Bimetallic Au–Ag nanocages extended TPP conjugate structure for self-enhancing therapy of tumors
Abstract
Abstract
Mitochondria are particularly sensitive to heat and also can be easily damaged by reactive oxygen species (ROS). However, due to the extremely complicated microenvironment in tumors, monotherapies targeting mitochondria often fail to achieve desired results. To solve this problem, we synthesized Au–Ag cages via electrical substitution reaction and linked mitochondrial-targeting molecular (4-carboxybutyl) triphenyl phosphonium bromide (TPP) to obtain multifunctional nanoplatforms TPP-PEG-Au–Ag cages (TPCs). The self-augmented photothermal therapy (PTT) combined with photodynamic therapy (PDT) achieved triple antitumor treatment. Due to the surface-enhanced Raman scattering between the bimetal and the extended conjugate structure of TPP, the photothermal conversion efficiency of TPCs reached 58.47% under 808 nm laser irradiation, which amounts to an increase of 9.25% compared to the pure Au–Ag cages. Moreover, Ag particles generate more ROS and O
2
through the Fenton reaction to enhance PDT treatment. Cell experiments show that the complementary self-enhancement model of TPCs-Ce6 has excellent anti-cancer effects through PDT/PTT under laser irradiation. Therefore, this work created a multifunctional nanometer agent that realizes a mitochondrial-targeted combination therapy for cancer. It also provides a new idea for improving the light-to-heat conversion efficiency of materials.
Graphic abstract
Keywords
- Mitochondrial targeted,
- Surface-enhanced Raman scattering,
- Photothermal conversion efficiency,
- Fenton reaction,
- Self-enhancement therapy
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