Vascular replacement using a layered elastin-collagen vascular graft in a porcine model: one week patency versus one month occlusion

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Publication year
2015Source
Organogenesis, 11, 3, (2015), pp. 105-21ISSN
Publication type
Article / Letter to editor

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Organization
Biochemistry (UMC)
Surgery
Central Animal Laboratory
Journal title
Organogenesis
Volume
vol. 11
Issue
iss. 3
Page start
p. 105
Page end
p. 21
Subject
Non Research Personnel Central Animal Laboratory are not attached to an institute / theme.; Radboudumc 10: Reconstructive and regenerative medicine RIHS: Radboud Institute for Health Sciences; Radboudumc 10: Reconstructive and regenerative medicine RIMLS: Radboud Institute for Molecular Life Sciences; NWP personeel van CDL vallen niet onder een instituut / themaAbstract
A persistent clinical demand exists for a suitable arterial prosthesis. In this study, a vascular conduit mimicking the native 3-layered artery, and constructed from the extracellular matrix proteins type I collagen and elastin, was evaluated for its performance as a blood vessel equivalent. A tubular 3-layered graft (elastin-collagen-collagen) was prepared using highly purified type I collagen fibrils and elastin fibers, resembling the 3-layered native blood vessel architecture. The vascular graft was crosslinked and heparinised (37 +/- 4 mug heparin/mg graft), and evaluated as a vascular graft using a porcine bilateral iliac artery model. An intra-animal comparison with clinically-used heparinised ePTFE (Propaten(R)) was made. Analyses included biochemical characterization, duplex scanning, (immuno)histochemistry and scanning electron microscopy. The tubular graft was easy to handle with adequate suturability. Implantation resulted in pulsating grafts without leakage. One week after implantation, both ePTFE and the natural acellular graft had 100% patencies on duplex scanning. Grafts were partially endothelialised (Von Willebrand-positive endothelium with a laminin-positive basal membrane layer). After one month, layered thrombi were found in the natural (4/4) and ePTFE graft (1/4), resulting in occlusion which in case of the natural graft is likely due to the porosity of the inner elastin layer. In vivo application of a molecularly-defined tubular graft, based on nature's matrix proteins, for vascular surgery is feasible.
This item appears in the following Collection(s)
- Academic publications [229134]
- Electronic publications [111496]
- Faculty of Medical Sciences [87758]
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