Small diameter vascular graft with fibroblast cells and electrospun poly (L-lactide-co-epsilon-caprolactone) scaffolds: Cell Matrix Engineering

Authors
Jang, Bong SeokCheon, Ja YoungKim, Soo HyunPark, Won Ho
Issue Date
2018-03
Publisher
TAYLOR & FRANCIS LTD
Citation
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, v.29, no.7-9, pp.942 - 959
Abstract
Electrospun scaffolds have been widely used in tissue engineering due to their similar structure to native extracellular matrices (ECM). However, one of the obstacles limiting the application of electrospun scaffolds for tissue engineering is the nano-sized pores, which inhibit cell infiltration into the scaffolds. To overcome this limitation, we approached to make layers which are consisted of cells onto the electrospun sheet and then tubular structure was constructed by rolling. We called this as Cell Matrix Engineering' because the electrospun sheets were combined with the cells to form one matrix. They maintained 3-D tubular structures well and their diameters were 4.1mm (+/- 0.1mm). We compared the mechanical and biological properties of various vascular grafts with the electrospun PLCL sheets of different thickness. In these experiments, the vascular graft made with thin sheets showed a better cell proliferation and attachment than the grafts made with thick sheets because the thin layer allowed for more efficient mass transfer and better permeability than the thick layer. Culturing under physiological pulsatile flow condition was demonstrated in this work. These dynamic conditions provided the improved mass transport and aerobic cell metabolism. Therefore, the Cell Matrix Engineered vascular graft holds a great promise for clinical applications by overcoming the limitations associated with conventional scaffolds.
Keywords
MESENCHYMAL STEM-CELLS; IN-VITRO; DEGRADATION BEHAVIOR; TISSUE; POLY(L-LACTIDE-CO-EPSILON-CAPROLACTONE); NANOFIBER; FABRICATION; INFILTRATION; COLLAGEN; DESIGN; Vascular graft; fibroblast cells; electrospun poly(L-lactide-co-epsilon-caprolactone); Cell Matrix Engineering
ISSN
0920-5063
URI
https://pubs.kist.re.kr/handle/201004/121639
DOI
10.1080/09205063.2017.1367635
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KIST Article > 2018
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