The prepared NPs were evaluated for differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and in vitro release studies.
The particles were then analyzed for differential scanning calorimetry (DSC), X-ray diffraction (XRD), particle size, zeta potential and dissolution properties.
We describe an electrospray technique for in situ preparation, for differential scanning calorimetry study, of samples of molecular liquids quenched into the glassy state on extremely short time scales (hyperquenched).
For differential scanning calorimetric analysis, 2-3 mg of the PHA film was encapsulated in aluminum pans and analyzed with a Perkin-Elmer Pyris 1 DSC (Perkin-Elmer, Waltham, MA, USA) in the temperature range of -50 to 200°C at a heating rate of 20°C/min under nitrogen atmosphere.
With these three types of PCMs, four samples were prepared for differential scanning calorimeter (DSC) tests: three samples that solely contained one type of PCM (MC18, MC24 or MC28) and one sample that contained a 50 50 % mass proportion mix of MC18 and MC28, here termed as MC18_28.
For differential scanning calorimetry (DSC) measurements and for analyzing the pH-dependence of binding to Her2, aliquots of the protein samples were also dialyzed in PBS, pH 6.0.
For differential scanning fluorimetry assays, full-length human wild-type D70A, E96A, D70A/E96A, D210A, and D308A Aproteinseins were expressed as N-terminal-hexa His-SUMO fusions and prepared as previously described.
For differential scanning calorimetry (DSC), 2 mg mL 1 h USP11DU, hUSP15DU, and hUSP4DU were dialyzed into PBS buffer, 10 mM phosphate buffer, 2.7 mM KCl, 137 mM NaCl pH 7. Data were collected on a Microcal VP-DSC calorimeter at a scan rate of 1 °C min 1 with a low feedback mode/gain.
For differential scanning calorimetry (DSC) a TG-DSC instrument (Labsys, SETARAM, Lyon) was used and experiments were carried out over the temperature range from room temperature to 650 °C at a heating rate of 5 K/min under the flow of Ar gas.
Structural relaxation processes were studied by means of differential scanning calorimetry for a number of compositions belonging to the Se-rich sides of Se Te, Ge Se and As Se chalcogenide systems.
