We reported an aqueous synthesis of urchin-like gold nanoparticles (NPs) in the presence of hydroquinone through a seed-mediated growth approach. By altering the feed ratio of hydroquinone, seeds, and additional HAuCl4, the diameters of urchin-like NPs were tunable from 55 to 200 nm. Accordingly, the centers of surface plasmon resonance absorption shifted from 555 to 702 nm. Systematical analysis revealed that the generation of urchin-like particles as well as their size evolution strongly depended on the reactivity of gold ions, mainly controlled by the concentration of hydroquinone. At low hydroquinone concentration, only spherical particles were achieved. The increase of the hydroquinone concentration promoted a kinetics-favored deposition of gold atoms on the (111) lattice planes and thereby the growth of branches. Moreover, the as-prepared urchin-like particles possessed good structural stability, which could be kept in the growth solution for more than 10 days without morphology variation.
Cancer multimodal treatment by combining the effects of different theranostics agents can efficiently improve treatment efficacy and reduce side effects. In this work, we demonstrate the theranostics nanodevices on the basis of Cu-loaded polydopamine nanoparticles (CuPDA NPs), which are able to offer magnetic resonance imaging (MRI)-guided thermochemotherapy (TCT). Systematical studies reveal that after Cu ions loading, the molar extinction coefficient of PDA NPs is greatly enhanced by 4 times, thus improving the performance in photothermal therapy. Despite Cu ions being toxic, the release of Cu is mainly stimulated in acidic environment. Once the NPs deposit in the slightly acidic tumor microenvironment (pH ≈ 6.5-6.8), the release rate boosts ∼30%, which effectively avoids the systematic toxicity during chemotherapy. Meanwhile, due to the increment of the electron-proton dipole-dipole interaction correlation time τ, the spin-lattice relaxation time (T) for PDA NPs is found to be shortened by Cu loading, which boosts the longitudinal relaxivity (r). Hence, CuPDA NPs can be used as T-weighted contrast agent in MRI. In addition, due to the naturally existing DA in the human body with stealth effect, CuPDA NPs have an outstanding tumor retention rate as high as 8.2% ID/g. Further in vitro and in vivo tests indicate that CuPDA NPs possess long blood circulation time, good photothermal and physiological stability, and biocompatibility, which are potential nanodevices for MRI-guided TCT with minimal side effects.
Aqueous Au nanoparticles (NPs) are employed as the building blocks to construct chainlike self-assembly architectures, which greatly enhance the photothermal performance at 808 nm. Biocompatible polypyrrole (PPy) is further adopted as the package material to coat Au NP chains, producing stable photothermal agents. As a result of contributions from chainlike Au, the PPy shell, as well as the Au-PPy composite structures, the capability of photothermal transduction at 808 nm is greatly enhanced, represented by the high photothermal transduction efficiency up to 70%. Primary animal experiment proves that the current composite photothermal agents are efficient in inhibiting tumor growth under an 808 nm irradiation, showing the potentials for in vivo photothermal therapy.
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