The biocompatibility of a new material for cardiovascular applications constituted by a poly(ether)urethane (PEtU) and a silicone [polydimethylsiloxane (PDMS)] was evaluated. The achieved material shows properties similar to both polyurethanes and silicones. The material was transformed into porous membranes by a spray-deposition technique. Since any material preparation and manufacturing procedure may introduce some toxicity, in vitro cytotoxicity screening tests were carried out. Human umbilical vein endothelial cells (HUVECs) and a mouse fibroblasts cell line (L929) were cultivated with extracts obtained from materials containing 10, 40 and 100% (w/w) of PDMS. The commercially available Estane 5714-F1 and Cardiothane 51 were used as controls. Extracts were incubated up to 72 hours with HUVECs and L929 cells. The cytotoxic effect was evaluated by light microscopy, cell viability (MTT reduction and neutral red uptake) and proliferation (5-bromo-2'-deoxyuridine incorporation) tests. In vivo studies were carried out using materials containing the same PDMS percentages as for in vitro experiments. The same commercial controls were used. Results obtained with cell culture studies agreed with those obtained in the in vivo experiments and showed that the material preparation and manufacturing procedure do not introduce any toxicity in the products at each PDMS concentration investigated.

SummaryIn small-diameter vascular grafts, the porosity of the internal surface plays an important role because it affects initial thrombus deposition and therefore the graft's patency. As well as many other studies reported in the literature we have carried out a study of the relationship between porosity and the manufacturing parameters of polyurethane (PU) grafts by standard scanning electron microscopy (SEM) analysis. However, SEM was not completely satisfactory for evaluating the 'sponge-like' uptake of water by the graft due to the unavoidable water loss and metal coating during preparation. In fact this preparation produces artefacts of the three-dimensional porous structure. To avoid this problem we investigated the possibility of observing the graft's internal surface through a stereomicroscope after it had absorbed water. We looked into a simple staining procedure which preferentially colours the PU graft fibres with respect to the void areas. After testing different kinds of stains, we eventually found that Sudan Black B, which usually stains for all kinds of lipid, turned out to be an excellent stain for the water-loaded PU grafts when diluted with ethanol. This staining procedure, coupled with a computerized image analysis system, allowed us to evaluate the degree of void and average void size of the graft internal surface and to correlate these data with graft density and manufacturing parameters.

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The hydrophobicity of metal–organic frameworks (MOFs) is critical in enhancing the separation process in membrane distillation. Herein, a new superhydrophobic University of Oslo 66 (UiO-66) MOFs was successfully constructed on the top of alumina hollow fibre (AHF) membrane for desalination purposes. The fabrication methodology of the membrane involved in situ growth of pure crystalline UiO-66 on top of AHF and post-synthetic modification by fluorosilane grafting. The resultant membrane was characterised to study the physicochemical properties of the pristine and modified membrane. A superhydrophobic UiO-66 with a contact angle of 163.6° and high liquid entry pressure was obtained by introducing a highly branched fluorocarbon chain while maintaining its crystallinity. As a result, the modified membrane achieved 14.95 L/m2∙h water flux and 99.9% NaCl rejection with low energy consumption in the direct contact membrane distillation process. Furthermore, the high surface energy contributed by UiO-66 is maximised to produce the maximum number of accessible sites for the grafting process. The synergistic effect of surface hydrophobicity and porous UiO-66 membrane in trapping water vapour shows great potential for desalination application.