silicon and Hemolysis

The primary goal of our investigation was the development of a versatile immobilization matrix based on archaeal tetraether lipids that meets the most important prerequisites to render an implant surface bioactive by binding specific functional groups or functional polymers with the necessary flexibility and an optimal spatial arrangement to be bioavailable. From this point of view, it appears obvious that numerous efforts made recently to avoid initial bacterial adhesion on catheter surfaces as an important prerequisite of material associated infection episodes have shown only a limited efficiency since the bioactive entities could not be presented in an optimal conformation and a stable density. A significant improvement of this situation can be achieved by highly specific biomimetic modifications of the catheter surfaces. The term "biomimetic" originates from the fact that specific archaeal tetraether lipids were introduced to form a membrane analog monomolecular spacer system, which (1) can be immobilized on nearly all solid surfaces and (2) chemically modified to present a tailor-made functionality in contact with aqueous media either to avoid or inhibit surface fouling or to equip any implant surface with the necessary chemical functionality to enable cell adhesion and tissue integration. Ultrathin films based on tetraether lipids isolated from archaea Thermoplasma acidophilum were used as a special biomimetic immobilization matrix on the surface of commercial medical silicon elastomers. A complete performance control of the membrane analog coatings was realized in addition to biofunctionality tests, including the proof of cytotoxicity and hemocompatibility according to DIN EN ISO 10993. In order to make sure that the developed immobilization matrix including the grafted functional groups are biocompatible under in vivo-conditions, specific animal tests were carried out to examine the in vivo-performance. It can be concluded that the tetraether lipid based coating systems on silicone have shown no signs of cytotoxicity and a good hemocompatibility. Moreover, no mutagenic effects, no irritation effects, and no sensitization effects could be demonstrated. After an implantation period of 28 days, no irregularities were found.

Topics: Animals; Biomimetic Materials; Cell Line; Cell Survival; Coated Materials, Biocompatible; Hemolysis; Humans; Lipid Metabolism; Lipids; Membranes; Mice; Prostheses and Implants; Rabbits; Silicon; Surface Properties; Thermoplasma

Due to their outstanding properties, quantum dots (QDs) received a growing interest in the biomedical field, but it is of major importance to investigate and to understand their interaction with the biomolecules. We examined the stability of silicon QDs and the time evolution of QDs - protein corona formation in various biological media (bovine serum albumin, cell culture medium without or supplemented with 10% fetal bovine serum-FBS). Changes in the secondary structure of BSA were also investigated over time. Hydrodynamic size and zeta potential measurements showed an evolution in time indicating the nanoparticle-protein interaction. The protein corona formation was also dependent on time, albumin adsorption reaching the peak level after 1 hour. The silicon QDs adsorbed an important amount of FBS proteins from the first 5 minutes of incubation that was maintained for the next 8 hours, and diminished afterwards. Under protein-free conditions the QDs induced cell membrane damage in a time-dependent manner, however the presence of serum proteins attenuated their hemolytic activity and maintained the integrity of phosphatidylcholine layer. This study provides useful insights regarding the dynamics of BSA adsorption and interaction of silicon QDs with proteins and lipids, in order to understand the role of QDs biocorona.

Topics: Adsorption; Animals; Cattle; Hemolysis; Humans; Protein Corona; Protein Structure, Secondary; Quantum Dots; Serum Albumin, Bovine; Silicon; Silicon Dioxide

