scholarly journals Bioengineering of Improved Biomaterials Coatings for Extracorporeal Circulation Requires Extended Observation of Blood-Biomaterial Interaction under Flow

2007 ◽  
Vol 2007 ◽  
pp. 1-10 ◽  
Author(s):  
Kris N. J. Stevens ◽  
Yvette B. J. Aldenhoff ◽  
Frederik H. van der Veen ◽  
Jos G. Maessen ◽  
Leo H. Koole
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Thrombus Formation ◽  
Blood Parameters ◽  
Systematic Evaluation ◽  
Loop Model ◽  
Biomaterial Surfaces ◽  
Chandler Loop ◽  
Scanning Electron

Extended use of cardiopulmonary bypass (CPB) systems is often hampered by thrombus formation and infection. Part of these problems relates to imperfect hemocompatibility of the CPB circuitry. The engineering of biomaterial surfaces with genuine long-term hemocompatibility is essentially virgin territory in biomaterials science. For example, most experiments with the well-known Chandler loop model, for evaluation of blood-biomaterial interactions under flow, have been described for a maximum duration of 2 hours only. This study reports a systematic evaluation of two commercial CPB tubings, each with a hemocompatible coating, and one uncoated control. The experiments comprised (i) testing over 5 hours under flow, with human whole blood from 4 different donors; (ii) measurement of essential blood parameters of hemocompatibility; (iii) analysis of the luminal surfaces by scanning electron microscopy and thrombin generation time measurements. The dataset indicated differences in hemocompatibility of the tubings. Furthermore, it appeared that discrimination between biomaterial coatings can be made only after several hours of blood-biomaterial contact. Platelet counting, myeloperoxidase quantification, and scanning electron microscopy proved to be the most useful methods. These findings are believed to be relevant with respect to the bioengineering of extracorporeal devices that should function in contact with blood for extended time.

Neutrophil Derived Cathepsin G Induces Potentially Thrombogenic Changes in Human Endothelial Cells: a Scanning Electron Microscopy Study in Static and Dynamic Conditions

1994 ◽  
Vol 72 (01) ◽  
pp. 140-145 ◽  
Author(s):  
Valeri Kolpakov ◽  
Maria Cristina D'Adamo ◽  
Lorena Salvatore ◽  
Concetta Amore ◽  
Alexander Mironov ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Extracellular Matrix ◽  
Endothelial Cells ◽  
Thrombus Formation ◽  
Cathepsin G ◽  
Arterial Segment ◽  
Dynamic Conditions ◽  
Activated Neutrophils ◽  
Scanning Electron

SummaryActivated neutrophils may promote thrombus formation by releasing proteases which may activate platelets, impair the fibrinolytic balance and injure the endothelial monolayer.We have investigated the morphological correlates of damage induced by activated neutrophils on the vascular wall, in particular the vascular injury induced by released cathepsin G in both static and dynamic conditions.Human umbilical vein endothelial cells were studied both in a cell culture system and in a model of perfused umbilical veins. At scanning electron microscopy, progressive alterations of the cell monolayer resulted in cell contraction, disruption of the intercellular contacts, formation of gaps and cell detachment.Contraction was associated with shape change of the endothelial cells, that appeared star-like, while the underlying extracellular matrix, a potentially thrombogenic surface, was exposed. Comparable cellular response was observed in an “in vivo” model of perfused rat arterial segment. Interestingly, cathepsin G was active at lower concentrations in perfused vessels than in culture systems. Restoration of blood flow in the arterial segment previously damaged by cathepsin G caused adhesion and spreading of platelets on the surface of the exposed extracellular matrix. The subsequent deposition of a fibrin network among adherent platelets, could be at least partially ascribed to the inhibition by cathepsin G of the vascular fibrinolytic potential.This study supports the suggestion that the release of cathepsin G by activated neutrophils, f.i. during inflammation, may contribute to thrombus formation by inducing extensive vascular damage.

scholarly journals Preparation and Characterization of PEBAX-5513/AgBF4/BMIMBF4 Membranes for Olefin/Paraffin Separation

Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1550 ◽  
Author(s):  
So Young Kim ◽  
Younghyun Cho ◽  
Sang Wook Kang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Poor Performance ◽  
Amide Group ◽  
Stabilizing Effect ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene ◽  
Scanning Electron

