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 (1/1 displayed)

  • 2021Surface Modification of Bioactive Glass Promotes Cell Attachment and Spreading18citations

Places of action

Chart of shared publication
Huynh, Ngoc
1 / 3 shared
Azizi, Latifeh
1 / 3 shared
Massera, Jonathan M.
1 / 1 shared
Hytönen, Vesa P.
1 / 2 shared
Chart of publication period
2021

Co-Authors (by relevance)

  • Huynh, Ngoc
  • Azizi, Latifeh
  • Massera, Jonathan M.
  • Hytönen, Vesa P.
OrganizationsLocationPeople

article

Surface Modification of Bioactive Glass Promotes Cell Attachment and Spreading

  • Huynh, Ngoc
  • Turkki, Paula
  • Azizi, Latifeh
  • Massera, Jonathan M.
  • Hytönen, Vesa P.
Abstract

Phosphate glasses have several advantages over traditional silicate-based bioglasses but are inferior in the crucial step of cell attachment to their surface. Here, as a proof of concept, we analyze fibroblast attachment to the phosphate glass surface subjected to basic treatment and silanization. Silicate (S53P4)- and phosphate (Sr50)-based bioactive glasses were either untreated or surface-treated with basic buffer and functionalized with silane. The surface-treated samples were studied as such and after fibronectin was adsorbed on to their surface. With both glass types, surface treatment enhanced fibroblast adhesion and spreading in comparison to the untreated glass. The surface-treated Sr50 glass allowed for cell adhesion, proliferation, and spreading to a similar extent as seen with S53P4 and borosilicate control glasses. Here, we show that surface treatment of bioactive glass can be used to attract cell adhesion factors found in the serum and promote cell–material adhesion, both important for efficient tissue integration. ; Peer reviewed

Topics
  • surface
  • glass
  • glass