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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University of Tartu

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2015Diagnostic and clinical significance of Crohn’s disease-specific anti-MZGP2 pancreatic antibodies by a novel ELISA26citations
  • 2011Trial Protocol Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smoking3citations
  • 2005In vitro and in vivo analysis of macroporous biodegradable poly(D,L-lactide-co-glycolide) scaffolds containing bioactive glass100citations

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Chart of shared publication
Koutsoumpas, Andreas L.
1 / 1 shared
Shums, Zakera
1 / 1 shared
Pavlidis, Polychronis
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Smyk, Daniel S.
1 / 1 shared
Uemurea, Takeji
1 / 1 shared
Papp, Maria
1 / 1 shared
Milo, Jay
1 / 1 shared
Norman, Gary L.
1 / 1 shared
Bogdanos, Dimitrios P.
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Prevost, A. Toby
1 / 1 shared
Kinmonth, Ann Louise
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Watts, Sally
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Sanderson, Jeremy
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Hollands, Gareth J.
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Armstrong, David
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Whitwell, Sophia C. L.
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Mathew, Christopher G.
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Lewis, Cathryn M.
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Marteau, Theresa M.
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Sutton, Stephen
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Day, Richard M.
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Boccaccini, Aldo R.
1 / 77 shared
Jérôme, Robert
1 / 82 shared
Maquet, Véronique
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Chart of publication period
2015
2011
2005

Co-Authors (by relevance)

  • Koutsoumpas, Andreas L.
  • Shums, Zakera
  • Pavlidis, Polychronis
  • Smyk, Daniel S.
  • Uemurea, Takeji
  • Papp, Maria
  • Milo, Jay
  • Norman, Gary L.
  • Bogdanos, Dimitrios P.
  • Prevost, A. Toby
  • Kinmonth, Ann Louise
  • Watts, Sally
  • Sanderson, Jeremy
  • Hollands, Gareth J.
  • Armstrong, David
  • Whitwell, Sophia C. L.
  • Mathew, Christopher G.
  • Lewis, Cathryn M.
  • Marteau, Theresa M.
  • Sutton, Stephen
  • Day, Richard M.
  • Boccaccini, Aldo R.
  • Jérôme, Robert
  • Maquet, Véronique
OrganizationsLocationPeople

article

In vitro and in vivo analysis of macroporous biodegradable poly(D,L-lactide-co-glycolide) scaffolds containing bioactive glass

  • Day, Richard M.
  • Boccaccini, Aldo R.
  • Jérôme, Robert
  • Maquet, Véronique
  • Forbes, Alastair
Abstract

Recent studies have demonstrated the angiogenic potential of 45S5 Bioglass. However, it is not known whether the angiogenic properties of Bioglass remain when the bioactive glass particles are incorporated into polymer composites. The objectives of the current study were to investigate the angiogenic properties of 45S5 Bioglass particles incorporated into biodegradable polymer composites. In vitro studies demonstrated that fibroblasts cultured on discs consisting of specific quantities of Bioglass particles mixed into poly(D,L-lactide-co-glycolide) secreted significantly increased quantities of vascular endothelial growth factor. The optimal quantity of Bioglass particles determined from the in vitro experiments was incorporated into three-dimensional macroporous poly(D,L-lactide-co-glycolide) foam scaffolds. The foam scaffolds were fabricated using either compression molding or thermally induced phase separation processes. The foams were implanted subcutaneously into mice for periods of up to 6 weeks. Histological assessment was used to determine the area of granulation tissue around the foams, and the number of blood vessels within the granulation tissue was counted. The presence of Bioglass particles in the foams produced a sustained increase in the area of granulation tissue surrounding the foams. The number of blood vessels surrounding the neat foams was reduced after 2 weeks of implantation; however, compression-molded foams containing Bioglass after 4 and 6 weeks of implantation had significantly more blood vessels surrounding the foams compared with foams containing no Bioglass at the same time points. These results indicate that composite polymer foam scaffolds containing Bioglass particles retain granulation tissue and blood vessels surrounding the implanted foams. The use of this polymer composite for tissue engineering scaffolds might provide a novel approach for ensuring adequate vascular supply to the implanted device.

Topics
  • impedance spectroscopy
  • polymer
  • phase
  • experiment
  • glass
  • glass
  • composite
  • compression molding