
experiments explicitly demonstrated that ZPC NPs mediated remarkable
tumor ablation with minimal systemic toxicity thanks to their tumor-specific
PTT/PDT effect. Collectively, these findings may open up new avenues
to broaden the application of oxygen-deficient ZrO2–x nanostructures as high-performance photothermal
agents in tumor theranostics through rational design and accurate
control of their physiochemical properties.