Browsing by Subject "Viscoelasticity"

Now showing 1 - 8 of 8
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    Compression-induced structural and mechanical changes of fibrin-collagen composites
    (Elsevier, 2017-07) Kim, O. V.; Litvinov, R. I.; Chen, J.; Chen, D. Z.; Weisel, J.W.; Alber, M. S.; Medicine, School of Medicine
    Fibrin and collagen as well as their combinations play an important biological role in tissue regeneration and are widely employed in surgery as fleeces or sealants and in bioengineering as tissue scaffolds. Earlier studies demonstrated that fibrin-collagen composite networks displayed improved tensile mechanical properties compared to the isolated protein matrices. Unlike previous studies, here unconfined compression was applied to a fibrin-collagen filamentous polymer composite matrix to study its structural and mechanical responses to compressive deformation. Combining collagen with fibrin resulted in formation of a composite hydrogel exhibiting synergistic mechanical properties compared to the isolated fibrin and collagen matrices. Specifically, the composite matrix revealed a one order of magnitude increase in the shear storage modulus at compressive strains>0.8 in response to compression compared to the mechanical features of individual components. These material enhancements were attributed to the observed structural alterations, such as network density changes, an increase in connectivity along with criss-crossing, and bundling of fibers. In addition, the compressed composite collagen/fibrin networks revealed a non-linear transformation of their viscoelastic properties with softening and stiffening regimes. These transitions were shown to depend on protein concentrations. Namely, a decrease in protein content drastically affected the mechanical response of the networks to compression by shifting the onset of stiffening to higher degrees of compression. Since both natural and artificially composed extracellular matrices experience compression in various (patho)physiological conditions, our results provide new insights into the structural biomechanics of the polymeric composite matrix that can help to create fibrin-collagen sealants, sponges, and tissue scaffolds with tunable and predictable mechanical properties.
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    Dual Functionalization of Gelatin for Orthogonal and Dynamic Hydrogel Cross-Linking
    (American Chemical Society, 2021) Kim, Min Hee; Nguyen, Han; Chang, Chun-Yi; Lin, Chien-Chi; Biomedical Engineering, School of Engineering and Technology
    Gelatin based hydrogels are widely used in biomedical fields owing to its abundance of bioactive motifs that support cell adhesion and matrix remodeling. While inherently bioactive, unmodified gelatin exhibits temperature-dependent rheology and solubilizes at body temperature, making it unstable for three-dimensional (3D) cell culture. Therefore, the addition of chemically reactive motifs is required to render gelatin-based hydrogels with highly controllable crosslinking kinetics and tunable mechanical properties that are critical for 3D cell culture. This article provides a series of methods toward establishing orthogonally crosslinked gelatin-based hydrogels for dynamic 3D cell culture. In particular, we prepared dually functionalized gelatin macromers amenable for sequential, orthogonal covalent crosslinking. Central to this material platform is the synthesis of norbornene-functionalized gelatin (GelNB), which forms covalently crosslinked hydrogels via orthogonal thiol-norbornene click crosslinking. Using GelNB as the starting material, we further detail the methods for synthesizing gelatin macromers susceptible to hydroxyphenylacetic acid (HPA) dimerization (i.e., GelNB-HPA) and hydrazone bonding (i.e., GelNB-CH) for on-demand matrix stiffening. Finally, we outline the protocol for synthesizing a gelatin macromer capable of adjusting hydrogel stress-relaxation via boronate ester bonding (i.e., GelNB-BA). The combinations of these orthogonal chemistries affords a wide range of gelatin based hydrogels as biomimetic matrices in tissue engineering and regenerative medicine applications.
