No abstract

The efficient and specific delivery of nanoparticles (NPs) to brain tumors is crucial for successful glioma treatment. Heparin‐based polymers decorated with two peptides self‐assemble into multi‐functional NPs that specifically target glioma cells. These NPs re‐self‐assemble to a smaller size in blood, which is beneficial for in‐vivo brain drug delivery. The hydrodynamic size of one type of these NPs is 63 ± 11 nm under blood‐mimic conditions (10% fetal bovine serum), but it is 164 ± 16 nm in water. Additionally their zeta potential is more neutral in the blood‐mimic conditions. Transmission electron microscopy reveals the morphology of the spherical NPs. In vitro experiments demonstrate that the NPs exhibit a high cellular uptake and the ability to efficiently discourage proliferation, endothelial‐lined vessels, and vasculogenic mimicry. In vivo studies demonstrate that the NPs can by‐pass the normal blood–brain and blood–(brain tumor) barriers and specifically accumulate in glioma tissues; moreover, they present an excellent anti‐glioma effect in subcutaneous/intracranial glioma‐bearing mice. Their superiority is due to their appropriate size in blood and the synergic effect arising from their targeting of two different receptors. The data suggests that these NPs are ideal for anti‐glioma therapy.

Developing a facile and reliable method for the fabrication of transition metal chalcogenides is a vital and endless pursuit of scientific and technological disciplines. In this work, we develop a one-pot solution approach to obtain copper selenide nanostructures with different morphologies and crystal structures (CuSe nanoparticles, CuSe nanoplates and CuSe nanosheets). In comparison to previously reported methods, our method did not use expensive and very toxic raw materials. After detailed studies of reaction conditions, including temperature, reaction time, and feeding amount of surfactants and precursors, we found that the feeding ratio of precursors played a key role in the crystal structures and morphologies of the final products. Moreover, as a proof-of-concept study, the potential applications of the as-prepared copper selenide nanostructures in the photocatalytic discoloration of aqueous methylene blue (MB) under visible light irradiation and near-infrared (NIR) light induced photothermal therapy for cancer treatment were investigated. Encouraged by their strong photocatalytic activities and high photothermal conversion efficiencies (calculated to be 51.0%, 49.5% and 48.9% for CuSe nanoparticles, CuSe nanoplates and CuSe nanosheets, respectively), we believe that copper selenide nanostructures fabricated from the one-pot solution approach developed in this work would be promising candidates for a wide variety of emerging applications.

PEGylated rhenium nanoclusters were developed as a degradable and renal-clearable metallic photothermal nanoagent for CT imaging and tumor therapy.