tecoflex has been researched along with Hemolysis* in 2 studies
2 other study(ies) available for tecoflex and Hemolysis
Article | Year |
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In vitro thrombogenicity investigation of new water-dispersible polyurethane anionomers bearing carboxylate groups.
New segmented polyurethane (PU) anionomers based on hydroxytelechelic polybutadiene were synthesized via an aqueous dispersion process. Incorporation of carboxylic groups was achieved using thioacids of different length. Surface properties were investigated by mean of water absorption analysis and static contact-angle measurements using water, diiodomethane, formamide and ethylene glycol. Blood compatibility of the PUs was evaluated by in vitro adhesion assays using 111In-radiolabeled platelet-rich plasma and [125I]fibrinogen. Morphology of the adhered platelets was examined by scanning electron microscopy (SEM). Results were compared to two biomedical-grade PUs, namely Pellethane and Tecoflex. Insertion of carboxylic groups increased surface hydrophilicity and limited water uptake ( < 8% for an ion content of 5% by weight). Surface energy of all synthesized PUs was between 40 and 45 mJ/m2. Platelet adhesion and fibrinogen adsorption on the PU anionomer surfaces were affected as a function to the increase of graft length; thiopropionic was the most haemocompatible, followed by thiosuccinic and then thioglycolic acid. SEM analyses of all ionic PU samples exhibited low platelet adhesion to surfaces with no morphological modification. In conclusion, increased hydrophily, dynamic mobility and charge repulsion are synergistic key factors for enhanced haemocompatibility. Topics: Absorption; Biocompatible Materials; Blood Platelets; Carboxylic Acids; Cell Adhesion; Cell Movement; Ethylene Glycol; Fibrinogen; Formamides; Hemolysis; Humans; Hydrocarbons, Iodinated; In Vitro Techniques; Kinetics; Magnetic Resonance Spectroscopy; Materials Testing; Microscopy, Electron, Scanning; Models, Chemical; Platelet Activation; Platelet Adhesiveness; Polyurethanes; Stereoisomerism; Surface Properties; Temperature; Time Factors; Water | 2005 |
Selection of a polyurethane membrane for the manufacture of ventricles for a totally implantable artificial heart: blood compatibility and biocompatibility studies.
Membranes made from 4 commercial poly(carbonate urethanes): Carbothane (CB), Chronoflex (CF), Corethane 80A (CT80), and Corethane 55D (CT55), and from 2 poly(ether urethanes): Tecoflex (TF) and Tecothane (TT) were prepared by solution casting and sterilized by either ethylene oxide (EO) or gamma radiation. Their biocompatibility was evaluated in vitro in terms of proliferation, cell viability, and adhesion characteristics of human umbilical veins (HUVEC), monocytes (THP-1), and skin fibroblasts, and by measuring complement activation through the generation of the C3a complex. Their hemocompatibility was determined by measuring the level of radiolabeled platelet, neutrophil, and fibrin adhesion in an ex vivo arteriovenous circuit study in piglets as well as via an in vitro hemolysis test. The results of this study showed no endothelial cell proliferation on any of the materials. The cell viability study revealed that the CB, CF, and TF membranes sterilized by EO maintained the highest percentage of monocyte viability after 72 h of incubation (>70%) while none of the gamma-sterilized membranes displayed any cell viability. The fibroblast adhesion and C3a generation assays revealed that none of the materials supported any cell adhesion or activated complement, regardless of the sterilization method. The hemolysis test also confirmed that the 4 poly(carbonate urethanes) were hemolytic while none of the poly(ether urethanes) were. Finally, the ex vivo study revealed that significantly more platelets adhered to the CB and CT55 membranes while the levels of neutrophil and fibrin deposition were observed to be similar for all 6 materials. In conclusion, the study identified the CF and TF membranes as having superior biocompatibility and hemocompatibility compared to the other polyurethanes. Topics: Animals; Biocompatible Materials; Blood; Cell Adhesion; Cell Division; Cell Survival; Complement Activation; Complement C3a; Fibrin; Fibroblasts; Heart Ventricles; Heart, Artificial; Hemolysis; Humans; Membranes, Artificial; Monocytes; Neutrophils; Platelet Adhesiveness; Polycarboxylate Cement; Polyurethanes; Prosthesis Design; Skin; Sterilization; Swine; Umbilical Veins | 2000 |