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    Effects of stress-dependent growth on evolution of sulcal direction and curvature in models of cortical folding
    (Elsevier, 2023) Balouchzadeh, Ramin; Bayly, Philip V.; Garcia, Kara E.; Radiology and Imaging Sciences, School of Medicine
    The majority of human brain folding occurs during the third trimester of gestation. Although many studies have investigated the physical mechanisms of brain folding, a comprehensive understanding of this complex process has not yet been achieved. In mechanical terms, the "differential growth hypothesis" suggests that the formation of folds results from a difference in expansion rates between cortical and subcortical layers, which eventually leads to mechanical instability akin to buckling. It has also been observed that axons, a substantial component of subcortical tissue, can elongate or shrink under tensile or compressive stress, respectively. Previous work has proposed that this cell-scale behavior in aggregate can produce stress-dependent growth in the subcortical layers. The current study investigates the potential role of stress-dependent growth on cortical surface morphology, in particular the variations in folding direction and curvature over the course of development. Evolution of sulcal direction and mid-cortical surface curvature were calculated from finite element simulations of three-dimensional folding in four different initial geometries: (i) sphere; (ii) axisymmetric oblate spheroid; (iii) axisymmetric prolate spheroid; and (iv) triaxial spheroid. The results were compared to mid-cortical surface reconstructions from four preterm human infants, imaged and analyzed at four time points during the period of brain folding. Results indicate that models incorporating subcortical stress-dependent growth predict folding patterns that more closely resemble those in the developing human brain. Statement of significance: Cortical folding is a critical process in human brain development. Aberrant folding is associated with disorders such as autism and schizophrenia, yet our understanding of the physical mechanism of folding remains limited. Ultimately mechanical forces must shape the brain. An important question is whether mechanical forces simply deform tissue elastically, or whether stresses in the tissue modulate growth. Evidence from this paper, consisting of quantitative comparisons between patterns of folding in the developing human brain and corresponding patterns in simulations, supports a key role for stress-dependent growth in cortical folding.
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    A rate insensitive linear viscoelastic model for soft tissues
    (Elsevier, 2007-08) Zhang, Wei; Chen, Henry Y.; Kassab, Ghassan S.; Department of Biomedical Engineering, School of Engineering and Technology
    It is well known that many biological soft tissues behave as viscoelastic materials with hysteresis curves being nearly independent of strain rate when loading frequency is varied over a large range. In this work, the rate insensitive feature of biological materials is taken into account by a generalized Maxwell model. To minimize the number of model parameters, it is assumed that the characteristic frequencies of Maxwell elements form a geometric series. As a result, the model is characterized by five material constants: μ0, τ, m, ρ and β, where μ0 is the relaxed elastic modulus, τ the characteristic relaxation time, m the number of Maxwell elements, ρ the gap between characteristic frequencies, and β = μ1/μ0 with μ1 being the elastic modulus of the Maxwell body that has relaxation time τ. The physical basis of the model is motivated by the microstructural architecture of typical soft tissues. The novel model shows excellent fit of relaxation data on the canine aorta and captures the salient features of vascular viscoelasticity with significantly fewer model parameters.
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    A rate-insensitive linear viscoelastic model for soft tissues
    (Elsevier, 2007-08) Zhang, Wei; Chen, Henry Y.; Kassab, Ghassan S.; Department of Biomedical Engineering, School of Engineering and Technology
    It is well known that many biological soft tissues behave as viscoelastic materials with hysteresis curves being nearly independent of strain rate when loading frequency is varied over a large range. In this work, the rate-insensitive feature of biological materials is taken into account by a generalized Maxwell model. To minimize the number of model parameters, it is assumed that the characteristic frequencies of Maxwell elements form a geometric series. As a result, the model is characterized by five material constants: micro(0), tau, m, rho and beta, where micro(0) is the relaxed elastic modulus, tau the characteristic relaxation time, m the number of Maxwell elements, rho the gap between characteristic frequencies, and beta=micro(1)/micro(0) with micro(1) being the elastic modulus of the Maxwell body that has relaxation time tau. The physical basis of the model is motivated by the microstructural architecture of typical soft tissues. The novel model shows excellent fit of relaxation data on the canine aorta and captures the salient features of vascular viscoelasticity with significantly fewer model parameters.
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    Resonant acoustic rheometry for assessing plasma coagulation in bleeding patients
    (Springer Nature, 2025-02-11) Li, Weiping; Bunch, Connor M.; Zackariya, Sufyan; Patel, Shivani S.; Buckner, Hallie; Condon, Shaun; Walsh, Matthew R.; Miller, Joseph B.; Walsh, Mark M.; Hall, Timothy L.; Jin, Jionghua; Stegemann, Jan P.; Deng, Cheri X.; Emergency Medicine, School of Medicine
    Disordered hemostasis associated with life-threatening hemorrhage commonly afflicts patients in the emergency department, critical care unit, and perioperative settings. Rapid and sensitive hemostasis phenotyping is needed to guide administration of blood components and hemostatic adjuncts to reverse aberrant hemostasis. Here, we report the use of resonant acoustic rheometry (RAR), a technique that quantifies the viscoelastic properties of soft biomaterials, for assessing plasma coagulation in a cohort of 38 bleeding patients admitted to the hospital. RAR captured the dynamic characteristics of plasma coagulation that were dependent on coagulation activators or reagent conditions. RAR coagulation parameters correlated with TEG reaction time and TEG functional fibrinogen, especially when stratified by comorbidities. A quadratic classifier trained on selective RAR parameters predicted transfusion of fresh frozen plasma and cryoprecipitate with modest to high overall accuracy. While these results demonstrate the feasibility of RAR for plasma coagulation and utility of a machine learning model, the relative small number of patients, especially the small number of patients who received transfusion, is a limitation of this study. Further studies are need to test a larger number of patients to further validate the capability of RAR as a cost-effective and sensitive hemostasis assay to obtain quantitative data to guide clinical-decision making in managing severely hemorrhaging patients.
