2004
DOI: 10.1016/j.jacc.2004.04.040
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Injectable Fibrin Scaffold Improves Cell Transplant Survival, Reduces Infarct Expansion, and Induces Neovasculature Formation in Ischemic Myocardium

Abstract: This study indicates that fibrin glue increases cell transplant survival, decreases infarct size, and increases blood flow to ischemic myocardium. Therefore, fibrin glue may have potential as a biomaterial scaffold to improve cellular cardiomyoplasty treat and MIs.

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Cited by 496 publications
(410 citation statements)
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“…Christman et al pioneered the field of acellular injectable biomaterials by exploring the effects of fibrin glue as a bulking agent [18,23,34,48]. Fibrin has natural binding domains for soluble growth factors and cellular integrin receptors, motivating its use for wound healing applications.…”
Section: Natural Hydrogelsmentioning
confidence: 99%
See 3 more Smart Citations
“…Christman et al pioneered the field of acellular injectable biomaterials by exploring the effects of fibrin glue as a bulking agent [18,23,34,48]. Fibrin has natural binding domains for soluble growth factors and cellular integrin receptors, motivating its use for wound healing applications.…”
Section: Natural Hydrogelsmentioning
confidence: 99%
“…Fibrin has natural binding domains for soluble growth factors and cellular integrin receptors, motivating its use for wound healing applications. Although fibrin is commonly utilized for these biological properties, it can also be used as a mechanical support for the myocardium [18,29,34,48]. Specifically, fibrin forms a crosslinked 3-D hydrogel in the myocardium upon injection with a dual-barreled syringe.…”
Section: Natural Hydrogelsmentioning
confidence: 99%
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“…Our goal was to limit the variables associated with growth factor administration or immune rejection [Grinnemo et al, 2004] that may inhibit engraftment and confound interpretation of the results. PBSC or CD34þ cells purified by Isolex column, armed with MLCBi, and infused 24 h after a 17 min transient ligation of the LAD in nude rats led to remarkable numbers of armed and only a few unarmed cells present at 48 h in the infarct zone [Christman et al, 2004;Lum et al, 2004a]. No SC were seen in the non-infarcted areas of the rats.…”
mentioning
confidence: 99%