Multiscale Mechanics of Fibrin Clots

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 3089-3089
Author(s):  
Andre E.X. Brown ◽  
Rustem I. Litvinov ◽  
Prashant Purohit ◽  
Dennis E. Discher ◽  
John Weisel

Abstract Although we know a great deal about the structure, properties and many functions of fibrin(ogen), we still know very little about the microscopic and molecular origins of the clot’s mechanical properties, even though they are necessary for its functions, since hemostasis is essentially a mechanical process. In addition, it has been shown that individuals who have myocardial infarction at an early age tend to form very stiff clots. We have carried out studies at different levels of structure and integrated the results through a model that demonstrates that fibrin clot mechanical properties are manifestations of the observed mechanical characteristics of fibrin(ogen) molecules. By stretching whole fibrin clots with an extensional rheometer, we observed fibrin’s remarkable extensibility with a mechanical response that was initially linear with an increase in stiffness at larger elongation, above two-fold. These results are consistent with the large extensibility that has been observed in single fibrin fibers and may also play a role in the mechanics of blood clots at high strain, as in arterial blood flow. Furthermore, we found that protein structural transitions are required even at lower elongations. Some of the corresponding structural changes in the clots with stretching up to about four-fold were observed by electron microscopy. Scanning electron microscopy of the clots revealed extensive reorientation of the fibers making up the clots in the direction of applied stress. The orientational order was quantified from the scanning electron microscope images using a custom, automated image analysis algorithm that calculates a network order parameter, revealing a high degree of alignment for stretched, initially unoriented fibrin gels. Crosssections of stretched clots were examined by transmission electron microscopy. The most striking change observed was a huge (up to 10-fold) decrease in volume with stretching, with aggregation or bundling of fibers. Basic features of the mechanics of single fibrin fibers are known. These measurements have recently been extended to the level of single molecules using atomic force microscopy. When factor XIIIa-ligated fibrinogen oligomers were stretched by atomic force microscopy, the coiled-coils were found to unfold first under force. Until now, these observations at the molecular and fiber levels have not been correlated with the behavior of whole fibrin clots. These levels of structure were bridged through small angle X-ray fiber diffraction patterns obtained from fibrin clots, since the primary peaks in the X-ray diffraction pattern correspond to the characteristic 22.5 nm repeat distance in fibrin fibers arising from the molecular packing. In contrast to some earlier reported results, there was no change in periodicity with stretching. Instead, these peaks broadened as the sample was stretched, consistent with structural disruptions like protein unfolding while the position of the 22.5 nm peak corresponding to the fibrin repeat remained constant. Since all of these measurements are quantitative, we developed a constitutive model, including all of the features observed, that suggests that the whole clot and fiber mechanical properties are a consequence of coiled-coil unfolding. All together, this study has allowed us to develop a truly multiscale understanding of fibrin mechanics that reveals how clots or thrombi, even though they are made up of relatively stiff fibers, can still have large extensibility that allows them to withstand large strains and open and permeable structures such that they are readily lysed. Understanding how the network, fiber, and molecular properties give rise to fibrin mechanics could contribute to designs of tougher or more extensible clots or lead to new strategies for breaking up clots or making them less occlusive.

Coatings ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 652
Author(s):  
Divine Sebastian ◽  
Chun-Wei Yao ◽  
Lutfun Nipa ◽  
Ian Lian ◽  
Gary Twu

In this work, a mechanically durable anticorrosion superhydrophobic coating is developed using a nanocomposite coating solution composed of silica nanoparticles and epoxy resin. The nanocomposite coating developed was tested for its superhydrophobic behavior using goniometry; surface morphology using scanning electron microscopy and atomic force microscopy; elemental composition using energy dispersive X-ray spectroscopy; corrosion resistance using atomic force microscopy; and potentiodynamic polarization measurements. The nanocomposite coating possesses hierarchical micro/nanostructures, according to the scanning electron microscopy images, and the presence of such structures was further confirmed by the atomic force microscopy images. The developed nanocomposite coating was found to be highly superhydrophobic as well as corrosion resistant, according to the results from static contact angle measurement and potentiodynamic polarization measurement, respectively. The abrasion resistance and mechanical durability of the nanocomposite coating were studied by abrasion tests, and the mechanical properties such as reduced modulus and Berkovich hardness were evaluated with the aid of nanoindentation tests.


Materials ◽  
2020 ◽  
Vol 13 (2) ◽  
pp. 272 ◽  
Author(s):  
Verónica Gallegos-Orozco ◽  
Audel Santos-Beltrán ◽  
Miriam Santos-Beltrán ◽  
Ivanovich Estrada-Guel ◽  
Iza Ronquillo-Ornelas ◽  
...  

