2023
DOI: 10.1016/j.bioadv.2023.213328
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Hemocompatibility tuning of an innovative glutaraldehyde-free preparation strategy using riboflavin/UV crosslinking and electron irradiation of bovine pericardium for cardiac substitutes

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Cited by 2 publications
(3 citation statements)
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“…35 As the SULEEI procedure is a novel GA-free strategy to produce xenogenic pericardial material for biological aortic valve (AV) prostheses and patch material, 28 this is the first report about the cellular response after implantation of SULEEI-pericardium into a living vertebrate. As recently shown, the SULEEI protocol incorporates efficient decellularization, resulting in the elimination of α-Gal epitopes and DNA fragments to less than 300 bp, 30 which is reported to be nonimmunogenic. 36 Our results demonstrate that SULEEI-pericardium evokes a similar immune reaction and tissue response as the clinically used control standard bovine patch material.…”
Section: A Cellular and Tissue Responsementioning
confidence: 99%
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“…35 As the SULEEI procedure is a novel GA-free strategy to produce xenogenic pericardial material for biological aortic valve (AV) prostheses and patch material, 28 this is the first report about the cellular response after implantation of SULEEI-pericardium into a living vertebrate. As recently shown, the SULEEI protocol incorporates efficient decellularization, resulting in the elimination of α-Gal epitopes and DNA fragments to less than 300 bp, 30 which is reported to be nonimmunogenic. 36 Our results demonstrate that SULEEI-pericardium evokes a similar immune reaction and tissue response as the clinically used control standard bovine patch material.…”
Section: A Cellular and Tissue Responsementioning
confidence: 99%
“…28 This protocol, developed for porcine tissue, was adapted for thicker bovine tissue. [29][30][31] Pericardial tissue was stored in 5 mM Tris(hydroxymethyl)aminomethane (Tris, pH = 8) for 60 h, containing 2% phenoxyethanol to inhibit bacterial growth. Within the first sterilization step, tissue was incubated in 1% Triton X-100 in 5 mM Tris (pH = 8) at 4 ○ C for 8 h, followed by DNAse (0.1 mg/ml), RNAse (0.02 mg/ml), and trypsin (0.004 μg/ml) in HBSS at 37 ○ C for 15 h. Subsequently, again, an incubation in 1% Triton X-100 in 5 mM Tris (pH = 8) at 4 ○ C for 7 h took place.…”
Section: Experimental a Preparation Of Pericardial Implantsmentioning
confidence: 99%
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