Device for rheometry, impedance spectroscopy, and electrochemistry on fluid electrodes

We describe the extension of a rheometer to enable in situ impedance spectroscopy and electrochemical cycling. Key advantages of this instrument over traditional flow-channel based methods for studying fluid electrodes are the possibilities to monitor the rheological properties during cycling as well as to control the mechanical history of the sample. We describe two electrochemical configurations of the instrument, allowing fluid electrodes to be studied as full and half-cells. To demonstrate the systems' capabilities, we present characterizations of 4 different fluid electrode systems

Dynamics of ballistically injected latex particles in living human endothelial cells

We studied the dynamics of ballistically injected latex particles (BIP) inside endothelial cells, using video particle tracking to measure the mean squared displacement (MSD) as a function of lag time. The MSD shows a plateau at short times and a linear behavior at longer times, indicating that the BIP are trapped into a viscoelastic network. To reveal more about the molecular constituents and the dynamics of this actin network, we added a variety of drugs. Latrunculin and Jasplakinolide aimed at intervening with the actin network caused a strong increase in MSD, whereas Taxol aimed at microtubules gave no measurable change in MSD. Additional corroborating information about these drug effects were obtained from MSD amplitude and exponent distributions and from fluorescent staining images of the actin and microtubule networks. Our evidence strongly suggests that BIP are primarily embedded in the actin network. Additional drug interventions aimed at disabling non-thermal forces could not conclusively resolve the nature of the forces driving BIP dynamics

Ultrasensitive Detection and in Situ Imaging of Analytes on Graphene Oxide Analogues Using Enhanced Raman Spectroscopy

[Image: see text] We demonstrate how algorithm-improved confocal Raman microscopy (ai-CRM), in combination with chemical enhancement by two-dimensional substrates, can be used as an ultrasensitive detection method for rhodamine (R6G) molecules adsorbed from aqueous solutions. After developing a protocol for laser-induced reduction of graphene oxide, followed by noninvasive Raman imaging, a limit of detection (LOD) of 5 × 10(–10) M R6G was achieved using ai-CRM. An equivalent subnanomolar LOD was also achieved on another graphene oxide analogue −UV/ozone-oxidized graphene. These record-breaking detection capabilities also enabled us to study the adsorption kinetics and image the spatial distribution of the adsorbed R6G. These findings indicate a strong potential for algorithm-improved graphene-enhanced Raman spectroscopy as a facile method for detecting, imaging, and quantifying trace amounts of adsorbing molecules on a variety of 2D substrates

Microfluidics as a functional tool for cell mechanics

Living cells are a fascinating demonstration of nature’s most intricate and well-coordinated micromechanical objects. They crawl, spread, contract, and relax—thus performing a multitude of complex mechanical functions. Alternatively, they also respond to physical and chemical cues that lead to remodeling of the cytoskeleton. To understand this intricate coupling between mechanical properties, mechanical function and force-induced biochemical signaling requires tools that are capable of both controlling and manipulating the cell microenvironment and measuring the resulting mechanical response. In this review, the power of microfluidics as a functional tool for research in cell mechanics is highlighted. In particular, current literature is discussed to show that microfluidics powered by soft lithographic techniques offers the following capabilities that are of significance for understanding the mechanical behavior of cells: (i) Microfluidics enables the creation of in vitro models of physiological environments in which cell mechanics can be probed. (ii) Microfluidics is an excellent means to deliver physical cues that affect cell mechanics, such as cell shape, fluid flow, substrate topography, and stiffness. (iii) Microfluidics can also expose cells to chemical cues, such as growth factors and drugs, which alter their mechanical behavior. Moreover, these chemical cues can be delivered either at the whole cell or subcellular level. (iv) Microfluidic devices offer the possibility of measuring the intrinsic mechanical properties of cells in a high throughput fashion. (v) Finally, microfluidic methods provide exquisite control over drop size, generation, and manipulation. As a result, droplets are being increasingly used to control the physicochemical environment of cells and as biomimetic analogs of living cells. These powerful attributes of microfluidics should further stimulate novel means of investigating the link between physicochemical cues and the biomechanical response of cells. Insights from such studies will have implications in areas such as drug delivery, medicine, tissue engineering, and biomedical diagnostics

Rheological Behavior of a Dispersion of Small Lipid Bilayer Vesicles

Rheological behavior of a dispersion of small nearly-unilamellar phospholipid bilayer vesicles has been investigated. We conducted steady-state shear experiments and linear viscoelastic experiments. In the dilute and semidilute regime the rheological behavior is similar to that of a hard-sphere dispersion as reported in the literature for viscoelastic measurements, but now also observed in steady shear experiments. The effect of the main acyl-chain phase transition, taking place at 23 °C, can be described with an increase of the effective volume fraction. As a result, with temperature variation one can obtain effective volume fractions larger than the maximum packing fraction for hard spheres. Near and above the maximum packing fraction a dynamic yield stress ty and a frequency independent storage modulus G' develop. In this concentration regime the rheological behavior is determined by the interplay between vesicle deformation and the intervesicle interaction, and so far, there is no indication which phenomenon is dominant. A comparison with recently reported measurements suggests that G' is proportional to a-3, where a is the vesicle radius. Furthermore, we show that ty = γcG' which is in agreement with theory. Here tγ is the dynamic yield stress and γc the critical strain which indicates the transition to nonlinear behavior in a viscoelastic experiment. There is a striking resemblance between our high concentration results and those reported in literature for vesicles in the so-called onion phase. To the best of our knowledge this is the first rheological study for concentrated nearly-unilamellar vesicle dispersions with volume fraction and temperature as variables

Electrowetting of complex fluids: perspectives for rheometry on chip

We explore the possibilities of electrowetting (EW) as a tool to assess the elastic properties of aqueous jellifying materials present in the form of a small droplet on a hydrophobic substrate. We monitored the EW response of aqueous solutions of gelatin (2−10 wt %) in ambient oil for various temperatures (8−40 °C) below and above the gel point. Whereas the drops remained approximately spherical cap-shaped under all conditions, the voltage-induced reduction of the contact angle became progressively less pronounced upon entering the gel state at lower temperatures. We modeled the decrease in contact angle by minimizing the total energy of the drops consisting of interfacial energies, electrostatic energy, and the elastic energy due to the deformation of the drop, which was taken into account in a modified Hertz model. This allowed fitting the data and extracting the elastic modulus G, which were found to agree well with macroscopic storage moduli G′ obtained with oscillatory shear rheometry. These results show that EW can be used as a tool for characterizing soft materials with the elastic moduli ranging (at least) from 10 to 1000 Pa. Our observations also create interesting perspectives for performing in situ rheological measurement inside microfluidic chips