In this study, we investigated a poly(ether-block-amide)-5513 (PEBAX-5513)/AgBF4/1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4) composite membrane, which is expected to have a high stabilizing effect on the Ag+ ions functioning as olefin carriers in the amide group. Poly(ethylene oxide) (PEO) only consists of ether regions, whereas the PEBAX-5513 copolymer contains both ether and amide regions. However, given the brittle nature of the amide, the penetration of BMIMBF4 remains challenging. The nanoparticles did not stabilize after their formation in the long-term test, thereby resulting in a poor performance compared to previous experiments using PEO as the polymer (selectivity 3; permeance 12.3 GPU). The properties of the functional groups in the polymers were assessed using Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis, which confirmed that the properties endowed during the production of the film using the ionic liquid can impact the performance.

scholarly journals New crosslinkers for electrospun chitosan fibre mats. I. Chemical analysis

2012 ◽  
Vol 9 (75) ◽  
pp. 2551-2562 ◽  
Author(s):  
Marjorie S. Austero ◽  
Amalie E. Donius ◽  
Ulrike G. K. Wegst ◽  
Caroline L. Schauer
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Scanning Electron Microscopy ◽  
Mechanical Stability ◽  
Dissolution Tests ◽  
Natural Polysaccharide ◽  
Biomedical Field ◽  
The Stability ◽  
Scanning Electron

Chitosan (CS), the deacetylated form of chitin, the second most abundant, natural polysaccharide, is attractive for applications in the biomedical field because of its biocompatibility and resorption rates, which are higher than chitin. Crosslinking improves chemical and mechanical stability of CS. Here, we report the successful utilization of a new set of crosslinkers for electrospun CS. Genipin, hexamethylene-1,6-diaminocarboxysulphonate (HDACS) and epichlorohydrin (ECH) have not been previously explored for crosslinking of electrospun CS. In this first part of a two-part publication, we report the morphology, determined by field emission scanning electron microscopy (FESEM), and chemical interactions, determined by Fourier transform infrared microscopy, respectively. FESEM revealed that CS could successfully be electrospun from trifluoroacetic acid with genipin, HDACS and ECH added to the solution. Diameters were 267 ± 199 nm, 644 ± 359 nm and 896 ± 435 nm for CS–genipin, CS–HDACS and CS–ECH, respectively. Short- (15 min) and long-term (72 h) dissolution tests (T 600 ) were performed in acidic, neutral and basic pHs (3, 7 and 12). Post-spinning activation by heat and base to enhance crosslinking of CS–HDACS and CS–ECH decreased the fibre diameters and improved the stability. In the second part of this publication, we report the mechanical properties of the fibres.

scholarly journals Rapid induction of morphological changes in human carcinoma cells A-431 by epidermal growth factors.

1979 ◽  
Vol 83 (1) ◽  
pp. 260-265 ◽  
Author(s):  
M Chinkers ◽  
J A McKanna ◽  
S Cohen
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Growth Factors ◽  
Morphological Changes ◽  
Carcinoma Cells ◽  
Human Carcinoma ◽  
Rapid Induction ◽  
Epidermal Growth ◽  
Scanning Electron

The morphological effects of epidermal growth factor (EGF) on human carcinoma cells A-431 have been examined by scanning electron microscopy. These flat polygonal cells normally exhibit only small membrane folds, but show extensive ruffling and extension of filopodia within 5 min of exposure to EGF at 37 degrees C. This ruffling activity is transient, subsiding within another 5--15 min, but several other changes in surface morphology follow. Within the first hour of exposure to the hormone, the cell surface becomes exceedingly smooth and the nuclei seem to protrude above the plane of the otherwise thin monolayer, giving the cells a "fried egg" appearance. Cells at the edges of colonies gradually retract from the substrate, leading to reorganization, by 12 h, of the monolayer into multilayered colonies. EGF thus induces both rapid and long-term alterations in the morphology of these epidermoid cells.

Mechanisms Controlling Dormancy in the Arid Zone Grass Aristida contorta. II. Anatomy of the Hull

1974 ◽  
Vol 22 (4) ◽  
pp. 647 ◽  
Author(s):  
JJ Mott ◽  
PW Tynan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Gas Permeability ◽  
Arid Zone ◽  
Light And Electron Microscopy ◽  
Anatomical Change ◽  
Definitive Statement ◽  
Scanning Electron

The anatomy of the hull directly over the embryo was examined by light and electron microscopy in long-term dormant and non-dormant grains of A. contorta. A lipid-containing layer was noted, covering the surface of the inner epidermis of the hull, and examination by scanning electron microscopy showed that although the layer was intact in all dormant grain examined, it was fractured in non-dormant grain. A definitive statement on the function of these cracks is not possible, but they appear to be an anatomical change leading to increased gas permeability of the hull of non-dormant grains.

scholarly journals Evaluation of high-temperature corrosion on 13CrMo4-5 steel operated in the power industry

2018 ◽  
Vol 4 (21) ◽  
pp. 335-343
Author(s):  
Monika Gwoździk
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Elevated Temperature ◽  
Oxide Layer ◽  
Cross Section ◽  
High Temperature Corrosion ◽  
X Ray ◽  
Term Operation ◽  
Scanning Electron

The paper presents results of studies of steel and the oxide layer formed during a long-term operation (t=130,000h) on 13CrMo4-5 steel at an elevated temperature (T=455°C). The oxide layer was studied on a surface and a cross-section at the inner site of the pipe (in the flowing medium – steam side). The paper contains results of studies such as: light microscopy, scanning electron microscopy, X-ray phase analysis.

