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Dsc 821e

Manufactured by Mettler Toledo
Sourced in Switzerland, Germany, United States

The DSC 821e is a differential scanning calorimeter (DSC) instrument designed for thermal analysis. It measures the heat flow associated with physical and chemical changes in materials as a function of temperature and time. The DSC 821e provides accurate and precise measurements of phase transitions, glass transitions, and other thermal events in a wide range of materials.

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62 protocols using dsc 821e

1

Thermal Analysis of Material Components

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DSC analysis of each component and product was performed using a Mettler Toledo DSC 821e (Mettler-Toledo GmbH, Greifensee, Switzerland) using STARe software (version 9.30, Mettler-Toledo GmbH, Greifensee, Switzerland). The instrument was calibrated using indium. During the tests, the heating rate was 5 °C min−1, and 10 L h−1 of Argon gas was used as the purge gas. In our studies for different purposes, we used several temperature ranges (25–140 °C; 25–110 °C, followed by recooling and reheating to 140 °C). The weight of our test samples ranged from 2 to 5 mg in each case. Assays were performed using a 40 μL covered aluminium sample holder with 3 holes.
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2

Thermal Analysis of Powder Samples

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The thermal analysis was performed by using Mettler Toledo DSC 821e (Mettler Inc., Schwerzenbach, Switzerland). About 3–5 mg of powder was placed into DSC sample pans, which were hermetically sealed but lid pierced. An empty pan was used as a reference in an inert atmosphere under constant argon purge. The samples were examined in the temperature interval of 25–300 °C at a heating rate of 5 °C min–1.
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3

Kinetics of Curing Behavior by DSC

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The cure kinetics of the prepared samples was monitored by DSC in non-isothermal scans at 2, 5, 10, 15 and 20 °C/min and isothermal scans at the temperatures of 50 °C, 70 °C, 80 °C and 90 °C. The equipment used was a Mettler-Toledo DSC 821e differential scanning calorimeter (Mettler Toledo AG, Analytical, Schwerzenbach, Switzerland) equipped with a sample robot and Haake EK90/MT intracooler (Thermo Electron GmbH, Karlsruhe, Germany). Additional isothermal scans at the temperature of 50 °C were made using a stochastic temperature modulated DSC technique, TOPEM (Mettler-Toledo DSC 823e, Schwerzenbach, Switzerland), in order to determine the vitrificationtime [39 ,40 ]. All DSC curing experiments were performed with a dry nitrogen gas flow of 50 mL/min, and the DSC was calibrated for both heat flow and temperature using indium. The data evaluation was performed with the STARe software (Mettler Toledo AG, Schwerzenbach, Switzerland). For all the experiments, a small sample, of about 8–10 mg for standard DSC and about 20 mg for TOPEM, was weighed into an aluminum pan, sealed and immediately inserted into the DSC furnace, which was previously heated either to the start temperature for non-isothermal scans or to the curing temperature for isothermal experiments, whereupon the curing experiment was immediately started.
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4

Thermal Analysis of Material Samples

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DSC analyses were performed using an automatic thermal analyzer Mettler Toledo DSC821e (Mettler-Toledo S.p.A., Milano, Italy) and an indium standard for temperature calibrations. Holed aluminum pans were employed in the experiments for all samples, and an empty pan, prepared in the same way, was used as a reference. Samples of 3–6 mg were weighted directly into the aluminum pans, and the thermal analyses of samples were conducted, at a heating rate of 5 °C/min, from 25 to 200 °C.
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5

Thermal Analysis of SEPI-Loaded NLCs

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DSC study was performed using a Mettler DSC 821e (Mettler-Toledo, Gießen, Germany). The scanning was performed at a heating rate of 5°C/min in 0°C–200°C under 5 mL/min nitrogen flow rate and compared with an empty aluminum pan as reference.18 (link) Samples involved in bulk PRES, SEPI alone, lyophilized drug-free NLCs, and lyophilized SEPI-NLCs. The thermograms of samples and the calorimetric parameters were calculated by STARe software.
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6

Drying Time and Thermal Analysis of FFSs

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Drying time is an important parameter of the FFSs. If the preparations need less time to dry, patient compliance is better. After drying, a compact flexible film layer is formed, which is not greasy and does not smear on the skin. During the experiment, the preparation was placed onto the PVA-based artificial skin. After the top of the layer seemed dry, a microscope slide was placed on the top of the formulation without pressure. If the formulation did not leave a mark on the slide, it meant that the film was dry. This was the drying time of the film. If the film was not dry, the test was repeated until we got a dry film [28 ].
The drying mechanism of the different FFSs was measured by DSC (Mettler-Toledo DSC 821e, Columbus, OH, USA). The measurement was performed in an argon and nitrogen atmosphere. 15–20 mg of samples was laid in 40-μL aluminum pans and small holes were made on the tops. The temperature was increased from 25 °C to 150 °C by 10 °C per minute.
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7

Thermal Analysis of Polymer Transitions

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Tg' and Tcry were analyzed with a Mettler Toledo DSC 821e (Gießen, Germany). 30 μL sample in 40 μL aluminum crucibles were cooled down to −60°C and heated to + 20°C at 10, 2.5, 1.0, or 0.5°C/min. The heating curves were analyzed for Tg'—as the midpoint of the transition—and Tcry peaks.
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8

Thermal Analysis of Genistein

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The DSC measurements were conducted by using the Mettler Toledo DSC 821e thermal analysis system with STARe thermal analysis program v. 9.1 (Mettler Inc., Schwerzenbach, Switzerland). Approximately 2–5 mg of genistein or its product was examined in the temperature range between 25°C and 350°C. The heating rate was 5°C min−1. Argon was used as carrier gas, at a flow rate of 10 L h−1 during the DSC investigation.
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9

Thermal Behavior Analysis of Polyesters

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Differential scanning
calorimetry (DSC) (Mettler Toledo DSC 821e) was used to investigate
the melting point of synthesized products and the thermal behavior
of polyesters in the range of −10 to 250 °C under N2 gas flow (50 cm3/min) with heating and cooling
rates of 10 °C/min.
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10

Differential Scanning Calorimetry Characterization

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The DSC curves were collected with a Mettler Toledo DSC 821e apparatus (Mettler Toledo AG, Greifensee, Switzerland) in the temperature interval of 25–300 °C with an Ar gas intake of 10 L/h. Heating was linear with a heating rate of 10 °C/min. The mass of the samples was between 3 and 5 mg in a 40 µL Al sample holder.
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