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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Murnane, Darragh

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University of Hertfordshire

in Cooperation with on an Cooperation-Score of 37%

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Publications (5/5 displayed)

  • 2023Combining branched copolymers with additives generates stable thermoresponsive emulsions with in situ gelation upon exposure to body temperature3citations
  • 2019MicroCoat™: Improved Drug Release Control For Sustained Release Multiparticulatescitations
  • 2018Investigation into the internal structure of coated microparticles to support formulation and coating process developmentcitations
  • 2015Formulation pre-screening of inhalation powders using computational atom-atom systematic search method48citations
  • 2013Rapid characterisation of the inherent dispersibility of respirable powders using dry dispersion laser diffraction55citations

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Pavlova, Ewa
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Cook, Mt
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Mahmoudi, Najet
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Rajbanshi, Abhishek
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Dreiss, Cécile A.
1 / 16 shared
Slouf, Miroslav
1 / 6 shared
Richardson, Craig
2 / 2 shared
Liu, Fang
2 / 20 shared
Patel, Kavil
2 / 3 shared
Scott, Nathan
1 / 1 shared
Mohylyuk, Valentyn
2 / 6 shared
Hammond, Robert B.
1 / 1 shared
Soufian, Majeed
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Pencheva, Klimentina
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Roberts, Kevin J.
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Ramachandran, Vasuki
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Pickering, Jonathan
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Martin, Gary P.
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Jaffari, Sara
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Collins, Elizabeth
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Forbes, Ben
2 / 3 shared
Barlow, David J.
1 / 3 shared
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2019
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Co-Authors (by relevance)

  • Pavlova, Ewa
  • Cook, Mt
  • Mahmoudi, Najet
  • Rajbanshi, Abhishek
  • Dreiss, Cécile A.
  • Slouf, Miroslav
  • Richardson, Craig
  • Liu, Fang
  • Patel, Kavil
  • Scott, Nathan
  • Mohylyuk, Valentyn
  • Hammond, Robert B.
  • Soufian, Majeed
  • Pencheva, Klimentina
  • Roberts, Kevin J.
  • Ramachandran, Vasuki
  • Pickering, Jonathan
  • Martin, Gary P.
  • Jaffari, Sara
  • Collins, Elizabeth
  • Forbes, Ben
  • Barlow, David J.
OrganizationsLocationPeople

document

Rapid characterisation of the inherent dispersibility of respirable powders using dry dispersion laser diffraction

  • Murnane, Darragh
  • Barlow, David J.
  • Martin, Gary P.
  • Jaffari, Sara
  • Collins, Elizabeth
  • Forbes, Ben
Abstract

Understanding and controlling powder de-agglomeration is of great importance in the development of dry powder inhaler (DPI) products. Dry dispersion laser diffraction measures particle size readily under controlled dispersing conditions, but has not been exploited fully to characterise inherent powder dispersibility. The aim of the study was to utilise particle size-dispersing pressure titration curves to characterise powder cohesivity and ease of de-agglomeration. Seven inhaled drug/excipient powders (beclometasone dipropionate, budesonide, fluticasone propionate, lactohale 300, salbutamol base, salmeterol xinafoate and tofimilast) were subjected to a range of dispersing pressures (0.2–4.5 Bar) in the Sympatec HELOS/RODOS laser diffractometer and particle size measurements were recorded. <br/>Particle size-primary pressure data were used to determine the pressures required for complete deagglomeration. The latter were employed as an index of the cohesive strength of the powder (critical primary pressure; CPP), and the curves were modelled empirically to derive the pressure required for 50% de-agglomeration (DA50). The powders presented a range of CPP (1.0–3.5 Bar) and DA50 (0.23–1.45 Bar) which appeared to be characteristic for different mechanisms of powder de-agglomeration. This approach has utility as a rapid pre-formulation tool to measure inherent powder dispersibility, in order to direct the development strategy of DPI products.

Topics
  • impedance spectroscopy
  • dispersion
  • strength
  • titration