Electric field-mediated adhesive dynamics of cells inside bio-functionalised microchannels offers important cues for active control of cell-substrate adhesion.

Adhesive dynamics of cells plays a critical role in determining different biophysical processes orchestrating health and disease in living systems. While the rolling of cells on functionalised substrates having similarity with biophysical pathways appears to be extensively discussed in the literature, the effect of an external stimulus in the form of an electric field on the same remains underemphasized. Here, we bring out the interplay of fluid shear and electric field on the rolling dynamics of adhesive cells in biofunctionalised micro-confinements. Our experimental results portray that an electric field, even restricted to low strengths within the physiologically relevant regimes, can significantly influence the cell adhesion dynamics. We quantify the electric field-mediated adhesive dynamics of the cells in terms of two key parameters, namely, the voltage-altered rolling velocity and the frequency of adhesion. The effect of the directionality of the electric field with respect to the flow direction is also analysed by studying cellular migration with electrical effects acting both along and against the flow. Our experiment, on one hand, demonstrates the importance of collagen functionalisation in the adhesive dynamics of cells through micro channels, while on the other hand, it reveals how the presence of an axial electric field can lead to significant alteration in the kinetic rate of bond breakage, thereby modifying the degree of cell-substrate adhesion and quantifying in terms of the adhesion frequency of the cells. Proceeding further forward, we offer a simple theoretical explanation towards deriving the kinetics of cellular bonding in the presence of an electric field, which corroborates favourably with our experimental outcome. These findings are likely to offer fundamental insights into the possibilities of local control of cellular adhesion via electric field mediated interactions, bearing critical implications in a wide variety of medical conditions ranging from wound healing to cancer metastasis.

Effect of skimming layer in an electroosmotically driven viscoelastic fluid flow over charge modulated walls.

We report a numerical study on the effect of the skimming layer in an EOF of Oldroyd-B fluid over charge modulated walls. Three types of flow conditions were identified on the basis of the relative thickness of the skimming layer and the electrical double layer. We observe maximum slip velocity magnitude when the skimming layer thickness is very less than the thickness of the electrical double layer. For higher skimming layer thickness compared to the thickness of electrical double layer, slip velocity magnitude attenuates, and the polymeric stress inside the skimming layer becomes zero. Enhanced fluid elasticity generates asymmetric flow structures inside the microchannel, which can also be achieved by imposing an asymmetric surface charge along the channel walls. Our present analysis highlights the complex flow dynamics of the EOF of biofluids/polymeric fluids with a near-wall region depleted of macro-molecules.

Electric-Field-Induced Pattern Formation in Layers of DNA Molecules at the Interface between Two Immiscible Liquids.

The concentration patterns of DNA molecules attached to the interface between two immiscible aqueous phases forming under an electric field are studied. The pattern formation is driven by hydrodynamic interactions between the molecules originating from the electro-osmotic flow due to the Debye layer around a molecule. A nonlinear integrodifferential equation is derived describing the time evolution of the concentration field at the liquid-liquid interface. A linear stability analysis of this equation shows that a mode of given wavelength is initially stable, but destabilizes after a critical time which is inversely proportional to the wavelength. The scaling behavior of the critical time with electric field strength and viscosity found in the experiments agrees with the predictions by the theoretical model.

Universality in coalescence of polymeric fluids.

A pendant drop merging with a sessile drop and subsequently forming a single daughter drop is known to exhibit complex topologies. But their dynamics are yet to be probed for fluids exhibiting characteristic relaxation time scales while undergoing the deformation process. Here, we unveil a universal temporal evolution of the neck radius of the daughter drop during the coalescence of two polymeric drops. Such a generalization does not rely on the existence of previously explored viscous and inertial dominated regimes for simpler fluids but is fundamentally premised on a unique topographical evolution with essential features of interest exclusively smaller than the dominant scales of the flow. Our findings are substantiated by a theoretical model that considers the drops under coalescence to be partially viscous and partially elastic in nature. These results are substantiated with high-speed imaging experiments on drops of polyacrylamide (PAM), polyvinyl alcohol (PVA), polyethylene oxide (PEO), and polyethylene glycol (PEG). The observations herein are expected to hold importance for a plethora of diverse processes ranging from biophysics and microfluidics to the processing of materials in a wide variety of industrial applications.

Electrical Power Generation from Wet Textile Mediated by Spontaneous Nanoscale Evaporation.

