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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1.080 Topics available

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2024Influence of co-solvents on properties of terpene-based eutectic mixtures3citations
  • 2023Protease-Responsive Hydrogel Microparticles for Intradermal Drug Delivery8citations
  • 2013In vitro cross-linking of elastin peptides and molecular characterization of the resultant biomaterials19citations
  • 2009Better understanding of dissolution behaviour of amorphous drugs by in situ solid-state analysis using Raman spectroscopy123citations
  • 2007Screening for differences in the amorphous state of indomethacin using multivariate visualization104citations

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Chart of shared publication
Rades, Thomas
2 / 107 shared
Czyrski, Grzegorz S.
1 / 1 shared
Noddeland, Heidi K.
1 / 2 shared
Caruso, Frank
1 / 16 shared
Petersson, Karsten
1 / 4 shared
Lind, Marianne
1 / 1 shared
Malmsten, Martin
1 / 4 shared
Keeley, Fred W.
1 / 1 shared
Sippl, Wolfgang
1 / 1 shared
Neubert, Reinhard H. H.
1 / 1 shared
Schmelzer, Christian E. H.
1 / 2 shared
Jahreis, Günther
1 / 1 shared
Ruttkies, Christoph K. H.
1 / 1 shared
Wichapong, Kanin
1 / 1 shared
Schräder, Christoph U.
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Peltonen, L.
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Strachan, C.
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Yliruusi, J.
1 / 1 shared
Savolainen, M.
1 / 1 shared
Kogermann, K.
1 / 1 shared
Aaltonen, J.
1 / 2 shared
Gordon, Keith C.
1 / 14 shared
Sandler, Niklas
1 / 5 shared
Strachan, Clare
1 / 5 shared
Yliruusi, Jouko
1 / 13 shared
Savolainen, Marja
1 / 2 shared
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2024
2023
2013
2009
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Co-Authors (by relevance)

  • Rades, Thomas
  • Czyrski, Grzegorz S.
  • Noddeland, Heidi K.
  • Caruso, Frank
  • Petersson, Karsten
  • Lind, Marianne
  • Malmsten, Martin
  • Keeley, Fred W.
  • Sippl, Wolfgang
  • Neubert, Reinhard H. H.
  • Schmelzer, Christian E. H.
  • Jahreis, Günther
  • Ruttkies, Christoph K. H.
  • Wichapong, Kanin
  • Schräder, Christoph U.
  • Peltonen, L.
  • Strachan, C.
  • Yliruusi, J.
  • Savolainen, M.
  • Kogermann, K.
  • Aaltonen, J.
  • Gordon, Keith C.
  • Sandler, Niklas
  • Strachan, Clare
  • Yliruusi, Jouko
  • Savolainen, Marja
OrganizationsLocationPeople

article

Influence of co-solvents on properties of terpene-based eutectic mixtures

  • Rades, Thomas
  • Czyrski, Grzegorz S.
  • Heinz, Andrea
Abstract

<p>Terpene-based eutectic mixtures (EMs) are attractive platforms for transdermal delivery due to their solubilizing potential and ability to alter the barrier function of the stratum corneum (SC). Despite this, little is known about the effect of diluting EMs with co-solvents (CSs) on their solubility- and permeation-enhancing properties. Furthermore, insufficient attention has been paid on comparing these platforms with traditional solvents, such as propylene glycol (PG) or ethanol (EtOH). To address this gap, the present study investigates the impact of CS content in EM:CS blends on the transdermal delivery of clotrimazole (CLOT). Two CSs, propylene glycol and ethanol, and two terpene-based EMs, menthol:thymol and thymol:β-citronellol, were used. Each of the EMs was investigated at two different molar ratios between the terpenes, with one being their eutectic point, to explore its potential benefit for skin permeation. At each step, properties of the blends were compared with those of pure CSs. The EM:CS blends showed a better solubilizing potential for CLOT than EMs or CSs on their own. A higher content of CSs in the blends resulted in a higher skin permeation and retention of CLOT, and a lower degree of disarrangement of the SC structure. Furthermore, the blends of EMs at their EPs led to overall poorer permeation profiles, implying that the permeation rate is more affected by the individual terpenes than by the specific ratio at the eutectic point between them. In conclusion, addition of CSs to the EMs promotes permeation and retention of CLOT, while reducing the skin impairment caused by the terpenes.</p>

Topics
  • impedance spectroscopy