2020
DOI: 10.3791/61824
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A Multi-Cue Bioreactor to Evaluate the Inflammatory and Regenerative Capacity of Biomaterials under Flow and Stretch

Abstract: DOI to the publisher's website.• The final author version and the galley proof are versions of the publication after peer review.• The final published version features the final layout of the paper including the volume, issue and page numbers. Link to publication General rightsCopyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal re… Show more

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Cited by 9 publications
(6 citation statements)
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“…The contractile balloon models underwent inflation–deflation cycles (of air) at a 60 beat per minute (BPM) rate (recapitulating that of the adult human heart [ 33 ] ) using a programmed bioreactor (Ibidi, USA). [ 34 ] For this purpose, the ATES was adhered to the collagen sheet (no glue), and then the assembly was glued to the surface of the silicon balloon. The whole system was immersed into deionized (DI) water.…”
Section: Methodsmentioning
confidence: 99%
“…The contractile balloon models underwent inflation–deflation cycles (of air) at a 60 beat per minute (BPM) rate (recapitulating that of the adult human heart [ 33 ] ) using a programmed bioreactor (Ibidi, USA). [ 34 ] For this purpose, the ATES was adhered to the collagen sheet (no glue), and then the assembly was glued to the surface of the silicon balloon. The whole system was immersed into deionized (DI) water.…”
Section: Methodsmentioning
confidence: 99%
“…Prior to cell seeding, culture medium was removed and 3.8*10 6 ODMCs/graft were seeded using fibrin as a cell carrier as described before. [ 31 ] In short, cells were suspended in a mixture of fibrinogen (bovine, 10 mg mL −1 , Sigma) and thrombin (bovine, 10 IU mL −1 , Sigma) and homogeneously dripped over both the lumen and adventitial side of the graft. To promote a uniform distribution of cells, the cell‐loaded constructs were rotated by 180° every 15 min in a general incubator (37 °C, 5% CO 2 ) for 1 h. After 1 h polymerization at 37 °C, SMGM2 medium with 0.25 mg mL −1 ascorbic acid was added to induce ECM production and ODMCs were further cultured in static conditions for 48 h.…”
Section: Methodsmentioning
confidence: 99%
“…For the 3D experiments, cells were seeded in electrospun PCL-BU scaffold, using fibrin as a cell carrier, as previously developed, 47 and as extensively described elsewhere. 48 Cells (monocultures: 30 • 10 6 macrophages/cm 3 or 15 • 10 6…”
Section: Cell Seeding In Scaffoldmentioning
confidence: 99%