In Vitro and in Vivo Biodurability of a Compliant Microporous Vascular Graft

1998 ◽  
Vol 13 (1) ◽  
pp. 23-45 ◽  
Author(s):  
A. Edwards ◽  
R. J. Carson ◽  
M. Szycher ◽  
S. Bowald
Keyword(s):  
2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Edward X. Han ◽  
Hong Qian ◽  
Bo Jiang ◽  
Maria Figetakis ◽  
Natalia Kosyakova ◽  
...  

AbstractA significant barrier to implementation of cell-based therapies is providing adequate vascularization to provide oxygen and nutrients. Here we describe an approach for cell transplantation termed the Therapeutic Vascular Conduit (TVC), which uses an acellular vessel as a scaffold for a hydrogel sheath containing cells designed to secrete a therapeutic protein. The TVC can be directly anastomosed as a vascular graft. Modeling supports the concept that the TVC allows oxygenated blood to flow in close proximity to the transplanted cells to prevent hypoxia. As a proof-of-principle study, we used erythropoietin (EPO) as a model therapeutic protein. If implanted as an arteriovenous vascular graft, such a construct could serve a dual role as an EPO delivery platform and hemodialysis access for patients with end-stage renal disease. When implanted into nude rats, TVCs containing EPO-secreting fibroblasts were able to increase serum EPO and hemoglobin levels for up to 4 weeks. However, constitutive EPO expression resulted in macrophage infiltration and luminal obstruction of the TVC, thus limiting longer-term efficacy. Follow-up in vitro studies support the hypothesis that EPO also functions to recruit macrophages. The TVC is a promising approach to cell-based therapeutic delivery that has the potential to overcome the oxygenation barrier to large-scale cellular implantation and could thus be used for a myriad of clinical disorders. However, a complete understanding of the biological effects of the selected therapeutic is absolutely essential.


2016 ◽  
Vol 44 (11) ◽  
pp. 3319-3334 ◽  
Author(s):  
Marjan Enayati ◽  
Magdalena Eilenberg ◽  
Christian Grasl ◽  
Peter Riedl ◽  
Christoph Kaun ◽  
...  
Keyword(s):  

2020 ◽  
Vol 48 ◽  
pp. 55
Author(s):  
Alberto Maria Settembrini ◽  
Antonio Alessandrino ◽  
Anna Chiarini ◽  
Giuliano Freddi ◽  
Ilaria Dal Prà ◽  
...  

1999 ◽  
Author(s):  
Diane L. Hern-Anderson ◽  
Anne Marie J. Hernandez ◽  
John P. Ranieri ◽  
Steven Weinberg

Abstract Many have hypothesized that both chemical and mechanical material properties are important in the design of a small bore vascular graft. In an attempt to address both issues, a xenogeneic graft crosslinked by photo-oxidation and covalently modified with heparin was developed. The compliance, burst strength, and suture pull strength of photo-oxidized (PhotoFix®) and heparin-modified photo-oxidized ovine carotid tissue were tested in vitro. The heparin modification process was found to have no statistically significant effect on any of these properties. The shrink temperature of fresh, photo-oxidized, and heparin-modified photo-oxidized tissue was assessed using DSC. A small increase in the shrink temperature of the heparin-modified photo-oxidized tissue over the fresh tissue was found to be statistically significant (P < 0.05). In vivo assessment of unmodified, heparin-soaked, and heparin-modified PhotoFix ovine grafts indicated that covalent modification of the grafts was imperative for the graft’s success.


2012 ◽  
Vol 46 (3) ◽  
pp. 212-222 ◽  
Author(s):  
Mark Tatterton ◽  
Stacy-Paul Wilshaw ◽  
Eileen Ingham ◽  
Shervanthi Homer-Vanniasinkam

Background. Thrombosis of synthetic small-diameter bypass grafts remains a major problem. The aim of this article is to review the antithrombotic strategies that have been used in an attempt to reduce graft thrombogenicity. Methods. A PubMed/MEDLINE search was performed using the search terms “vascular graft thrombosis,” “small-diameter graft thrombosis,” “synthetic graft thrombosis” combined with “antithrombotic,” “antiplatelet,” “anticoagulant,” “Dacron,” “PTFE,” and “polyurethane.” Results. The majority of studies on antithrombotic therapies have used either in vitro models or in vivo animal experiments. Many of the therapies used in these settings do show antithrombotic efficacy against synthetic graft materials. There is however, a distinct lack of human in vivo studies to further delineate the performance and limitations of therapies displaying good antithrombotic characteristics. Conclusion. Very few antithrombotic therapies have translated into clinical use. More human in vivo studies are required to assess the efficacy and safety of such therapies.


2017 ◽  
Vol 44 ◽  
pp. 244-249 ◽  
Author(s):  
Yun-Tao Hu ◽  
Xu-Dong Pan ◽  
Jun Zheng ◽  
Wei-Guo Ma ◽  
Li-Zhong Sun

2017 ◽  
Vol 12 (6) ◽  
pp. 065003 ◽  
Author(s):  
A Aussel ◽  
N B Thébaud ◽  
X Bérard ◽  
V Brizzi ◽  
S Delmond ◽  
...  

2019 ◽  
Vol 69 (6) ◽  
pp. e84
Author(s):  
Alberto Settembrini ◽  
Antonio Alessandrino ◽  
Anna Chiarini ◽  
Giuliano Freddi ◽  
Ilaria Dal Pra ◽  
...  

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