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Dsc 50 cell

Manufactured by Shimadzu
Sourced in Japan

The DSC-50 cell is a thermal analysis instrument used to measure the heat flow associated with physical and chemical changes in a material as a function of temperature or time. It provides information about the thermal properties of a sample, such as phase transitions, glass transitions, and reactions.

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10 protocols using dsc 50 cell

1

Thermal Characterization of Samples

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The samples were subjected to differential and scanning calorimetry (DSC), thermogravimetry derivative (TG/DTG). The DSC curves were obtained on DSC-50 cell (Shimadzu) using aluminum sample holder with 2 mg of sample in an atmosphere of nitrogen (50 mL/min−1) and heating rate of 10°C min−1 in the temperature range from 25 to 500°C. The DSC cell was checked with indium (RM 156.6°C, ΔHmel = 28.54 Jg-1) and zinc (PF 419.6°C). The TG/DTG curves were obtained in thermobalance model TGA 50 (Shimadzu) using a temperature range of 25–900°C in a platinum sample holder with ~3 mg of sample under dynamic nitrogen atmosphere (50 mL/min−1) and heating rate of 10°C/min−1. The thermobalance was verified with CaC2O4·H2O.
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2

Thermal Characterization of Materials by DSC and TGA

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Differential scanning calorimetry (DSC) curves were obtained by a DSC-50 cell (Shimadzu, Kyoto, Japan) using aluminum crucibles. Approximately 2 mg of samples were put into these crucibles, and the measurements were made under a dynamic nitrogen atmosphere (50 mL/min) at a heating rate of 10 °C/min in the temperature range 25–600 °C. The DSC cell was calibrated with indium (melting point (m.p.) = 156.6 °C and fusion enthalpy (ΔHfus.) = 28.54 J/g) and zinc (m.p. = 419.6 °C). Thermogravimetric (TG/DTG) curves were obtained with the TGA-50 thermobalance (Shimadzu, Kyoto, Japan) using platinum crucibles that contained roughly 3 mg of a sample. These measurements were made under a dynamic nitrogen atmosphere (50 mL/min) at a heating rate of 10 °C/min in the temperature range 25–900 °C.
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3

Thermal Analysis of Material Samples

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Differential scanning calorimetry (DSC) thermal analysis was carried out in a DSC-50 cell Shimadzu® (Tokyo, Japan) using approximately 2 mg of sample in aluminum crucibles under dynamic nitrogen atmosphere (50 mL·min−1) and with a heating rate of 10 °C·min−1 at a temperature range of 30–500 °C.
Thermogravimetry (TG) was obtained using a TGA-50 Shimadzu® (Tokyo, Japan) in the temperature range of 30–900 °C, using alumina crucibles with approximately 2 mg of samples under dynamic nitrogen atmosphere (50 mL·min−1) and with a heating rate of 10 °C·min−1.
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4

Thermal and Morphological Analysis of Drug Compounds

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The differential scanning calorimetry (DSC) curves (OEFC, β-CD, MF, MA, and CE) were obtained using a DSC-50 cell (Shimadzu, Kyoto, Japan), at a heating rate of 10 °C/min, at 25–500 °C, under an N2 dynamic atmosphere (50 mL/min). An aluminum (Al) capsule containing approximately 2 mg of the sample was used in this assay. For the TG/DTG (thermogravimetry/derivative thermogravimetry) assays, a TGA-51 thermogravimetric analyzer (Shimadzu, Kyoto, Japan) was used at a temperature range of 25–500 °C, under a dynamic N2 atmosphere (50 mL/min). A platinum crucible (Pt) containing approximately 2 mg of the sample was used in this assay. For the MeV analysis, the samples were mounted in aluminum tubes, metallized with gold beams, and visualized in an electronic microscope (model JSM-6390-LV; JEOL, Peabody, MA, USA) under a voltage acceleration of 12 kV. The moisture content (OEFC, β-CD, MF, MA, and CE) was determined using the Karl Fischer method with the aid of a Titrino Plus KF 870 (Metrohm, Herisau, Switzerland), using methanol (Fluka, St. Louis, MO, USA) as the titration solution. The analyses were performed in triplicates [42 (link)].
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5