In the present work, nanocomposites-based 3XXX series Al alloy with three different types of hard nanoparticles, including TiO2, C, and CeO2, were produced employing two techniques such as mechanical milling and stir-casting method in order to evaluate the viability of integration of the reinforcement in the Al matrix. The integration and dispersion capability of the reinforcement into the Al alloy (3xxx Series) matrix was evaluated, using a phase angle difference and surface roughness analyses by atomic force microscopy operated in both the contact mode (CM-AFM) and tapping mode (TM-AFM), respectively. The distribution profile of both rugosity and the phase angle shift was used to statically quantify the integration and dispersion of the reinforcement into the extruded samples, by using the root mean square (RMS) parameter and phase shift coupled with the events number (EN) parameter. Results from Atomic Force Microscopy (AFM) analyses were corroborated by X-ray diffractometry and scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Microhardness tests were conducted to identify the mechanical properties of the composites in the extruded condition and their correlation with the microstructure. A close relationship was found between the microstructure obtained from the AFM and X-ray diffractometry (XRD) analyses and mechanical properties. Among all, the C reinforcement produced the major changes in the microstructure as well as the best integration and dispersion into the Al-alloy coupled with the best mechanical properties.


2008 ◽  
Vol 8 (8) ◽  
pp. 4127-4131 ◽  
Author(s):  
G. S. Okram ◽  
Kh. Namrata Devi ◽  
H. Sanatombi ◽  
Ajay Soni ◽  
V. Ganesan ◽  
...  

Nanocrystalline nickel powders were prepared with grain size 'd' in the range 40–100 nm diameters through polyol method. X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used for characterization. XRD of the prepared samples consistently matched with standard fcc structure of nickel without any impurity peak. Detailed analysis and calculations using Scherrer equation for (111) peak revealed systematic increase in line width and peak shifting towards lower diffraction 2θ angles with decrease in nickel to ethylene glycol mole ratio. Different values of d estimated from various peaks of each sample suggested associated microstrains in the nanograins. Values of d estimated from X-ray diffraction patterns were compared with those obtained from atomic force microscopy and scanning electron microscopy results, and discussed. Observed lattice expansion is explained, on the basis of a theoretical model of linear elasticity.


2008 ◽  
Vol 8 (4) ◽  
pp. 1757-1761 ◽  
Author(s):  
Ajeet Kaushik ◽  
Jitendra Kumar ◽  
M. K. Tiwari ◽  
R. Khan ◽  
B. D. Malhotra ◽  
...  

Polyaniline (PANI)–ZnO nanocomposite thin film has been successfully fabricated on glass substrates by using vacuum deposition technique. The as-grown PANI–ZnO nanocomposite thin films have been characterized using X-ray diffraction, Scanning Electron Microscopy, Atomic Force Microscopy, UV-visible spectrophotometer and Fourier Transform Infrared (FTIR) spectroscopy, respectively. X-ray diffraction of as-grown film shows the reflection of ZnO nanoparticles along with a broad peak of PANI. The surface morphology of nanocomposite films has been investigated using scanning electron microscopy and atomic force microscopy. The hypsochromic shift of the UV absorption band corresponding to π–π* transition in polymeric chain of PANI and a band at 504 cm –1 due to ZnO nanoparticles has been observed in the FTIR spectra. The hydrogen bonding between the imine group of PANI and ZnO nanoparticle has been confirmed from the presence of the absorbance band at 1151 cm–1 in the FTIR spectra of the nanocomposite thin films.


Bone ◽  
2006 ◽  
Vol 39 (3) ◽  
pp. 530-541 ◽  
Author(s):  
Mathias Hauge Bünger ◽  
Morten Foss ◽  
Kurt Erlacher ◽  
Mads Bruun Hovgaard ◽  
Jacques Chevallier ◽  
...  

2019 ◽  
Vol 946 ◽  
pp. 235-241 ◽  
Author(s):  
D.I. Tishkevich ◽  
A.I. Vorobjova ◽  
D.A. Vinnik

Through-pores alumina membranes of 50 μm thickness and 70 × 70 mm size have been fabricated to deposit Ni nanowires by electrochemical processing. Due to highly ordered microstructure of the membranes, the pores were filled by nanowires almost to 100%. The membrane nanowires composite morphology; structure and chemical features have been studied by scanning electron microscopy, atomic-force microscopy and X-ray structural analysis. To measure the specific magnetization σ as a function of temperature in the range of 77–1400 K, the pondero-motive method was used.


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