Covalent RGD Modification of the Inner Pore Surface of Polycaprolactone Scaffolds-Reference-Cited by-同舟云学术

Covalent RGD Modification of the Inner Pore Surface of Polycaprolactone Scaffolds

Published:2012-01-01 Issue:7 Volume:23 Page:941-953
ISSN:0920-5063
Container-title:Journal of Biomaterials Science, Polymer Edition
language:en
Short-container-title:Journal of Biomaterials Science, Polymer Edition

Author:

Gabriel Matthias¹,Nazmi Kamran²,Dahm Manfred³,Zentner Andrej⁴,Vahl Christian-Friedrich⁵,Strand Dennis⁶

Affiliation:

1. a Department of Cardiothoracic and Vascular Surgery, Johannes Gutenberg-University School of Medicine, Langenbeckstr. 1, B 505, 55131 Mainz, Germany. mgabriel@uni-mainz.de

2. b Academic Centre for Dentistry Amsterdam (ACTA), Louwesweg 1, 1066 EA Amsterdam, The Netherlands

3. c Department of Cardiothoracic and Vascular Surgery, Johannes Gutenberg-University School of Medicine, Langenbeckstr. 1, B 505, 55131 Mainz, Germany

4. d Academic Centre for Dentistry Amsterdam (ACTA), Louwesweg 1, 1066 EA Amsterdam, The Netherlands

5. e Department of Cardiothoracic and Vascular Surgery, Johannes Gutenberg-University School of Medicine, Langenbeckstr. 1, B 505, 55131 Mainz, Germany

6. f First Department of Internal Medicine, Johannes Gutenberg-University School of Medicine, Obere Zahlbacher Str. 63, 55131 Mainz, Germany

Publisher

Informa UK Limited

Subject

Biomedical Engineering,Biomaterials,Bioengineering,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1163/092050611X566793

Reference12 articles.

1. Cell colonization in degradable 3D porous matrices

2. Polymeric Scaffolds for Bone Tissue Engineering

3. Controllable Surface Modification of Poly(lactic-co-glycolic acid) (PLGA) by Hydrolysis or Aminolysis I: Physical, Chemical, and Theoretical Aspects

4. Surface Modification of Polycaprolactone Membrane via Aminolysis and Biomacromolecule Immobilization for Promoting Cytocompatibility of Human Endothelial Cells

5. Peptide-surface modification of poly(caprolactone) with laminin-derived sequences for adipose-derived stem cell applications

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