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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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)

  • 2023A tissue engineered 3D printed calcium alkali phosphate bioceramic bone graft enables vascularization and regeneration of critical-size discontinuity bony defects in vivo.14citations

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Berger, G.
1 / 4 shared
Stiller, M.
1 / 4 shared
Koerdt, S.
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Rendenbach, C.
1 / 8 shared
Houshmand, A.
1 / 4 shared
Heiland, Max
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Steffen, C.
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Xiang-Tischhauser, L.
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Adel-Khattab, D.
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Knabe, C.
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Günster, J.
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Gildenhaar, R.
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Peleska, B.
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Kampschulte, M.
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Rack, A.
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Linow, U.
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2023

Co-Authors (by relevance)

  • Berger, G.
  • Stiller, M.
  • Koerdt, S.
  • Rendenbach, C.
  • Houshmand, A.
  • Heiland, Max
  • Steffen, C.
  • Xiang-Tischhauser, L.
  • Adel-Khattab, D.
  • Knabe, C.
  • Günster, J.
  • Gildenhaar, R.
  • Peleska, B.
  • Kampschulte, M.
  • Rack, A.
  • Linow, U.
OrganizationsLocationPeople

article

A tissue engineered 3D printed calcium alkali phosphate bioceramic bone graft enables vascularization and regeneration of critical-size discontinuity bony defects in vivo.

  • Wilbig, J.
  • Berger, G.
  • Stiller, M.
  • Koerdt, S.
  • Rendenbach, C.
  • Houshmand, A.
  • Heiland, Max
  • Steffen, C.
  • Xiang-Tischhauser, L.
  • Adel-Khattab, D.
  • Knabe, C.
  • Günster, J.
  • Gildenhaar, R.
  • Peleska, B.
  • Kampschulte, M.
  • Rack, A.
  • Linow, U.
Abstract

Introduction: Recently, efforts towards the development of patient-specific 3D printed scaffolds for bone tissue engineering from bioactive ceramics have continuously intensified. For reconstruction of segmental defects after subtotal mandibulectomy a suitable tissue engineered bioceramic bone graft needs to be endowed with homogenously distributed osteoblasts in order to mimic the advantageous features of vascularized autologous fibula grafts, which represent the standard of care, contain osteogenic cells and are transplanted with the respective blood vessel. Consequently, inducing vascularization early on is pivotal for bone tissue engineering. The current study explored an advanced bone tissue engineering approach combining an advanced 3D printing technique for bioactive resorbable ceramic scaffolds with a perfusion cell culture technique for pre-colonization with mesenchymal stem cells, and with an intrinsic angiogenesis technique for regenerating critical size, segmental discontinuity defects in vivo applying a rat model. To this end, the effect of differing Si-CAOP (silica containing calcium alkali orthophosphate) scaffold microarchitecture arising from 3D powder bed printing (RP) or the Schwarzwalder Somers (SSM) replica fabrication technique on vascularization and bone regeneration was analyzed in vivo. In 80 rats 6-mm segmental discontinuity defects were created in the left femur. Methods: Embryonic mesenchymal stem cells were cultured on RP and SSM scaffolds for 7d under perfusion to create Si-CAOP grafts with terminally differentiated osteoblasts and mineralizing bone matrix. These scaffolds were implanted into the segmental defects in combination with an arteriovenous bundle (AVB). Native scaffolds without cells or AVB served as controls. After 3 and 6 months, femurs were processed for angio-µCT or hard tissue histology, histomorphometric and immunohistochemical analysis of angiogenic and osteogenic marker expression. Results: At 3 and 6 months, defects reconstructed with RP scaffolds, cells and AVB displayed a statistically significant higher bone area fraction, blood vessel volume%, blood vessel surface/volume, blood vessel thickness, density and linear density than defects treated with the other scaffold configurations. Discussion: Taken together, this study demonstrated that the AVB technique is well suited for inducing adequate vascularization of the tissue engineered scaffold graft in segmental defects after 3 and 6 months, and that our tissue engineering approach employing 3D powder bed printed scaffolds facilitated segmental defect repair.

Topics
  • density
  • impedance spectroscopy
  • surface
  • defect
  • ceramic
  • Calcium