Methyl cellulose (MC) is a widely used material in various microfluidic applications in biology. Due to its biocompatibility, it has become a popular crowding agent for microfluidic cell deformability measurements, which usually operate at high shear rates (> 10,000 s^-1). However, a full rheological characterization of methyl cellulose solutions under these conditions has not yet been reported. With this study, we provide a full shear-rheological description for solutions of up to 1% MC dissolved in phosphate-buffered saline (PBS) that are commonly used in real-time deformability cytometry (RT-DC). We characterized three different MC-PBS solutions used for cell mechanical measurements in RT-DC with three different shear rheometer setups to cover a range of shear rates from 0.1-150,000 s^-1. We report viscosities and normal stress differences in this regime. Viscosity functions can be well described using a Carreau-Yasuda model. Furthermore, we present the temperature dependency of shear viscosity and first normal stress difference of these solutions. Our results show that methyl cellulose solutions behave like power-law liquids in viscosity and first normal stress difference at shear rates between 5,000-150,000 s^-1. We construct a general viscosity equation for each MC solution at a certain shear rate and temperature. Furthermore, we investigated how MC concentration influences the rheology of the solutions and found the entanglement concentration at around 0.64 w/w%. Our results help to better understand the viscoelastic behavior of MC solutions, which can now be considered when modelling stresses in microfluidic channels.

We study the incipient motion of single spheres in steady shear flow on regular substrates at low particle Reynolds numbers. The substrate consists of a monolayer of regularly arranged fixed beads, in which the spacing between beads is varied resulting in different angles of repose and exposures of the particle to the main flow. The flow-induced forces and the level of flow penetration into the substrate are determined numerically. Since experiments in this range had shown that the critical Shields number is independent of inertia but strongly dependent on the substrate geometry, the particle Reynolds number was fixed to 0.01 in the numerical study. Numerics indicates that rolling motion is always preferred to sliding and that the flow penetration is linearly dependent on the spacing between the substrate particles. Besides, we propose an analytical model for the incipient motion. The model is an extension of Goldman’s classical result for a single sphere near a plain surface taking into account the angle of repose, flow orientation with respect to substrate topography and shielding of the sphere to the linear shear flow. The effective level of flow penetration is the only external parameter. The model, applied to triangular and quadratic arrangements with different spacings, is able to predict the dependence of the critical Shields number on the geometry and on the orientation of the substrate. The model is in very good agreement with numerical results. For well-exposed particles, we observed that the minimum critical Shields number for a certain angle of repose does not depend sensitively on the considered arrangement. At large angles of repose, as expected in fully armoured beds, the model is consistent with experimental results for erodible beds at saturated conditions.

We study aqueous xanthan solutions at shear rates up to about 105 s−1. At these shear rates, the salt-free solutions show an infinite-shear viscosity plateau. Depending on the xanthan concentration, we find two different regimes with scaling laws well known for the zero-shear viscosity of dilute and semidilute solutions: The crossover concentration is considerably higher than in the first Newtonian branch, which can be related to the orientation of the polyelectrolytes. In the second regime, the normal stress differences increase with an exponent of about 1, indicating that the polymer solution behaves like nematic liquid crystals or rigid fiber suspensions. In the first regime, the exponent is smaller suggesting that the polyelectrolytes behave more flexible.

We study buffered aqueous solutions of deoxyribonucleic acid isolated from bacteriophage lambda (λ-DNA) at shear rates up to 105 s−1. The shear rates are accessed with a narrow-gap rheometer at gap widths down to 20 μm. At lower shear rates, our data merge with the literature values. At high shear rates, the viscosity levels off into an infinite-shear viscosity plateau. Hence, the viscosity functions of buffered aqueous DNA solutions are now available for the entire shear-rate range from the first Newtonian plateau to that of infinite-shear viscosity. The latter hardly differs from the solvent viscosity. For the normal-stress differences, we observe a power-law dependence on the shear rate close to previous findings up to shear rates of about 104 s−1. Beyond this shear-rate range, we observe a stepwise change with the shear rate. By means of agarose gel electrophoresis, we confirm that the λ-DNA is not fragmented during our rheometric study at high shear rates. Yet, at the highest shear rates studied, shear-induced changes in the DNA to structures not being able to travel through the gel appear.

Biological molecules in nutraceuticals and functional foods have proven physiological properties to treat human chronic diseases. These molecules contribute to applications in the food and pharmaceutical industries by preventing food spoilage and cellular injury. Technological advancement in the screening and characterization of bioactive peptides has enabled scientists to understand the associated molecules. Consistent collaboration among nutritionists, pharmacists, food scientists, and bioengineers to find new bioactive compounds with higher therapeutic potential against nutrition-related diseases highlights the potential of the bioactive peptides for food and pharmaceutic industries. Among the popular dietary supplements, marine animals have always been considered imperative due to their rich nutritional values and byproduct use in the food and pharmaceutical industries. The bioactive peptides isolated from marine animals are well-known for their higher bioactivities against human diseases. The physiological properties of fish-based hydrolyzed proteins and peptides have been claimed through in vitro, in vivo, and clinical trials. However, systematic study on the physiological and clinical significance of these bioactive peptides is scarce. In this review, we not only discuss the physiological and clinical significance of antioxidant and anticancer peptides derived from marine animals, but we also compare their biological activities through existing in vitro and in vivo studies.