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 (1/1 displayed)

  • 2014The influence of pressure on the intrinsic dissolution rate of amorphous indomethacin15citations

Places of action

Chart of shared publication
Wang, Wenbo
1 / 2 shared
Tsolakou, Theodosia
1 / 1 shared
Rades, Thomas
1 / 107 shared
Qiu, Danwen
1 / 2 shared
Löbmann, Korbinian
1 / 49 shared
Chart of publication period
2014

Co-Authors (by relevance)

  • Wang, Wenbo
  • Tsolakou, Theodosia
  • Rades, Thomas
  • Qiu, Danwen
  • Löbmann, Korbinian
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article

The influence of pressure on the intrinsic dissolution rate of amorphous indomethacin

  • Flouda, Konstantina
  • Wang, Wenbo
  • Tsolakou, Theodosia
  • Rades, Thomas
  • Qiu, Danwen
  • Löbmann, Korbinian
Abstract

<p>New drug candidates increasingly tend to be poorly water soluble. One approach to increase their solubility is to convert the crystalline form of a drug into the amorphous form. Intrinsic dissolution testing is an efficient standard method to determine the intrinsic dissolution rate (IDR) of a drug and to test the potential dissolution advantage of the amorphous form. However, neither the United States Pharmacopeia (USP) nor the European Pharmacopeia (Ph.Eur) state specific limitations for the compression pressure in order to obtain compacts for the IDR determination. In this study, the influence of different compression pressures on the IDR was determined from powder compacts of amorphous (ball-milling) indomethacin (IND), a glass solution of IND and poly(vinylpyrrolidone) (PVP) and crystalline IND. Solid state properties were analyzed with X-ray powder diffraction (XRPD) and the final compacts were visually observed to study the effects of compaction pressure on their surface properties. It was found that there is no significant correlation between IDR and compression pressure for crystalline IND and IND-PVP. This was in line with the observation of similar surface properties of the compacts. However, compression pressure had an impact on the IDR of pure amorphous IND compacts. Above a critical compression pressure, amorphous particles sintered to form a single compact with dissolution properties similar to quench-cooled disc and crystalline IND compacts. In such a case, the apparent dissolution advantage of the amorphous form might be underestimated. It is thus suggested that for a reasonable interpretation of the IDR, surface properties of the different analyzed samples should be investigated and for amorphous samples the IDR should be measured also as a function of the compression pressure used to prepare the solid sample for IDR testing.</p>

Topics
  • impedance spectroscopy
  • surface
  • amorphous
  • grinding
  • glass
  • glass
  • milling