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Dsc 60 differential scanning calorimeter

Manufactured by Shimadzu
Sourced in Japan

The Shimadzu DSC-60 is a differential scanning calorimeter that measures the thermal properties of materials. It can detect and analyze phase transitions, glass transitions, and other thermal events in solid and liquid samples.

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7 protocols using dsc 60 differential scanning calorimeter

1

Characterization of Polymer Nanomaterials

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1H NMR spectra were obtained from a Bruker ARX 400 MHz spectrometer at room temperature with tetramethylsilane (TMS) as the internal standard. The GPC analysis was conducted with a HLC-8320GPC (TOSOH, Japan) instrument at 30 °C at a flow rate of 0.3 mL/min. The solid-state 13C CP/MAS NMR measurements were carried out at 75 MHz with a spinning rate of 5 kHz at room temperature using a Bruker AV-300 NMR spectrometer. The chemical shifts were referred to an external adamantane standard. Wide angle X-ray diffraction (WXRD) patterns were recorded on a Shimadzu XD-D1 X-ray diffractometer with Ni-filtered Cu Kα (1.54 Å) radiation (20 kV, 40 mA). Powder samples were scanned from 2θ = 4.5–60° at a speed of 5°/min. FTIR spectra were measured using a Shimadzu IR Prestige-21 FTIR spectrometer at room temperature using the KBr pellet method. TGA analysis was performed with using a TA SDT 2960 instrument at a heating rate of 10 °C/min from room temperature to 500 °C in a nitrogen atmosphere. DSC measurements were measured on a SHIMADZU DSC-60 differential scanning calorimeter with a scanning temperature range from 20–80 °C at a scanning rate of 10 °C/min. The transmission electron microscopy image was observed using a JEM 1200EX (JEOL) transmission electron microscope operating at 120 KV.
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2

Differential Scanning Calorimetry of Nanostructured Lipid Carriers

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Differential scanning calorimetry is a thermal test that measures the physical properties of the sample in terms of temperature. This analysis is considered as one of the main analyses in determining the characteristics of a nanostructured lipid carrier. Enthalpy and melting point are some of the information that can be obtained from this analysis.22 (link) DSC analysis was performed using a DSC-60 differential scanning calorimeter (Shimadzu, Japan).
The samples weighed accurately were placed in aluminum pans and sealed with a lid. In the scanning process, a heating rate of 5°C was applied in the temperature range from 20°C to 180°C with a nitrogen purge of 0.2 mL/min.
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3

Thermal Analysis of Nanoparticle Interactions

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The DSC thermograms (GA, zein, phospholipid, SA, VA, sucrose, the lyophilized GA-CACNP/VA, and its physical mixture) were examined to detect the thermotropic behavior, the level of crystallinity, and the possible interactions between different components of the NPs. Briefly, each sample (5 mg) was heated in a hermetically sealed aluminium pan at a rate of 10°C/min from 50°C to 300°C under a nitrogen purge of 30 mL/min using a DSC-60 differential scanning calorimeter (Shimadzu, Kyoto, Japan).47 (link)
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4

Thermal Analysis of Gliclazide Cubosomal Formulations

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DSC thermograms of gliclazide-loaded cubosomal particles, blank cubosomal particles, plain gliclazide, GMO, and P407 were examined using a DSC-60 differential scanning calorimeter (Shimadzu, Kyoto, Japan). Each sample (5 mg) was heated in an aluminum pan from 30 to 320 °C at a constant rate of 10 °C/min under a nitrogen purge of 30 mL/min. A similar empty pan was used as the reference.
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5

Thermal Characterization of Protein Dispersions

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Differential scanning calorimetry was used to determine the onset (T onset ) temperature, peak temperature (T p ), and end set temperature (T end ) for sonicated and untreated protein dispersions.
The DSC thermograms of the samples were registered using a Shimadzu DSC-60 differential scanning calorimeter (Shimadzu, Kyoto, Japan). The instrument was calibrated with indium (156.6 °C), lead (327.5 °C) and zinc (419.6 °C). Samples (2.88 mg) were hermetically sealed in aluminum pans and heated from 25 to 135°C at a scanning rate of 10°C/min under a nitrogen atmosphere. An empty aluminum pan of equal weight was used as the reference.
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6

DSC Analysis of Glass Transition

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Glass transition temperature (Tg) measurement was performed using Differential Scanning Calorimeter (DSC‐60, Shimadzu, Kyoto, Japan) according to Coronado Jorge et al. (2015) and Bonilla, Bittante, and Sobral (2017) with some adjustments. About 2 mg of developed films were placed in hermetically sealed aluminum pans and heated from − 100 C to + 200°C at a heating rate of 10°C/min, after cooling with liquid nitrogen as a cryogenic. Tg was obtained from the temperature fluctuation point of the temperature.
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7

Thermal Analysis of Drug Formulations

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A Differential Scanning Calorimeter (DSC-60, Shimadzu, Japan) connected to a computerized thermal analyzer was used to obtain DSC thermograms of the KT, eudragit RL 100, gelatin, 1:1 physical mixtures and thermal behavior of the drug in nanoparticles. Analyzed the drug's endothermal transition using thermo gravimetry 33 .
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