Silk-based medical products have a long history of use as a material for surgical sutures because of their desirable mechanical properties. However, silk fibroin fabric has been reported to be haemolytic when in direct contact with blood. The layer-by-layer self-assembly technique provides a method for surface modification to improve the biocompatibility of silk fibroin fabrics. Regenerated silk fibroin and alginate, which have excellent biocompatibility and low immunogenicity, are outstanding candidates for polyelectrolyte deposition. In this study, silk fabric was degummed and positively charged to create a silk fibroin fabric that could undergo self-assembly. The multilayer self-assembly of the silk fibroin fabric was achieved by alternating the polyelectrolyte deposition of a negatively charged alginate solution (pH = 8) and a positively charged regenerated silk fibroin solution (pH = 2). Finally, the negatively charged regenerated silk fibroin solution (pH = 8) was used to assemble the outermost layer of the fabric so that the surface would be negatively charged. A stable structural transition was induced using 75% ethanol. The thickness and morphology were characterised using atomic force microscopy. The properties of the self-assembled silk fibroin fabric, such as the bursting strength, thermal stability and flushing stability, indicated that the fabric was stable. In addition, the cytocompatibility and haemocompatibility of the self-assembled silk fibroin fabrics were evaluated. The results indicated that the biocompatibility of the self-assembled multilayers was acceptable and that it improved markedly. In particular, after the self-assembly, the fabric was able to prevent platelet adhesion. Furthermore, other non-haemolytic biomaterials can be created through self-assembly of more than 1.5 bilayers, and we propose that self-assembled silk fibroin fabric may be an attractive candidate for anticoagulation applications and for promoting endothelial cell adhesion for vascular prostheses.

Topics: Alginates; Animals; Electrolytes; Fibroins; Glucuronic Acid; Hemolysis; Hexuronic Acids; Humans; Hydrogen-Ion Concentration; Materials Testing; Microscopy, Atomic Force; Platelet Adhesiveness; Silicon; Spectroscopy, Fourier Transform Infrared; Static Electricity; Surface Properties; Sus scrofa; Temperature; Textiles; Thermogravimetry

Despite steadily increasing insights on the biocompatibility of PSi nanoparticles (NPs), an extensive biosafety study on the immune and red blood cells (RBCs) is still lacking. Herein, we evaluated the impact of the PSi NPs' surface chemistry on immune cells and human RBCs both in vitro and in vivo. Negatively charged hydrophilic and hydrophobic PSi NPs caused less ATP depletion and genotoxicity than the positively charged amine modified hydrophilic PSi NPs, demonstrating the main role of PSi NPs' surface charge on the immunocompatibility profile. Furthermore, cells with lower metabolic activity, longer doubling time, and shorter half-life were more sensitive to the concentration- and time-dependent toxicity in the following order: T-cells ≈ monocytes > macrophages ≈ B-cells. RBC hemolysis and imaging assay revealed a significant correlation between the surface chemistry, the amount of the PSi NPs adsorbed on the cell surface and the extent of morphological changes. The in vivo results showed that despite mild renal steatosis, glomerular degeneration, hepatic central vein dilation and white pulp shrinkage in spleen, no notable changes were observed in the serum level of biochemical and hematological factors. This study is a comprehensive demonstration of the mechanistic direct and indirect genotoxicity effects of PSi NPs, elucidating the most influencing properties for the PSi NPs' design.

Topics: Animals; B-Lymphocytes; Cell Line; Erythrocytes; Hemolysis; Humans; Male; Mice; Microscopy, Electrochemical, Scanning; Nanoparticles; Rats; Rats, Sprague-Dawley; Silicon

Recently, it has been shown that heat-shock protein 70 (hsp70) functions in a dual role as a chaperone and a cytokine. However, no information is available on the occurrence of hsp70 in the extracellular milieu or on its ability to modulate cellular immune response. This study shows a material-dependent increase of hsp70 levels in plasma following contact of fresh heparinized whole human blood with three different biomaterials (PVC, heparin-coated PVC, Silicone). We report a previously unknown behavior of hsp70 to act as a plasma-adsorption protein. Further, high binding capacities for hsp70 to artificial surfaces (measured by Western blotting) and elevated hsp70 levels in plasma (measured by EIA) following contact with blood correspond with a reduced hemocompatibility. The degree of surface-induced activation of blood was determined by analysis of markers for coagulation, inflammation and complement activation. These findings indicate that the selective adsorption of hsp70 on artificial surfaces and the increased hsp70 levels in plasma may be important in directing host inflammatory and immune responses. We suggest that the levels of hsp70 in human plasma may represent a new prognostic factor or a diagnostic biomarker in hemostasis research.