Developing low-weight, frugal, and sustainable power sources for resource-limited settings appears to be a challenging proposition for the advancement of next-generation sensing devices and beyond. Here, we report the use of centimeter-sized simple wet fabric pieces for electrical power generation by deploying the interplay of a spontaneously induced ionic motion across fabric nanopores due to capillary action and simultaneous water evaporation by drawing thermal energy from the ambient. Unlike other reported devices with similar functionalities, our arrangement does not necessitate any input mechanical energy or complex topographical structures to be embedded in the substrate. A single device is capable of generating a sustainable open circuit potential up to ∼700 mV, which is further scaled up to ∼12 V with small-scale multiplexing (i.e., deploying around 40 numbers of fabric channels simultaneously). The device is able to charge a commercial supercapacitor of ∼0.1 F which can power a white light-emitting diode for more than 1 h. This suffices in establishing an inherent capability of functionalizing self-powered electronic devices and also to be potentially harnessed for enhanced power generation with feasible up-scaling.

Capillary transport of two immiscible fluids in presence of electroviscous retardation.

The transport of two immiscible electrolytes through a narrow confinement whose walls bear a finite surface potential is analyzed through a lumped model by considering the influence of a regulatory self-induced axial electric field, termed as streaming potential. The presence of a surface charge on the channel walls culminates in the aqueous solutions carrying a net charge so as to make the overall system (channel and fluid) electrically neutral. The advection due to pressure driven flow or capillarity in the absence of any externally imposed electric field causes a preferential transport of net charged species. Thus, in order to render a net zero current through the system, there is an induced electric field which also retards the flow as a consequence of the force acting on the charged segments of fluid due to the streaming electric field. It is shown through a lumped model that for the situation of two distinct segments of fluids, the rate of front penetration into the capillary is strongly dependent on the relative conductivities of the two fluids. The streaming electric field evolves in accordance to the net conductivity of the channel and is responsible for dynamic changes in the retarding influence on the segments of fluid.

Electrokinetically modulated peristaltic transport of power-law fluids.

The electrokinetically modulated peristaltic transport of power-law fluids through a narrow confinement in the form of a deformable tube is investigated. The fluid is considered to be divided into two regions - a non-Newtonian core region (described by the power-law behavior) which is surrounded by a thin wall-adhering layer of Newtonian fluid. This division mimics the occurrence of a wall-adjacent cell-free skimming layer in blood samples typically handled in microfluidic transport. The pumping characteristics and the trapping of the fluid bolus are studied by considering the effect of fluid viscosities, power-law index and electroosmosis. It is found that the zero-flow pressure rise is strongly dependent on the relative viscosity ratio of the near-wall depleted fluid and the core fluid as well as on the power-law index. The effect of electroosmosis on the pressure rise is strongly manifested at lower occlusion values, thereby indicating its importance in transport modulation for weakly peristaltic flow. It is also established that the phenomenon of trapping may be controlled on-the-fly by tuning the magnitude of the electric field: the trapping vanishes as the magnitude of the electric field is increased. Similarly, the phenomenon of reflux is shown to disappear due to the action of the applied electric field. These findings may be applied for the modulation of pumping in bio-physical environments by means of external electric fields.

Streaming potential-modulated capillary filling dynamics of immiscible fluids.

The pressure driven transport of two immiscible electrolytes in a narrow channel with prescribed surface potential (zeta potential) is considered under the influence of a flow-induced electric field. The latter consideration is non-trivially and fundamentally different from the problem of electric field-driven motion (electroosmosis) of two immiscible electrolytes in a channel in a sense that in the former case, the genesis of the induced electric field, termed as streaming potential, is the advection of ions in the absence of any external electric field. As the flow occurs, one fluid displaces the other. Consequently, in cases where the conductivities of the two fluids differ, imbibition dynamically alters the net conductivity of the channel. We emphasize, through numerical simulations, that the alteration in the net conductivity has a significant impact on the contact line dynamics and the concomitant induced streaming potential. The results presented herein are expected to shed light on multiphase electrokinetics devices.

Electrokinetics in polyelectrolyte grafted nanofluidic channels modulated by the ion partitioning effect.

