Highly conductive pristine graphene electrodes were fabricated by inkjet printing using ethyl cellulose-stabilized ink prepared from pristine graphene. Pristine graphene was generated by exfoliation from graphite using ultrasound-assisted supercritical CO₂. The ink, at concentrations up to 1 mg/mL, was stable for more than 9 months and had compatible fluidic characteristics for efficient and reliable inkjet printing. The inkjet printing patterns of the graphene on diverse substrates were uniform and continuous. After 30 printing passes and annealing at 300 °C for 30 min, the printed films developed a high conductivity of 9.24 × 10³ S/m. The resistivity of the printed electrodes on the flexible substrates increased by less than 5% after 1000 bending cycles and by 5.3% under a folding angle of 180°. The presented exfoliated pristine graphene and the corresponding efficient methods for formulating the ink and fabricating conductive electrodes are expected to have high potential in applications involving graphene-based flexible electronic devices.

In this paper, we demonstrated a simple and cost-effective method to produce graphene from graphite in ethanol using ultrasound assisted with curcumin. The influence of curcumin concentration, starting graphite amount, sonication power, and sonication time on the graphene concentration was studied schematically. The π-π interaction between curcumin and graphene, being confirmed by FTIR spectrum, facilitate the exfoliation of the graphite into graphene. The concentration of the graphene in the ethanol reached up to 1.44 mg mL-1 and the exfoliated suspension was relatively stable. The content of monolayer, bilayer, and multilayer in the exfoliated graphene suspension were 21%, 37%, and 42%, respectively. The as-prepared graphene sheets were free-defect. This novel approach may not only enable to exfoliate the graphite into graphene but also to make the graphene-curcumin hybrid which might find applications in pharmaceutical industry.

In this study, solution enhanced dispersion by supercritical fluids (SEDS) technique was applied for the preparation of 5-aminosalicylic acid (5-ASA) loaded Eudragit S100 (EU S100) nanoparticles. The effects of various process variables including pressure, temperature, 5-ASA concentration and solution flow rate on morphology, particle size, 5-ASA loading and entrapment efficiency of nanoparticles were investigated. Under the appropriate conditions, drug-loaded nanoparticles exhibited a spherical shape and small particle size with narrow particle size distribution. In addition, the nanoparticles prepared were characterized by X-ray diffraction, Differential scanning calorimetry and Fourier transform infrared spectroscopy analyses. The results showed that 5-ASA was imbedded into EU S100 in an amorphous state after SEDS processing and the SEDS process did not induce degradation of 5-ASA.