1999
DOI: 10.1007/s100169900232
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In Vitro Endothelialization of PTFE Vascular Grafts: A Comparison of Various Substrates, Cell Densities, and Incubation Times

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Cited by 22 publications
(15 citation statements)
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“…These observations could explain the differences of results between these two supports, which have different physical and chemical properties. Fibronectin is a biological material, which presents some limits (as indicated in the introduction section) and risks, since extracted from blood, of the transmission of virus 51. The build‐up on the vascular graft luminal surface with such PMF has the main advantages to be easily realized (by simple alternated polyelectrolyte solution flowing) and finally induce only a minimal reduction of the cross‐section (film with few tens of nanometers thickness).…”
Section: Resultsmentioning
confidence: 99%
“…These observations could explain the differences of results between these two supports, which have different physical and chemical properties. Fibronectin is a biological material, which presents some limits (as indicated in the introduction section) and risks, since extracted from blood, of the transmission of virus 51. The build‐up on the vascular graft luminal surface with such PMF has the main advantages to be easily realized (by simple alternated polyelectrolyte solution flowing) and finally induce only a minimal reduction of the cross‐section (film with few tens of nanometers thickness).…”
Section: Resultsmentioning
confidence: 99%
“…To improve their long-term biocompatibility and hemocompatibility, it is necessary to recreate an internal environment similar to that found in native vessels. [6][7][8][9] For such an objective, EC seeding and tissue engineering techniques have been previously developed. 10 However, EC seeding on ePTFE has limited success due to the existence of electrostatic repulsive interactions between the negatively charged ECs and the negatively charged graft material.…”
Section: Introductionmentioning
confidence: 99%
“…Unfortunately, synthetic small diameter vascular grafts have unacceptable patency rates primarily due to lumenal thrombus formation and intimal thickening [3]. Lumenal endothelialization represents a clear, immediate, and practical solution to poor graft patency [4]. However, the promise of this approach has not been realized because of numerous unresolved issues concerning seeding efficiency, cell retention under flow, and achieving a quiescent and anti-thrombotic endothelial cell (EC) phenotype that resists thrombosis, intimal hyperplasia, and leukocyte adhesion [5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%