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Pyris manager software

Manufactured by PerkinElmer
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Pyris Manager software is a data analysis and instrument control software designed for use with PerkinElmer's thermal analysis instruments. The software provides a user-friendly interface for managing and analyzing data from these instruments.

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Lab products found in correlation

Pyris 1, by PerkinElmer (5 mentions) Dsc 6000, by PerkinElmer (4 mentions) Pyris 1 tga, by PerkinElmer (3 mentions) Dsc 8000, by PerkinElmer (3 mentions) Intracooler 2, by PerkinElmer (2 mentions) Differential scanning calorimeter, by PerkinElmer (2 mentions) Dsc 4000, by PerkinElmer (2 mentions) Diamond dsc, by PerkinElmer (1 mentions) Dsc 8000 analyzer, by PerkinElmer (1 mentions) Pyris 1 dsc, by PerkinElmer (1 mentions) Pyris 1 tga system, by PerkinElmer (1 mentions) Dsc 4000 analyzer, by PerkinElmer (1 mentions) Tga 4000, by PerkinElmer (1 mentions) Spectrum two ft ir spectrometer, by PerkinElmer (1 mentions) Evols 10 instrument, by Zeiss (1 mentions) Model dsc7, by PerkinElmer (1 mentions)

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Pyris software (56 citations)

24 protocols using pyris manager software

1

Thermogravimetric Analysis of Samples

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A Perkin Elmer Pyris 1 thermogravimetric analyzer (TGA) equipped with Pyris manager software (PerkinElmer Life and Analytical Sciences, 719 Bridgeport Ave., Connecticut, USA) was used for thermogravimetric analyses of the samples. Each sample was weighed and heated from 20–220°C at a heating rate of 10°C/min under an inert nitrogen atmosphere and monitored for the percent weight loss with temperature increase.
Alshahrani S.M., Morott J.T., Alshetaili A.S., Tiwari R.V., Majumdar S, & Repka M.A. (2015). Influence of Degassing on Hot-Melt Extrusion Process. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 80, 43-52.
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2

Differential Scanning Calorimetry Analysis

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Differential scanning calorimetry (DSC) analysis was performed using Diamond DSC, PerkinElmer with Pyris manager software (PerkinElmer Life and Analytical Sciences, CT, USA). Approximately 5 mg of sample was weighed and hermetically sealed in an aluminum pan. An empty aluminum pan was used for reference. The heating rate was set at 10°C/min from 25°C to 150°C under an inert atmosphere of nitrogen at a flow rate of 20 mL/min.
Kallakunta V.R., Tiwari R., Sarabu S., Bandari S, & Repka M.A. (2018). Effect of formulation and process variables on lipid based sustained release tablets via continuous twin screw granulation: A comparative study. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 121, 126-138.
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3

Thermal and Gravimetric Characterization of Materials

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The thermal transitions were studied with a DSC-8000 analyzer from PerkinElmer, Inc. (Waltham, MA, USA), coupled to a cooling accessory Intracooler 2 also from PerkinElmer, Inc. Samples followed a thermal sequence as follows: a first ramp from −30 °C to 190 °C, then a cooling step to −30 °C with heating and cooling rates of 10 °C/min. The measurements were performed under a nitrogen atmosphere using a flow rate of 20 mL/min. Sample weight was around 3.0 mg, using an empty aluminum pan as reference. Calibration was performed using an indium sample. Measurements were performed, at least, in duplicate. Thermograms were analyzed using the Pyris Manager software (PerkinElmer, Inc., Waltham, MA, USA).
A 550-TA Instruments Thermogravimetric Analyzer (New Castle, DE, USA) was used to perform the thermogravimetric analysis (TGA) between 25 °C to 700 °C, at a heating rate of 10 °C/min under a nitrogen atmosphere. The obtained data were analyzed by means of the TA analysis software. Measurements were carried out in triplicate.
Figueroa-Lopez K.J., Prieto C., Pardo-Figuerez M., Cabedo L, & Lagaron J.M. (2023). Development and Characterization of Electrospun Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Biopapers Containing Cerium Oxide Nanoparticles for Active Food Packaging Applications. Nanomaterials, 13(5), 823.
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4

Thermal Analysis of KTP Formulations

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DSC was obtained using Perkin Elmer Pyris 1 DSC equipped with Pyris manager software (PerkinElmer Life and Analytical Sciences, 710 Bridgeport Ave., Connecticut, USA). Appoximately 2–4 mg of KTP, physical mixtures or extrudates were heated from 30°C to 200°C at heating rate of 10°C/min.
Ashour E.A., Kulkarni V., Almutairy B., Park J.B., Shah S., Majumdar S., Lian Z., Pinto E., Bi Y., Durig T., Martin S.T, & Repka M.A. (2015). Influence of Pressurized Carbon Dioxide on Ketoprofen-Incorporated Hot-Melt Extruded Low Molecular Weight Hydroxypropylcellulose. Drug development and industrial pharmacy, 42(1), 123-130.
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5

Thermal Stability Analysis of KTP and Polymers

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TGA studies were performed for KTP and polymers used in this study to determine their stability at the extrusion temperatures using a Perkin Elmer Pyris 1 TGA equipped with Pyris manager software (PerkinElmer Life and Analytical Sciences, 710 Bridgeport Ave., Connecticut, USA).
Ashour E.A., Kulkarni V., Almutairy B., Park J.B., Shah S., Majumdar S., Lian Z., Pinto E., Bi Y., Durig T., Martin S.T, & Repka M.A. (2015). Influence of Pressurized Carbon Dioxide on Ketoprofen-Incorporated Hot-Melt Extruded Low Molecular Weight Hydroxypropylcellulose. Drug development and industrial pharmacy, 42(1), 123-130.
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6