Topics: Adsorption; beta-Thromboglobulin; Biomarkers; Blood; Blood Proteins; Complement C3; Fibrinogen; Gene Expression Regulation; Hemolysis; Hemostasis; Heparin; HSP70 Heat-Shock Proteins; Humans; Interleukins; Monocytes; Polyvinyl Chloride; Silicon; Solubility; Time Factors; Tumor Necrosis Factor-alpha

We have been developing a centrifugal blood pump with a magnetically suspended impeller. To improve pump efficiency, we investigated the pump performances of many kinds of impeller vanes and diffusers, as well as the flow in the gap between the impeller discs and the pump housing. We found the vanes and the diffusers with high pump efficiency; however, high efficiency does not mean low hemolysis. It seems important to prevent generation of small-sized eddies with high shear stress. Hemolysis tests are carried out to find the optimal vane profile and gap clearance. The index of hemolysis and temperature change of our pump is better than those of the Biopump. Short-term in vivo studies show that the layer of white thrombi adheres to the machined rough surface of polycarbonate, which composes the narrow gap (0.2 mm) between the impeller and the pump wall, but a smooth surface coated with silicon prevents adhesion of that layer.

Topics: Animals; Blood Cells; Cell Adhesion; Electromagnetic Fields; Heart-Assist Devices; Hemolysis; Platelet Aggregation; Sheep; Silicon; Temperature; Thrombosis

Silicates causing pneumoconiosis function as Fenton catalysts to generate hydroxyl radicals (.OH) when incubated with hydrogen peroxide and a reducing substance. In contrast, silicates which do not cause pneumoconiosis demonstrate no Fenton activity. Catalytic activity is decreased by pretreatment of silicates with the iron chelators deferoxamine or transferrin. Hemolysis from silicates is decreased by interventions which remove superoxide anion or hydrogen peroxide from the medium, or by pretreatment of dusts with iron chelators. Thus, asbestos and nonfibrous silicates may cause pneumoconiosis through a common oxidant mechanism by catalyzing production of toxic .OH radicals in the lung.

Topics: Catalysis; Dust; Erythrocyte Membrane; Free Radicals; Hemolysis; Humans; Hydrogen Peroxide; Hydroxides; Hydroxyl Radical; Iron; Pneumoconiosis; Silicon

The haemolytic potential of attapulgite (Senegal) has been investigated. When the particles were pretreated with dipalmitoyl phosphatidylcholine (DPPC) or with bovine serum albumin (BSA) at a concentration that would obtain maximum coverage of the particles by adsorption, a change in haemolysis was observed. The results indicate that haemolysis is strongly dependent on the surface state of the particles.

Topics: 1,2-Dipalmitoylphosphatidylcholine; Hemolysis; Humans; Kinetics; Magnesium; Magnesium Compounds; Serum Albumin, Bovine; Silicon; Silicon Compounds