DSC Thermal Analysis of Samples

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DSC thermal analysis was carried out in a DSC-50 cell Shimadzu® (Tokyo, Japan) using approximately 2 mg of sample in aluminum crucibles under dynamic nitrogen atmosphere (50 mL·min−1) and heating rate of 10 °C∙min−1 at a temperature range of 30–500 °C. The temperature and heat flow of the DSC instrument was calibrated with indium (melting point = 157.5 °C and ∆H = 26.7 J·g−1).
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6

Thermal Analysis of Quercetin Formulations

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DSC curves of quercetin free and suspension were obtained in a DSC-50 cell (Shimadzu) using aluminum crucibles with about 2 mg of samples, under dynamic nitrogen atmosphere (50 mL min−1) and heating rate of 10 °C min−1 in the temperature range from 25 to 600 °C. The DSC cell was calibrated with indium (mp 156.6 °C; ΔHmelting = 28.54 J g−1) and zinc (mp 419.6 °C).
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7

Physicochemical Characterization of Nanoparticles

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Dynamic Light Scattering (DLS) technique was used to obtain the mean size and polydispersity index (PDI) of the nanoparticles. Zeta potentials of the nanoparticles were measured by a Malvern Zetasizer Nano S. Scanning electron microscopy (SEM) images were taken using a Inspect F50 microscope (FEI Company) with field emission guns. Liquid samples were dropped on aluminum stubs covered with carbon tape, dried at 40 • C for 2 h, metalized with gold in the secondary electron mode, and then analyzed at 20 kV. Lyophilized nanoparticles and raw materials (HRP, IAA, CS and HA) were analyzed by Fourier-transformed infrared spectroscopy (FTIR) in spectrophotometer Cary 630 (Agilent Technologies), equipped with a zinc selenide crystal (ZnSe) and ATR (total attenuated reflection) device. Thermogravimetric analysis (TGA) was performed in SDT equipment model Q600 (TA Instruments): heating flow 10 • C/min (35 • C-600 • C) under nitrogen atmosphere (10 mL/ min). Differential scanning calorimetry (DSC) was performed in DSC-50 cell (Shimadzu): heating flow 10 • C/min (30 • C-500 • C) under nitrogen atmosphere (50 mL/min).
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8

Thermal Analysis of Samples

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Thermogravimetric analysis (TGA) was carried out using an SDT equipment model Q600 (TA Instruments -Delaware, USA). About 5.0 mg of the samples were supported in an alumina crucible and analyzed using a flow rate of 10 mL/min, under inert nitrogen and heating flow of 10 • C/min, from 35 • C to 500 • C. Differential scanning calorimetry (DSC) was performed through the DSC-50 cell (Shimadzu -Kyoto, Japan), with a flow rate of 50 mL/min, under inert nitrogen, and heating rate of 10 • C/min from 35 to 500 • C. Samples (2.0 mg) were analyzed in closed aluminum capsules and an empty aluminum capsule was used as reference.
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9

Nanoparticle Characterization Protocol

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For the preparation of nanoparticles: Magnetic stirrer (C-MAG HS 7, IKA -Staufen, Germany), pHmeter (D-22, Digimed -São Paulo, Brazil). Determination of Particle size, polydispersity index, and zeta potential: Malvern Zetasizer Nano S (Malvern Instruments, Worcestershire, UK). Enzymatic activity: UV/Vis Spectrophotometer (Libra S22, Biochrom -Cambridge, UK), centrifuge (Rotina 380 R Benchtop, Andreas Hettich GmbH & Co. KG -Tuttlingen, Germany). For Fourier transform infrared spectroscopy (FTIR), Thermogravimetric and Differential scanning calorimetry (DSC) analyzes were used: Cary 630 Spectrophotometer (Agilent Technologies -California, USA), SDT equipment model Q600 (TA Instruments -Delaware, USA), DSC-50 cell (Shimadzu -Kyoto, Japan), respectively. For Scanning electron microscopy (SEM) was used an Inspect F50 microscope (FEI Company -Tokyo, Japan).
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10

Thermal Analysis of Inclusion Complexes

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The EOHM, b-CD, PM and of inclusion complexes samples were subjected to DSC test. The DSC curves were obtained using a DSC-50 cell, from Shimadzu, using a heating rate of 10 C/min. The DSC curves were obtained between 25 and 500 C under a dynamic atmosphere of N 2 (50 mL/min), employing aluminum capsules (Al) containing $2 mg of the samples. The DSC cell was calibrated with indium (melting point 156.6 C; DH fus = 28.54 J/g) and zinc (melting point 419.6 C).
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