The effects of ion partitioning on the electrokinetics in a polyelectrolyte grafted nanochannel, which is the representative of a soft nanochannel, are analyzed. Earlier studies in this regard have considered low polyelectrolyte layer (PEL) grafting density at the rigid nanochannel wall and, hence, an equal permittivity inside and outside the grafted layer. In order to overcome this shortcoming, the concept of Born energy is revisited. The coupled system of the modified Poisson-Boltzmann and Navier-Stokes equation is solved numerically, going beyond the widely employed Debye-Hückel linearization and low PEL densities. The complex interplay between the hydrodynamics and charge distribution, modulated by the ion partitioning effect, along with their consequent effects on the streaming potential and electrokinetic energy conversion efficiency (EKEC) have been systemically investigated. It has been observed that the ion partitioning effect reduces the EKEC in comparison to the case with equal permittivity up to a certain electrical double layer thickness after which it increases the EKEC. For a high concentration of mobile charges within the PEL, the net gain in the maximum EKEC due to the ion partitioning effect is about 10 fold that of the case when the ion partitioning effect is not considered. We delve into the various scaling regimes in the streaming potential and intriguingly point out the exact location of peaks in efficiency. The present study also reveals the possibility of improvement in streaming potential mediated energy conversion by the use of polyelectrolyte materials, which possess substantially lower dielectric permittivity than the bulk electrolyte.

Consistent prediction of streaming potential in non-Newtonian fluids: the effect of solvent rheology and confinement on ionic conductivity.

By considering an ion moving inside an imaginary sphere filled with a power-law fluid, we bring out the implications of the fluid rheology and the influence of the proximity of the other ions towards evaluating the conduction current in an ionic solution. We show that the variation of the conductivity as a function of the ionic concentration is both qualitatively and quantitatively similar to that predicted by the Kohlrausch law. We then utilize this consideration for estimating streaming potentials developed across narrow fluidic confinements as a consequence of the transport of ions in a convective medium constituting a power-law fluid. These estimates turn out to be in sharp contrast to the classical estimates of streaming potential for non-Newtonian fluids, in which the effect of rheology of the solvent is merely considered to affect the advection current, disregarding its contributions to the conduction current. Our results have potential implications of devising a new paradigm of consistent estimation of streaming potentials for non-Newtonian fluids, with combined considerations of the confinement effect and fluid rheology in the theoretical calculations.

Ionic size dependent electroviscous effects in ion-selective nanopores.

Pressure-driven flows of aqueous ionic liquids are characterized by electroviscosity-an increase in the effective (apparent) viscosity because of an induced back electric field termed streaming potential. In this work, we investigate the electrokinetic phenomenon of streaming potential mediated flows in ion-selective nanopores. We report a dramatic augmentation in the effective viscosity as attributable to the finite size effect of the ionic species in counterion-only systems. The underlying physics involves complex interaction between the concerned electrochemical phenomena and hydrodynamic transport in a confined fluidic environment, which we capture through a modified continuum based approach and validate using molecular dynamics simulations. We obtain an expression for the ionic-size dependent streaming potential pertinent to the physical situation being addressed. The corresponding estimations of effective viscosity implicate that the classical paradigm of point sized ions can give rise to gross underestimations of the flow resistance in counterion-only systems especially for negligible surface (Stern layer) conductivity and large fluidic slip at the surface.

Pulsating electric field modulated contact line dynamics of immiscible binary systems in narrow confinements under an electrical double layer phenomenon.

We investigate the interfacial electro-chemical-hydrodynamics of an incompressible immiscible binary fluid system that moves in a narrow fluidic channel under time-periodic electroosmotic effects. We apply an alternating electrical voltage that sets the binary fluids in motion along the channel, whereas the channel walls are lined with chemical patch to alter the wetting characteristics of the surface. We demonstrate that the pulsating nature of the externally applied electric field in conjunction with the wetting characteristics of the surface may lead to some fascinating behavior of the contact line motion; which, in turn, may affect the capillary filling dynamics in an intriguing manner. Our results also unveil the profound influence of two important governing factors actuating the flow, namely, the frequency and amplitude of the time periodic electric field, on the tunability of the capillary filling rate and power requirement for filling the fluids into the channel.

Ionic size dependent electroosmosis in ion-selective microchannels and nanochannels.

