Paul Barham
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Paul Barham has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Christian R. Wilhelmsen
Nofima AS, Pb 210, NO-1431 Ås, Norway
1 shared publication - Eirik Haugen
Nofima AS, Pb 210, NO-1431 Ås, Norway
1 shared publication - Eva Veiseth-Kent
Nofima AS, Osloveien 1, 1430 Ås, Norway
1 shared publication - Henri-Pierre Suso
Biovotec AS, Postbox 1001 Hoff, 0218 Oslo, Norway
1 shared publication - Mona Elisabeth Pedersen
Nofima AS, Osloveien 1, 1433 Ås, Norway
1 shared publication - Ragnhild S. Berg
Nofima AS, Pb 210, NO-1431 Ås, Norway
1 shared publication
Latest Publications
- Open Access
- 30 October 2020
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 21 (21) , 8130
Processed Eggshell Membrane Powder Is a Promising Biomaterial for Use in Tissue Engineering
The purpose of this study was to investigate the tissue regenerating and biomechanical properties of processed eggshell membrane powder (PEP) for use in 3D-scaffolds. PEP is a low-cost, natural biomaterial with beneficial bioactive properties. Most importantly, this material is available as a by-product of the chicken egg processing (breaking) industry on a large scale, and it could have potential as a low-cost ingredient for therapeutic scaffolds. Scaffolds consisting of collagen alone and collagen combined with PEP were produced and analyzed for their mechanical properties and the growth of primary fibroblasts and skeletal muscle cells. Mechanical testing revealed that a PEP/collagen-based scaffold increased the mechanical hardness of the scaffold compared with a pure collagen scaffold. Scanning electron microscopy (SEM) demonstrated an interconnected porous structure for both scaffolds, and that the PEP was evenly distributed in dense clusters within the scaffold. Fibroblast and skeletal muscle cells attached, were viable and able to proliferate for 1 and 2 weeks in both scaffolds. The cell types retained their phenotypic properties expressing phenotype markers of fibroblasts (TE7, alpha-smooth muscle actin) and skeletal muscle (CD56) visualized by immunostaining. mRNA expression of the skeletal muscle markers myoD, myogenin, and fibroblasts marker (SMA) together with extracellular matrix components supported viable phenotypes and matrix-producing cells in both types of scaffolds. In conclusion, PEP is a promising low-cost, natural biomaterial for use in combination with collagen as a scaffold for 3D-tissue engineering to improve the mechanical properties and promote cellular adhesion and growth of regenerating cells.
- 30 October 2020
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 21 (21) , 8130
Open AccessProcessed Eggshell Membrane Powder Is a Promising Biomaterial for Use in Tissue Engineering
The purpose of this study was to investigate the tissue regenerating and biomechanical properties of processed eggshell membrane powder (PEP) for use in 3D-scaffolds. PEP is a low-cost, natural biomaterial with beneficial bioactive properties. Most importantly, this material is available as a by-product of the chicken egg processing (breaking) industry on a large scale, and it could have potential as a low-cost ingredient for therapeutic scaffolds. Scaffolds consisting of collagen alone and collagen combined with PEP were produced and analyzed for their mechanical properties and the growth of primary fibroblasts and skeletal muscle cells. Mechanical testing revealed that a PEP/collagen-based scaffold increased the mechanical hardness of the scaffold compared with a pure collagen scaffold. Scanning electron microscopy (SEM) demonstrated an interconnected porous structure for both scaffolds, and that the PEP was evenly distributed in dense clusters within the scaffold. Fibroblast and skeletal muscle cells attached, were viable and able to proliferate for 1 and 2 weeks in both scaffolds. The cell types retained their phenotypic properties expressing phenotype markers of fibroblasts (TE7, alpha-smooth muscle actin) and skeletal muscle (CD56) visualized by immunostaining. mRNA expression of the skeletal muscle markers myoD, myogenin, and fibroblasts marker (SMA) together with extracellular matrix components supported viable phenotypes and matrix-producing cells in both types of scaffolds. In conclusion, PEP is a promising low-cost, natural biomaterial for use in combination with collagen as a scaffold for 3D-tissue engineering to improve the mechanical properties and promote cellular adhesion and growth of regenerating cells.