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 (5/5 displayed)

  • 2012Quantification of process induced disorder in milled samples using different analytical techniquescitations
  • 2012The influence of milling on the dissolution performance of simvastatincitations
  • 2009Formation kinetics and stability of carbamazepine-nicotinamide cocrystals prepared by mechanical activation80citations
  • 2009Quantitative solid-state analysis of three solid forms of ranitidine hydrochloride in ternary mixtures using Raman spectroscopy and X-ray powder diffraction50citations
  • 2005Characterization of polymorphic solid-state changes using variable temperature X-ray powder diffraction43citations

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Gordon, Keith C.
2 / 14 shared
Rades, Thomas
4 / 107 shared
Krauel-Goellner, Karen
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Mcgoverin, Cushla M.
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Zimper, Ulrike
2 / 2 shared
Strachan, Clare J.
1 / 10 shared
Hubert, Madlen
1 / 1 shared
Chieng, Norman
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Saville, Dorothy
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Rehder, Sönke
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Rantanen, Jukka
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Yliruusi, Jouko
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Airaksinen, Sari
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Karjalainen, Milja
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Co-Authors (by relevance)

  • Gordon, Keith C.
  • Rades, Thomas
  • Krauel-Goellner, Karen
  • Mcgoverin, Cushla M.
  • Zimper, Ulrike
  • Strachan, Clare J.
  • Hubert, Madlen
  • Chieng, Norman
  • Saville, Dorothy
  • Rehder, Sönke
  • Rantanen, Jukka
  • Yliruusi, Jouko
  • Airaksinen, Sari
  • Karjalainen, Milja
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article

Formation kinetics and stability of carbamazepine-nicotinamide cocrystals prepared by mechanical activation

  • Hubert, Madlen
  • Chieng, Norman
  • Rades, Thomas
  • Saville, Dorothy
  • Aaltonen, Jaakko
Abstract

<p>Co-milling of various carbamazepine (CBZ) polymorphic forms (form I, III and dihydate) with nicotinamide (NIC) was performed in this study to investigate the formation kinetics of carbamazepine-nicotinamide cocrystals (CBZ-NIC) and to evaluate their physical stability. Milling was carried out at room temperature using an oscillatory ball mill at a 1:1 molar ratio of CBZ and NIC for various times up to 60 min. A freshly prepared sample was used for each milling. In the stability study, the milled samples (4, 10, 15, and 30 min) were stored under four conditions (20 and 40 °C; 33 and 75%RH) for up to four weeks. Samples were analyzed by X-ray powder diffraction (XRPD) and differential scanning calorimetry. XRPD showed that all CBZ forms used in this study formed cocrystals when co-milled with NIC (characteristic XRPD peaks at 6.6, 8.9, 10.1, 20.4, and 26.5 °2θ). Cocrystal formation was qualitatively found to be fastest for CBZ dihydrate (CBZ DH, ̃1 min), followed by CBZ form I (̃6 min), and CBZ form III (̃15 min). Upon storage, cocrystals formed from CBZ DH were found to be physically stable under all conditions studied, regardless of a small amount of impurity. For the two anhydrous forms (CBZ I and III), the physical stability of the co-milled CBZ-NIC samples was dependent on the duration of milling, the relative humidity, and temperature of the storage conditions. Under "mild" storage conditions (i.e., 20 °C/33%RH), either partially or fully formed CBZ-NIC cocrystals were found to revert back to pure CBZ and NIC. Under "moderate" storage conditions (i.e., 20 °C/75%RH and 40 °C/33%RH), CBZ-NIC cocrystals reverting to pure CBZ and NIC would occur initially, followed by cocrystal formation with increasing storage time. On the other hand, "stress" storage conditions (i.e., 40 °C/75%RH) were found to be ideal for cocrystal formation and stability. Moisture has been found to favor cocrystallization. Water molecules appear to have a significant effect on the formation (water molecules from CBZ DH) and the stability (high humidity) of the CBZ-NIC cocrystal. The "purity" of the cocrystal samples (i.e., presence of CBZ and/or NIC seeds) can affect the physical stability of CBZ-NIC cocrystals prepared by mechanical activation.</p>

Topics
  • grinding
  • milling
  • differential scanning calorimetry
  • activation