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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Royall, Paul G.

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King's College London

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2023Computer numerical control (CNC) carving as an on-demand point-of-care manufacturing of solid dosage form4citations
  • 2019Ocular anti-inflammatory activity of prednisolone acetate loaded chitosan-deoxycholate self-assembled nanoparticles47citations
  • 2012Immersion mode material pocket dynamic mechanical analysis (IMP-DMA): A novel tool to study gelatinisation of purified starches and starch-containing plant materials9citations
  • 2012Identification and molecular interpretation of the effects of drug incorporation on the self-emulsification process using spectroscopic, micropolarimetric and microscopic measurements5citations
  • 2009Monitoring crystallisation of drugs from fast-dissolving oral films with isothermal calorimetry26citations
  • 2005Biocompatible polymer blends: Effects of physical processing on the molecular interaction of poly(vinyl alcohol) and poly(vinyl pyrrolidone)29citations
  • 2001Characterization of amorphous ketoconazole using modulated temperature differential scanning calorimetry14citations
  • 2001Characterization of amorphous ketoconazole using modulated temperature differential scanning calorimetry14citations

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Kaba, Kazim
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Alqurshi, Abdulmalik
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Hanafy, Ahmed F.
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Gabr, Khairy E.
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Saunders, Mark
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Martin, G. P.
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Jones, Stuart
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Craig, Duncan Q. M.
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Mooter, Guy Van Den
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Co-Authors (by relevance)

  • Kaba, Kazim
  • Purnell, Bryn
  • Liu, Yujing
  • Alhnan, Mohamed A.
  • Alqurshi, Abdulmalik
  • Abdalla, Ahmed M.
  • Hanafy, Ahmed F.
  • Gabr, Khairy E.
  • Guda, Tawheda K.
  • Ellis, Peter Rory
  • Warren, Frederick J.
  • Butterworth, Peter J.
  • Barker, Sa
  • Mercuri, A.
  • Belton, Ps
  • Gaisford, Simon
  • Verma, Amit
  • Saunders, Mark
  • Martin, G. P.
  • Jones, Stuart
  • Brown, M. B.
  • Craig, Duncan Q. M.
  • Mooter, Guy Van Den
  • Van Den Mooter, Guy
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article

Characterization of amorphous ketoconazole using modulated temperature differential scanning calorimetry

  • Craig, Duncan Q. M.
  • Mooter, Guy Van Den
  • Royall, Paul G.
Abstract

The objective of the present study was to characterize the glassy state of ketoconazole and to calculate its molecular mobility below the glass transition, with a view to further developing the use of modulated temperature differential scanning calorimetry (MTDSC) as a means of studying relaxation behavior. Particular emphasis is placed on identifying the influence of the choice of experimental parameters on the measured values of both the glass transition temperature (Tg) and the relaxation enthalpy magnitude. Amorphous ketoconazole was studied using an amplitude of +-0.212 K, a period of 40 s, and an underlying heating rate of 2 K/min. The correction required for the calculation of the relaxation endotherm magnitude (the 'Tg shift effect') was demonstrated and is discussed in terms of the mechanism underpinning this phenomenon. Similarly, the influence of the choice of MTDSC experimental parameters on the measured Tg was studied by varying the amplitude from +-0.011 to +-0.424 K and the period from 25 to 50 s. The influence of the cooling rate from the melt on the magnitude of the relaxation endotherm and position of the glass transition was investigated. It was noted that the magnitude of the relaxation endotherm increased with slower cooling rates, this being ascribed to a combination of annealing during the cooling and heating cycle and a further facet of the Tg shift effect. Annealing experiments were performed at aging temperatures Tg-12-Tg-42 K for periods ranging from 10 min up to 16 h. The relaxation behavior was characterized by fitting the calculated extent of relaxation to the Williams-Watts equation. Overall, the study has highlighted theoretical and experimental issues that need to be considered when using both DSC and MTDSC for the calculation of relaxation times.

Topics
  • impedance spectroscopy
  • amorphous
  • mobility
  • experiment
  • melt
  • glass
  • glass
  • thermogravimetry
  • glass transition temperature
  • differential scanning calorimetry
  • aging
  • annealing
  • aging