Thermal Analysis of Solid-State Materials

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DSC experiments on pure APG and optimized SDs were performed with the help of “DSC apparatus (DSC-8000, Perkin Elmer, Waltham, MA, USA)” with the temperature range of 30.0–400.0 °C at the heating rate of 10.0 °C/min. The flow rate of nitrogen was set at 20 ml/min. DSC apparatus was attached with an auto sampler and chiller. Accurately weighed amounts of the samples of pure APG and optimized SDs (approximately 3.0 mg) were taken and placed in an aluminium pan which was hermetically sealed. The software used for DSC data analysis was “Pyris Manager Software (Perkin Elmer, Waltham, MA, USA)”. DSC analysis was performed for the characterization of the solid state of materials (Alshehri et al., 2017a (link)).
Alshehri S.M., Shakeel F., Ibrahim M.A., Elzayat E.M., Altamimi M., Mohsin K., Almeanazel O.T., Alkholief M., Alshetaili A., Alsulays B., Alanazi F.K, & Alsarra I.A. (2018). Dissolution and bioavailability improvement of bioactive apigenin using solid dispersions prepared by different techniques. Saudi Pharmaceutical Journal : SPJ, 27(2), 264-273.
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7

Thermal Stability of KPR-Eudragit Mixtures

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The thermal stability of the starting materials (pure KPR, Pure Eudragit® E PO and physical mixtures which contains KPR ranged from 10–50% drug load) was studied using a PerkinElmer Pyris™ 1 TGA system. The Pyris™ Manager software (PerkinElmer Life and Analytical Sciences, Waltham, MA, USA) was used to operate the instrument and analyze the data. Under an inert nitrogen atmosphere at a flow rate of 20 mL/min, 3–4 mg of the sample was weighed and heated from 25 °C to 220 °C at 10 °C/min. Percent weight loss was plotted against temperature to determine the relationship between weight loss and temperature.
Alshetaili A.S., Almutairy B.K., Tiwari R.V., Morott J.T., Alshehri S.M., Feng X., Alsulays B.B., Park J.B., Zhang F, & Repka M.A. (2016). Preparation and Evaluation of Hot-Melt Extruded Patient-Centric Ketoprofen Mini-Tablets. Current drug delivery, 13(5), 730-741.
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8

Differential Scanning Calorimetry of OPT-NCC

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Approximately 4 mg of filtered and air-dried OPT-NCC (to constant mass) was placed into an aluminum pan and sealed. The pan was then placed directly into the furnace of a DSC 6000 PerkinElmer Differential Scanning Calorimeter (Waltham, MA, USA) and the data generated was analyzed using version 11 Pyris™ Manager Software (PerkinElmer). The temperature of the DSC was monitored with a computer and a controlled heating rate of 10 K/min was used for the analysis over the temperature range 30–150 °C. All DSC analyses were conducted in triplicate (n = 3) under a nitrogen atmosphere purged at a flow rate of 20 mL/min and the thermogram for the micro co-crystal (uncoated) was used as a reference.
Witika B.A., Smith V.J, & Walker R.B. (2020). Quality by Design Optimization of Cold Sonochemical Synthesis of Zidovudine-Lamivudine Nanosuspensions. Pharmaceutics, 12(4), 367.
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9

Thermal Analysis of MA, FFA, and Formulations

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DSC analysis of pure MA, FFA and eight different formulations were determined using “DSC apparatus (DSC-8000, Perkin Elmer, Waltham, MA)” over the temperature range of 25.00°C to 250.00°C at 10.00°C/min and recorded under a nitrogen purge of 20 ml/min. This instrument was equipped with auto sampler and chiller. The samples of interest were accurately weighed (around 3.0 mg) and placed in an aluminium pan and hermetically sealed. This instrument was equipped with Pyris manager software “(Perkin Elmer, Waltham, MA)” to evaluate the solid state characterization and thermal stability of each sample.
Alshehri S., Shakeel F., Ibrahim M., Elzayat E., Altamimi M., Shazly G., Mohsin K., Alkholief M., Alsulays B., Alshetaili A., Alshahrani A., Almalki B, & Alanazi F. (2017). Influence of the microwave technology on solid dispersions of mefenamic acid and flufenamic acid. PLoS ONE, 12(7), e0182011.
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10

Thermal Characterization of Nanocellulose Crystals

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Approximately 4 mg of ultra-filtered and dried NCC was placed into aluminum pans and sealed. The pans were then placed directly into the furnace of a DSC 6000 PerkinElmer Differential Scanning Calorimeter (Waltham, MA, USA) and the data analyzed using version 11 Pyris™ Manager Software (PerkinElmer, Waltham, MA, USA). The temperature of the DSC was monitored with a computer and a controlled heating rate of 10 K/min was used for the analysis over the temperature range 30–150 °C. Thermograms were acquired at a rate of 10 scans/cm−1. All DSC analyses were conducted in triplicate (n = 3) under a nitrogen atmosphere purged at a flow rate of 20 mL/min and the thermogram for the micro co-crystal was used for reference purposes.
Witika B.A., Smith V.J, & Walker R.B. (2020). A Comparative Study of the Effect of Different Stabilizers on the Critical Quality Attributes of Self-Assembling Nano Co-Crystals. Pharmaceutics, 12(2), 182.
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