TY - JOUR
T1 - Preparation and characterization of a scaffold for vascular tissue engineering by direct-assembling of collagen and cells in a cylindrical geometry
AU - Boccafoschi, Francesca
AU - Rajan, Navneeta
AU - Habermehl, Jason
AU - Mantovani, Diego
PY - 2007/5/10
Y1 - 2007/5/10
N2 - In the past 25 years, several efforts have been focused on developing vascular substitutes showing long-term patency when implanted in humans. In this study, we present our last findings in an ongoing project aiming to develop a tissue-regenerated blood vessel from collagen-based scaffolds. A collagen-based scaffold with adequate biological properties was developed by directly assembling collagen and cells in a cylindrical geometry. The technique mainly involves the use of a ventilated rotating tube allowing smooth muscle cells to grow in a cylindrical collagen matrix. Scanning electron microscopy (SEM), histology, and cell cycle analyses were carried out in order to assess the biological potential of the cell-based scaffold for further maturation. Compliance results showed that this technique allows cells to assemble in the collagen matrix, thus providing enough rigidity to the structure to be handled and mounted in a perfusion bioreactor for further growth and maturation. (Figure Presented)
AB - In the past 25 years, several efforts have been focused on developing vascular substitutes showing long-term patency when implanted in humans. In this study, we present our last findings in an ongoing project aiming to develop a tissue-regenerated blood vessel from collagen-based scaffolds. A collagen-based scaffold with adequate biological properties was developed by directly assembling collagen and cells in a cylindrical geometry. The technique mainly involves the use of a ventilated rotating tube allowing smooth muscle cells to grow in a cylindrical collagen matrix. Scanning electron microscopy (SEM), histology, and cell cycle analyses were carried out in order to assess the biological potential of the cell-based scaffold for further maturation. Compliance results showed that this technique allows cells to assemble in the collagen matrix, thus providing enough rigidity to the structure to be handled and mounted in a perfusion bioreactor for further growth and maturation. (Figure Presented)
KW - Biological and hematological performances
KW - Collagen
KW - Compliance
KW - Cylindrical scaffolds
KW - Growth
KW - Mechanical properties
KW - Synthesis
KW - Vascular cells
KW - Vascular tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=34547947952&partnerID=8YFLogxK
U2 - 10.1002/mabi.200600242
DO - 10.1002/mabi.200600242
M3 - Article
SN - 1616-5187
VL - 7
SP - 719
EP - 726
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 5
ER -