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 (2/2 displayed)

  • 2015Lysozyme-magnesium aluminum silicate microparticles: Molecular interaction, bioactivity and release studies5citations
  • 2013Nicotine-magnesium aluminum silicate microparticle surface modified with chitosan for mucosal delivery18citations

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Chart of shared publication
Pongjanyakul, Thaned
2 / 7 shared
Rades, Thomas
2 / 107 shared
Puttipipatkhachorn, Satit
2 / 6 shared
Medlicott, Natalie J.
1 / 2 shared
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2015
2013

Co-Authors (by relevance)

  • Pongjanyakul, Thaned
  • Rades, Thomas
  • Puttipipatkhachorn, Satit
  • Medlicott, Natalie J.
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article

Nicotine-magnesium aluminum silicate microparticle surface modified with chitosan for mucosal delivery

  • Pongjanyakul, Thaned
  • Rades, Thomas
  • Puttipipatkhachorn, Satit
  • Kanjanakawinkul, Watchara
Abstract

Magnesium aluminum silicate (MAS), a negatively charged clay, and nicotine (NCT), a basic drug, can interact electrostatically to form microparticles. Chitosan (CS) was used for the surface modification of the microparticles, and a lyophilization method was used to preserve the original particle morphology. The microparticles were characterized in terms of their physicochemical properties, NCT content, mucoadhesive properties, and release and permeation across porcine esophageal mucosa. The results showed that the microparticles formed via electrostatic interaction between MAS and protonated NCT had an irregular shape and that their NCT content increased with increasing NCT ratios in the microparticle preparation solution. High molecular weight CS (800 kDa) adsorbed to the microparticle surface and induced a positive surface charge. CS molecules intercalated into the MAS silicate layers and decreased the crystallinity of the microparticles, leading to an increase in the release rate and diffusion coefficient of NCT from the microparticles. Moreover, the microparticle surface modified with CS was found to have higher NCT permeation fluxes and mucoadhesive properties, which indicated the significant role of CS for NCT mucosal delivery. However, the enhancement of NCT permeation and of mucoadhesive properties depended on the molecular weight and concentration of CS. These findings suggest that NCT-MAS microparticle surface modified with CS represents a promising mucosal delivery system for NCT.

Topics
  • morphology
  • surface
  • Magnesium
  • Magnesium
  • aluminium
  • molecular weight
  • crystallinity