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)

  • 2015Surface Modification of Biodegradable Polymers towards Better Biocompatibility and Lower Thrombogenicity.36citations

Places of action

Chart of shared publication
Rudolph, A.
1 / 2 shared
Teske, Michael
1 / 18 shared
Sternberg, K.
1 / 1 shared
Wree, A.
1 / 1 shared
Hovakimyan, M.
1 / 1 shared
Grabow, N.
1 / 5 shared
Illner, S.
1 / 1 shared
Chart of publication period
2015

Co-Authors (by relevance)

  • Rudolph, A.
  • Teske, Michael
  • Sternberg, K.
  • Wree, A.
  • Hovakimyan, M.
  • Grabow, N.
  • Illner, S.
OrganizationsLocationPeople

article

Surface Modification of Biodegradable Polymers towards Better Biocompatibility and Lower Thrombogenicity.

  • Rudolph, A.
  • Teske, Michael
  • Sternberg, K.
  • Wree, A.
  • Hovakimyan, M.
  • Grabow, N.
  • Illner, S.
  • Kiefel, V.
Abstract

<h4>Purpose</h4>Drug-eluting stents (DES) based on permanent polymeric coating matrices have been introduced to overcome the in stent restenosis associated with bare metal stents (BMS). A further step was the development of DES with biodegradable polymeric coatings to address the risk of thrombosis associated with first-generation DES. In this study we evaluate the biocompatibility of biodegradable polymer materials for their potential use as coating matrices for DES or as materials for fully bioabsorbable vascular stents.<h4>Materials and methods</h4>Five different polymers, poly(L-lactide) PLLA, poly(D,L-lactide) PDLLA, poly(L-lactide-co-glycolide) P(LLA-co-GA), poly(D,L-lactide-co-glycolide) P(DLLA-co-GA) and poly(L-lactide-co-ε-caprolactone), P(LLA-co-CL) were examined in vitro without and with surface modification. The surface modification of polymers was performed by means of wet-chemical (NaOH and ethylenediamine (EDA)) and plasma-chemical (O2 and NH3) processes. The biocompatibility studies were performed on three different cell types: immortalized mouse fibroblasts (cell line L929), human coronary artery endothelial cells (HCAEC) and human umbilical vein endothelial cells (HUVEC). The biocompatibility was examined quantitatively using in vitro cytotoxicity assay. Cells were investigated immunocytochemically for expression of specific markers, and morphology was visualized using confocal laser scanning (CLSM) and scanning electron (SEM) microscopy. Additionally, polymer surfaces were examined for their thrombogenicity using an established hemocompatibility test.<h4>Results</h4>Both endothelial cell types exhibited poor viability and adhesion on all five unmodified polymer surfaces. The biocompatibility of the polymers could be influenced positively by surface modifications. In particular, a reproducible effect was observed for NH3-plasma treatment, which enhanced the cell viability, adhesion and morphology on all five polymeric surfaces.<h4>Conclusion</h4>Surface modification of polymers can provide a useful approach to enhance their biocompatibility. For clinical application, attempts should be made to stabilize the plasma modification and use it for coupling of biomolecules to accelerate the re-endothelialization of stent surfaces in vivo.

Topics
  • morphology
  • surface
  • polymer
  • scanning electron microscopy
  • biocompatibility
  • confocal laser scanning microscopy