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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Materials Map under construction

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 (1/1 displayed)

  • 2020Effect of trehalose and melibiose on crystallization of amorphous paracetamol2citations

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Lipiäinen, Tiina
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Palomäki, Emmi A. K.
1 / 1 shared
Strachan, Clare J.
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2020

Co-Authors (by relevance)

  • Lipiäinen, Tiina
  • Palomäki, Emmi A. K.
  • Strachan, Clare J.
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article

Effect of trehalose and melibiose on crystallization of amorphous paracetamol

  • Yliruusi, Jouko K.
  • Lipiäinen, Tiina
  • Palomäki, Emmi A. K.
  • Strachan, Clare J.
Abstract

<p>This paper investigates the solid-state behavior of two-phase solid dispersions involving small molecules. The effect of two sugars, trehalose and melibiose, on the recrystallization of amorphous paracetamol, and vice versa, was investigated. The solid dispersions were prepared via heating and quench-cooling, and then stored at a temperature of 38.5 +/- 0.5 degrees C and relative humidities of 3 +/- 1% and 75 +/- 1%. X-ray powder diffraction (XRPD) confirmed that the solid dispersions were amorphous, while Fourier-transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) revealed that the solid dispersions were two-phase systems with drugrich and excipient-rich regions. XRPD was used to qualitatively and quantitatively study the crystallization of the components, and revealed that, despite the existence of two phases, the sugars hindered the crystallization of paracetamol. In contrast, once the paracetamol crystallization started, it accelerated the crystallization of the sugars. Overall, the study demonstrates that small-molecule solid-dispersions need not be single-phase to observe mutual influences between the components in crystallization behavior, and that these effects are likely mediated through interactions at the phase interfaces, as well as alterations in water sorption and mechanical effects.</p>

Topics
  • dispersion
  • amorphous
  • phase
  • differential scanning calorimetry
  • recrystallization
  • crystallization
  • infrared spectroscopy