The membranolytic and cytotoxic properties of two naturally occurring (chrysotile asbestos; attapulgite clay) and two man-made (Fiberfrax, an aluminium-silicate, and xonotlite, a calcium silicate) industrial minerals were compared. "Short" fiber fractions of chrysotile and Fiberfrax were obtained by sedimentation in demineralized water, while the attapulgite and xonotlite samples were used as obtained. The aluminium silicate fibers were found to be non- hemolytic, while for the other three silicates, chrysotile had the strongest hemolysis potential, followed very closely by xonotlite; attapulgite was less hemolytic than the former two silicates, but was nevertheless highly hemolytic to the rat erythrocytes. Using rat pulmonary alveolar macrophages, the in vitro cytotoxicity assays showed that with fresh cell monolayers, all four silicates were equivalent in causing cell damages at a dose of 250 micrograms; at a lower dose (50 micrograms), the intensity of the cytotoxic effect was in the decreasing order: Fiberfrax greater than attapulgite greater than chrysotile greater than xonotlite. With one day-old cultured cell monolayers, a dose of 250 micrograms of the silicates fibers was less cytotoxic, with the exception of the attapulgite fibers which remained essentially as cytotoxic as with the fresh cell monolayers. The reduced cytotoxic response was especially noticeable with the chrysotile fibers. At 50 micrograms, the cytotoxicity scale of the mineral dusts with one day-old cell monolayers was essentially the same as the one obtained with the fresh cell monolayers, that is: Fiberfrax approximately equal to attapulgite greater than chrysotile greater than or equal to xonotlite. Overall, these in vitro tests imply: 1) that all four industrial silicates tested can be considered to be "biologically active"; 2) that on the basis of their different reactivities with the two types of cell culture conditions used, their biological reactivity in vivo might be quite distinct. This might be especially true for at least the chrysotile, attapulgite and xonotlite short fibers, considering that these three types of silicate dusts have very similar dimensions. Moreover, for the chrysotile and attapulgite samples, fiber numbers is probably not an important factor, since the density of the two silicates is roughly the same. The unaltered cytotoxic responses of the American attapulgite fibers in the two macrophage assays correlate well with the fact that short attapulgite f

Topics: Animals; Asbestos; Asbestos, Serpentine; Calcium Compounds; Cell Survival; Cells, Cultured; Dust; Hemolysis; L-Lactate Dehydrogenase; Lactates; Macrophages; Magnesium; Magnesium Compounds; Particle Size; Pulmonary Alveoli; Rats; Silicates; Silicic Acid; Silicon; Silicon Compounds; Silicon Dioxide

Haemolytic activities and effects on alveolar macrophages (AM) of various fibres were studied. UICC asbestos fibres and attapulgites either untreated or acid-leached were used. Amphiboles and commercial attapulgites were both cytotoxic on AM, but attapulgites and chrysotile were only haemolytic. Chrysotile fibres induced a release of B galactosidase; when acid treated these fibres were cytotoxic and less haemolytic. Acid treated amphiboles were more haemolytic than untreated.

Topics: Asbestos; Asbestos, Amphibole; beta-Galactosidase; Erythrocytes; Hemolysis; In Vitro Techniques; Macrophages; Magnesium; Magnesium Compounds; Pulmonary Alveoli; Silicon; Silicon Compounds; Silicon Dioxide

We have evaluated a serum separator device that is designed to effect better separation and isolation of serum from clotted blood. This device consists of an evacuated blood-drawing tube (Vacutainer) containing 1.5 ml of a semi-solid silicon polymer that forms a barrier between serum and clot during centrifugation. We compared test specimens with conventionally processed (Vacutainer) specimens as controls. Eighty-one chemical, toxicological, and immunological reactions, tests, or methods were studied. For several tests we observed changes that are statistically but not clinically significant. The one clinically significant change in serum chemistry values occurred in the case of lactate dehydrogenase, for which values were increased by 5-8% of the upper limit of normal.

Topics: Blood Chemical Analysis; Blood Coagulation; Blood Protein Electrophoresis; Blood Specimen Collection; Evaluation Studies as Topic; Hemolysis; Humans; L-Lactate Dehydrogenase; Protein Conformation; Silicon

Topics: Age Factors; Animals; Calcium; Caseins; Citrates; Cytological Techniques; Edetic Acid; Glycolysis; Guinea Pigs; Hemolysis; Heparin; Lactates; Leukocytes; Magnesium; Male; Silicon; Temperature

Topics: Animals; Asbestos; Edetic Acid; Erythrocytes; Hemolysis; Hydrogen-Ion Concentration; In Vitro Techniques; Macrophages; Magnesium; Neuraminic Acids; Neuraminidase; Oxides; Polyvinyls; Pyridines; Sheep; Silicon