Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2012Quantification of process induced disorder in milled samples using different analytical techniquescitations
  • 2012The influence of milling on the dissolution performance of simvastatincitations

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Chart of shared publication
Gordon, Keith C.
2 / 14 shared
Rades, Thomas
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Mcgoverin, Cushla M.
1 / 1 shared
Zimper, Ulrike
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Aaltonen, Jaakko
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Strachan, Clare J.
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2012

Co-Authors (by relevance)

  • Gordon, Keith C.
  • Rades, Thomas
  • Mcgoverin, Cushla M.
  • Zimper, Ulrike
  • Aaltonen, Jaakko
  • Strachan, Clare J.
OrganizationsLocationPeople

article

Quantification of process induced disorder in milled samples using different analytical techniques

  • Gordon, Keith C.
  • Rades, Thomas
  • Krauel-Goellner, Karen
  • Mcgoverin, Cushla M.
  • Zimper, Ulrike
  • Aaltonen, Jaakko
Abstract

The aim of this study was to compare three different analytical methods to detect and quantify the amount of crystalline disorder/ amorphousness in two milled model drugs. X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC) and Raman spectroscopy were used as analytical methods and indomethacin and simvastatin were chosen as the model compounds. These compounds partly converted from crystalline to disordered forms by milling. Partial least squares regression (PLS) was used to create calibration models for the XRPD and Raman data, which were subsequently used to quantify the milling-induced crystalline disorder/ amorphousness under different process conditions. In the DSC measurements the change in heat capacity at the glass transition was used for quantification. Differently prepared amorphous indomethacin standards (prepared by either melt quench cooling or cryo milling) were compared by principal component analysis (PCA) to account for the fact that the choice of standard ultimately influences the quantification outcome. Finally, the calibration models were built using binary mixtures of crystalline and quench cooled amorphous drug materials. The results imply that the outcome with respect to crystalline disorder for milled drugs depends on the analytical method used and the calibration standard chosen as well as on the drug itself. From the data presented here, it appears that XRPD tends to give a higher percentage of crystalline disorder than Raman spectroscopy and DSC for the same samples. For the samples milled under the harshest milling conditions applied (60 min, sixty 4 mm balls, 25 Hz) a crystalline disorder/ amorphous content of 44.0% (XRPD), 10.8% (Raman spectroscopy) and 17.8% (DSC) were detected for indomethacin. For simvastatin 18.3% (XRPD), 15.5% (Raman spectroscopy) and 0% (DSC, no glass transition) crystalline disorder/ amorphousness were detected.

Topics
  • compound
  • amorphous
  • melt
  • grinding
  • glass
  • glass
  • milling
  • differential scanning calorimetry
  • Raman spectroscopy
  • heat capacity