4.8 Article

A bilayered elastomeric scaffold for tissue engineering of small diameter vascular grafts

期刊

ACTA BIOMATERIALIA
卷 6, 期 1, 页码 110-122

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2009.06.026

关键词

Vascular tissue engineering; Tubular scaffold; Polymer processing; Cellseeding; Poly(ester urethane)urea

资金

  1. US National Institutes of Health [R01 HL069368]
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL069368] Funding Source: NIH RePORTER

向作者/读者索取更多资源

A major barrier to the development of a clinically useful small diameter tissue engineered vascular graft (TEVG) is the scaffold component. Scaffold requirements include matching the mechanical and structural properties with those of native vessels and optimizing the microenvironment to foster cell integration, adhesion and growth. We have developed a small diameter, bilayered, biodegradable, elastomeric scaffold based on a synthetic, biodegradable elastomer. The scaffold incorporates a highly porous inner layer, allowing cell integration and growth, and an external, fibrous reinforcing layer deposited by electrospinning. Scaffold morphology and mechanical properties were assessed, quantified and compared with those of native vessels. Scaffolds were then seeded with adult stem cells using a rotational vacuum seeding device to obtain a TEVG, cultured under dynamic conditions for 7 days and evaluated for cellularity. The scaffold showed firm integration of the two polymeric layers with no delamination. Mechanical properties were physiologically consistent, showing anisotropy, an elastic modulus (1.4 +/- 0.4 MPa) and an ultimate tensile stress (8.3 +/- 1.7 MPa) comparable with native vessels. The compliance and suture retention forces were 4.6 +/- 0.5 x 10(-4) mmHg(-1) and 3.4 +/- 0.3 N, respectively. Seeding resulted in a rapid, uniform, bulk integration of cells, with a seeding efficiency of 92 +/- 1%. The scaffolds maintained a high level of cellular density throughout dynamic culture. This approach, combining artery-like mechanical properties and a rapid and efficient cellularization, might contribute to the future clinical translation of TEVGs. (C) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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