Scanning Electron Microscopy Study of Endothelial Injury and Thrombus Formation in WT and VWF Deficient Mice.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 3062-3062
Author(s):  
Justin Barr ◽  
Jennifer Barr ◽  
Marielle Meurice ◽  
David Motto
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Thrombus Formation ◽  
Endothelial Damage ◽  
Wild Type ◽  
Subsequent Formation ◽  
Time Points ◽  
Endothelial Surface ◽  
Deficient Mice ◽  
Scanning Electron

Abstract Abstract 3062 Poster Board II-1038 VWF is a large plasma glycoprotein required for normal hemostasis, and performs its function through binding to coagulation Factor VIII, and via interactions with both platelet surface glycoproteins and the activated and/or damaged vascular surface. We have developed a scanning electron microscopy (SEM) protocol to visualize endothelial damage and thrombus formation in wild-type and VWF-deficient mice. Thrombus formation is initiated by ferric chloride, and subsequently at defined time points, the circulation is rapidly flushed and aldehyde fixed. The carotid artery is removed, externally fixed, sectioned (both longitudinally and in cross-section), processed for SEM, and visualized. With this protocol we have obtained high-quality images (exceeding 100,000x) of FeCl3-induced endothelial damage and thrombus formation in C57BL/6 and VWF-deficient mice at baseline, and at 30, 60, 90, 120, 240, and 300 seconds post-injury (please access http://sites.google.com/site/mottolab/ to view images). Interestingly, we find that FeCl3 induces little, if any, endothelial denudation and collagen exposure at these time points, with the endothelium clearly appearing changed from baseline, but not damaged. Thus, initial platelet adhesion seems to be occurring in the absence of collagen exposure in this model. In wild-type mice, platelets adhere rapidly to the endothelial surface and assume a cross-linked appearance by 90 seconds, with continual inward growth of the thrombus through the 300 second time point. In VWF-deficient mice, platelets also adhere rapidly to the endothelial surface, but in contrast, remain recognizable longer without assuming a highly-activated phenotype. Compared with wild-type, at all time points examined the VWF-deficient thrombus appears smaller with considerably less cross-linking and platelet activation. Interestingly, during the course of these experiments we also have identified what appears to be red blood cells (RBCs) participating in thrombus formation. Similar to platelets, RBCs interact directly with the endothelial surface, and subsequently become elongated in the direction of blood flow. These elongated RBCs are often observed to cluster and bind platelets, with the subsequent formation of large platelet-erythrocyte complexes. Further characterization of these complexes and the role they may play in thrombus formation is currently in progress. Additionally, similar SEM studies are underway with both ADAMTS13-deficient and GPIb alpha-deficient mice, and with mice transiently expressing in vivo biotinylated VWF for visualization of this molecule at high magnification and resolution. These studies should help better define the mechanisms of endothelial activation and thrombus formation as they occur in situ. Disclosures No relevant conflicts of interest to declare.

Long-Term SOFCs Button Cell Testing

2013 ◽  
Vol 11 (2) ◽  
Author(s):  
Gianfranco DiGiuseppe ◽  
Li Sun
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Current Density ◽  
Electrochemical Impedance ◽  
X Ray ◽  
Total Polarization ◽  
Scanning Electron

This paper reports a new study where relatively long-term tests of about a 1000 h are performed on several planar anode-supported solid oxide fuel cells. The cell electrochemical behaviors are studied by using voltage-current density measurement, electrochemical impedance spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The cell total polarization obtained from electrochemical impedance spectroscopy results is shown to be consistent with the area-specific resistance calculated from the voltage-current density curve over the course of the test. In addition, a four-constant phase element model is used to analyze the cell components resistances at different intervals over the lifetime of the test. Scanning electron microscopy and energy-dispersive X-ray spectroscopy are used postmortem to determine if any damages occurred to the cells and to determine if any change in composition occurred to the lanthanum strontium cobalt ferrite cathode. This study shows that the tested cells remain stable with a relatively small increase in the cell total polarization but with no increase in ohmic resistance.

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