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    The significance of loading profile on the occlusion mechanics of a viscoelastic periodontal ligament analogue-supported tooth
    (2020-06) Thompson, James P.; Katona, Thomas R.; Eckert, George J.
    Background: Benchtop studies of occlusal contact forces have used teeth that were rigidly attached or supported by readily available viscoelastic (VE) materials that served as periodontal ligament (PDL) substitutes. More recent specimens have incorporated a precisely dimensioned VE PDL-behavior matched analogue. Objectives: The objectives of this study were to evaluate a modified loading protocol (step function) that is more appropriate to VE support than the previously used ramp function. The occlusion manifestations of the time-dependent behaviors (creep and recovery) of the PDL analogue were examined using the revised protocol. Methods: A mandibular 1st molar denture tooth was set into a precision-machined root/socket assembly. The PDL substitute was then cured to tight dimensional tolerances. The matching rigidly fixed maxillary denture tooth was aligned into a Class I centric molar relationship in a testing apparatus. The weighted maxillary assembly was then cycled onto and off of the load cell-supported mandibular assembly. For statistical purposes, three loading schedules were tested in 21 0.05 mm shifted occlusal relationships. Rigid attachment served as control. Results: Statistical analyses were performed on the peak values of Flateral, the net in-occlusal plane force component of the occlusal contact forces. It was found that there were statistically significant differences between: chomp-to-chomp (p < .038), PDL vs. rigid (p < .001) and loading schedules (p < .044 for PDL only). Conclusion: The loading protocol affects outcomes, and the step functions maintained consistent timing with prescribable creep and recovery periods.
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    Viscoelastic hydrogels for interrogating pancreatic cancer-stromal cell interactions
    (Elsevier, 2023-02-04) Lin, Fang-Yi; Chang, Chun-Yi; Nguyen, Han; Li, Hudie; Fishel, Melissa L.; Lin, Chien-Chi; Pediatrics, School of Medicine
    The tumor microenvironment (TME) is known to direct cancer cell growth, migration, invasion into the matrix and distant tissues, and to confer drug resistance in cancer cells. While multiple aspects of TME have been studied using in vitro, ex vivo, and in vivo tumor models and engineering tools, the influence of matrix viscoelasticity on pancreatic cancer cells and its associated TME remained largely unexplored. In this contribution, we synthesized a new biomimetic hydrogel with tunable matrix stiffness and stress-relaxation for evaluating the effect of matrix viscoelasticity on pancreatic cancer cell (PCC) behaviors in vitro. Using three simple monomers and Reverse-Addition Fragmentation Chain-Transfer (RAFT) polymerization, we synthesized a new class of phenylboronic acid containing polymers (e.g., poly (OEGA-s-HEAA-s-APBA) or PEHA). Norbornene group was conjugated to HEAA on PEHA via carbic anhydride, affording a new NB and BA dually modified polymer - PEHNBA amenable for orthogonal thiol-norbornene photopolymerization and boronate ester diol complexation. The former provided tunable matrix elasticity, while the latter gave rise to matrix stress-relaxation (or viscoelasticity). The new PEHNBA polymers were shown to be highly cytocompatible for in situ encapsulation of PCCs and cancer-associated fibroblasts (CAFs). Furthermore, we demonstrated that hydrogels with high stress-relaxation promoted spreading of CAFs, which in turns promoted PCC proliferation and spreading in the viscoelastic matrix. Compared with elastic matrix, viscoelastic gels upregulated the secretion of soluble proteins known to promote epithelial-mesenchymal transition (EMT). This study demonstrated the crucial influence of matrix viscoelasticity on pancreatic cancer cell fate and provided an engineered viscoelastic matrix for future studies and applications related to TME.