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Time-of-flight secondary ion mass spectrometry (TOF-SIMS) was used for an in situ thermal decomposition study of Zn(CH 3 COO) 2 ·2H 2 O forming ZnO nanoparticles. TOF-SIMS spectra were recorded at regular temperature intervals of 25• C in positive and negative detection modes in a dynamic thermal process.Controlled heating (5 • C min −1 ) of Zn(CH 3 COO) 2 ·2H 2 O was also carried out using thermogravimetric analysis (TGA) in an oxygen atmosphere (20 ml min −1 ). Nearly spherical ZnO nanoparticles with no agglomeration and a narrow size distribution (diameter ∼50 nm) were observed, which were characterized using scanning electron microscopy, transmission electron microscopy and x-ray diffraction. In situ thermo-TOF-SIMS was used to monitor the 64 Zn + and 66 Zn + ion abundances as a function of temperature, which showed a similar profile to that observed for weight loss in TGA during decomposition. Based on the experimental results, a possible decomposition mechanism for the formation of ZnO is proposed.

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In this study, for the first time, CuFeS nanocrystals were successfully prepared through a facile noninjection-based synthetic strategy, by reacting Cu and Fe precursors with dodecanethiol in a 1-octadecene solvent. This one-pot noninjection strategy features easy handling, large-scale production, and high synthetic reproducibility. Following hyaluronic acid (HA) encapsulation, CuFeS nanocrystals coated with HA (CuFeS@HA) not only readily dispersed in water and showed improved biocompatibility but also possessed a tumor-specific targeting ability of cancer cells bearing the cluster determinant 44 (CD44) receptors. The encapsulated CuFeS@HA showed broad optical absorbance from the visible to the near-infrared (NIR) region and high photothermal conversion efficiencies of about 74.2%. They can, therefore, be utilized for the photothermal ablation of cancer cells with NIR light irradiation. In addition, toxicity studies in vitro (B16F1 and HeLa) and in vivo (zebrafish embryos), as well as in vitro blood compatibility studies, indicated that CuFeS@HA show low cytotoxicity at the doses required for photothermal therapy. More importantly, CuFeS@HA can be used as delivery vehicles for chemotherapy cisplatin(IV) prodrug forming CuFeS@HA-Pt(IV). Their release profile revealed pH- and glutathione-mediated drug release from CuFeS@HA-Pt(IV), which may minimize the side effects of the drug to normal tissues during therapy. Subsequent in vitro experiments confirmed that the use of CuFeS@HA-Pt(IV) provides an enhanced and synergistic therapeutic effect compared to that from the use of either chemotherapy or photothermal therapy alone.