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End date: 2024 × Start date: 2020 × DDC: 500 × Type: article × search.filters.applied.f.series: Scientific reports 8 (2018) × WGL Institute: DWI ×

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    Engineering biofunctional in vitro vessel models using a multilayer bioprinting technique
    ([London] : Macmillan Publishers Limited, part of Springer Nature, 2018) Schöneberg, Jan; De Lorenzi, Federica; Theek, Benjamin; Blaeser, Andreas; Rommel, Dirk; Kuehne, Alexander J. C.; Kießling, Fabian; Fischer, Horst
    Recent advances in the field of bioprinting have led to the development of perfusable complex structures. However, most of the existing printed vascular channels lack the composition or key structural and physiological features of natural blood vessels or they make use of more easily printable but less biocompatible hydrogels. Here, we use a drop-on-demand bioprinting technique to generate in vitro blood vessel models, consisting of a continuous endothelium imitating the tunica intima, an elastic smooth muscle cell layer mimicking the tunica media, and a surrounding fibrous and collagenous matrix of fibroblasts mimicking the tunica adventitia. These vessel models with a wall thickness of up to 425 µm and a diameter of about 1 mm were dynamically cultivated in fluidic bioreactors for up to three weeks under physiological flow conditions. High cell viability (>83%) after printing and the expression of VE-Cadherin, smooth muscle actin, and collagen IV were observed throughout the cultivation period. It can be concluded that the proposed novel technique is suitable to achieve perfusable vessel models with a biofunctional multilayer wall composition. Such structures hold potential for the creation of more physiologically relevant in vitro disease models suitable especially as platforms for the pre-screening of drugs.
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    Microfluidic cell sorting: Towards improved biocompatibility of extracorporeal lung assist devices
    ([London] : Macmillan Publishers Limited, part of Springer Nature, 2018) Bleilevens, Christian; Lölsberg, Jonas; Cinar, Arne; Knoben, Maren; Grottke, Oliver; Rossaint, Rolf; Wessling, Matthias
    Extracorporeal lung assist technology is one of the last options in critical care medicine to treat patients suffering from severe oxygenation and decarboxylation disorders. Platelet activation along with the consequent thrombus formation is a potentially life-threatening complication of this technique. To avoid platelet-dependent clot formation, this study aims at developing a microfluidic cell sorting chip that can bypass platelets prior to the membrane oxygenator of the extracorporeal lung assist device. The cell sorting chips were produced by maskless dip-in laser lithography, followed by soft lithography replication using PDMS. Citrated porcine whole blood with a clinically relevant haematocrit of 17% was used for the cell sorting experiments involving three different blood flow rates. The joint effects of flow focusing and hydrodynamic lifting forces within the cell sorting chip resulted in a reduction of up to 57% of the baseline platelet count. This cell sorting strategy is suitable for the continuous and label-free separation of red blood cells and platelets and is potentially applicable for increasing the biocompatibility and lifetime of current extracorporeal lung assist devices.