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)

  • 2011Micropatterning of bioactive heparin-based hydrogels33citations

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Revzin, Alexander
1 / 2 shared
Tae, Giyoong
1 / 5 shared
Shah, Sunny Satish
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Kim, Mihye
1 / 2 shared
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2011

Co-Authors (by relevance)

  • Revzin, Alexander
  • Tae, Giyoong
  • Shah, Sunny Satish
  • Kim, Mihye
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article

Micropatterning of bioactive heparin-based hydrogels

  • Revzin, Alexander
  • Tae, Giyoong
  • Shah, Sunny Satish
  • Cahill-Thompson, Katelyn
  • Kim, Mihye
Abstract

This paper describes a UV photopatterning of bioactive heparin-based hydrogels on glass substrates. In this approach, hydrogel micropatterns were formed by UV-initiated thiol-ene reaction between thiolated heparin and diacrylated poly(ethylene) glycol (PEG-DA). Analysis of gelation kinetics showed that photo-crosslinked hydrogels formed faster and were stronger when compared to hydrogels formed by competing Michael addition reaction. To highlight bioactivity of heparin-PEG hybrid gels, hepatocyte growth factor (HGF) was mixed into prepolymer solution prior to hydrogel patterning. Immunostaining showed that HGF was retained after 5 days in the hybrid heparin-PEG hydrogel microstructures but was rapidly released from pure PEG gel microstructures. In a set of experiments further highlighting bioactivity of microfabricated heparin-based hydrogel, primary rat hepatocytes were cultured next to heparin and pure PEG hydrogel disks (similar to 500 mu m in diameter). ELISA analysis revealed that hepatocytes residing next to heparin-based hydrogels were producing similar to 4 times more albumin at day 7 compared to cells cultured next to inert PEG hydrogels. In the future, microfabricated heparin-based hydrogels described in this paper will be employed for designing cellular microenvironment in vitro and as vehicles for cell transplantation in vivo.

Topics
  • microstructure
  • experiment
  • glass
  • glass
  • gelation
  • bioactivity