Electrokinetics in salt-free media (in which counterions are only present) is central to the performance of many systems of modern technological relevance, ranging from ion-selective nanopores to electronic papers. Here, we introduce an analytical theory to describe the size dependence of electroosmosis in such typical scenarios, exhibiting an interesting confluence of the implications of interdependence of the electroosmotic transport mechanisms, ionic sizes, and confinement dimensions along with the counterion concentration. Our results do reveal that the concerned mobility parameter, describing the strength of electroosmotic transport, increases simultaneously with increments in the surface charge density as well as an ionic size factor (also known as the steric factor), bearing far-ranging consequences in microfluidic and nanofluidic technology.

Regimes of streaming potential in cylindrical nano-pores in presence of finite sized ions and charge induced thickening: an analytical approach.

We obtain approximate analytical expressions for the streaming potential and the effective viscosity in a pure pressure-driven flow through a cylindrical pore with electrokinetic interactions, duly accounting for the finite size effects of the ionic species (steric effects) and charge-induced thickening. Our analytical results show a remarkable agreement with the numerical solution even for high surface potentials and small channel radii. We demonstrate a consistent increment in the predicted value of the streaming potential and effective viscosity when finite size effects of the ionic species are accounted for. In addition to this, we account for the radial variation of in the viscosity of the fluid due to charge-induced thickening. We show that this so-called viscoelectric effect leads to a decrease in the induced streaming potential especially at high steric factors and high surface potentials. However, the viscoelectric effect, which is prominent at high zeta potential and narrow channels, does not cause significant changes in the electrokinetic conversion efficiency. These results shed light on the interesting confluence of the steric factor, the channel radius, the electrical double layer screening length, and the surface charge density in conjunction with the charge induced thickening, and thus provide ion-size dependent analytical framework for accurate system design and better interpretation of electrokinetic data.

Paper based microfluidic devices: a review of fabrication techniques and applications.

A wide range of applications are possible with paper-based analytical devices, which are low priced, easy to fabricate and operate, and require no specialized equipment. Paper-based microfluidics offers the design of miniaturized POC devices to be applied in the health, environment, food, and energy sector employing the ASSURED (Affordable, Sensitive, Specific, User-friendly, Rapid and Robust, Equipment free and Deliverable to end users) principle of WHO. Therefore, this field is growing very rapidly and ample research is being done. This review focuses on fabrication and detection techniques reported to date. Additionally, this review emphasises on the application of this technology in the area of medical diagnosis, energy generation, environmental monitoring, and food quality control. This review also presents the theoretical analysis of fluid flow in porous media for the efficient handling and control of fluids. The limitations of PAD have also been discussed with an emphasis to concern on the transformation of such devices from laboratory to the consumer.

Nucleic acid based point-of-care diagnostic technology for infectious disease detection using machine learning empowered smartphone-interfaced quantitative colorimetry.

We report a nucleic acid-based point of care testing technology for infectious disease detection at resource limited settings by integrating a low-cost portable device with machine learning-empowered quantitative colorimetric analytics that can be interfaced via a smartphone application. We substantiate our proposition by demonstrating the efficacy of this technology in detecting COVID-19 infection from human swab samples, using the RT-LAMP protocol. Comparison with gold standard results from real-time PCR evidences high sensitivity and specificity, ensuring simplicity, portability, and user-friendliness of the technology at the same time. Colorimetric analytics of the reaction output without necessitating the opening of the reaction microchambers enables execution of the complete test workflow without any laboratory control that may otherwise be required stringently for safeguarding against carryover contamination. Seamless sample-to-answer workflow and machine learning-based readout further assures minimal human intervention for the test readout, thus eliminating inevitable inaccuracies stemming from erroneous execution of the test as well as subjectivity in interpreting the outcome. Our results further indicate the possibilities of upgrading the technology to predict the pathogenic load on the infected patients akin to the cyclic threshold value of the real-time PCR, when calibrated with reference to a wide range of 'training' data for the machine learner, thereby putting forward the same as viable alternative to the resource-intensive PCR tests that cannot be made readily accessible at underserved community settings.

Combined effects of interfacial permittivity variations and finite ionic sizes on streaming potentials in nanochannels.

In this work, we investigate the effects of local permittivity variations, induced by a preferential orientation and exclusion of water dipoles close to channel walls, and the effects of finite-sized ions on the induced streaming potential in nanochannels. We make a detailed analysis of the underlying physicochemical interactions by considering combinations of cases where ions are considered to be point sized/finite sized and permittivity variation effects to be present/absent. By accounting for the dielectric friction (which in turn is a function of the local permittivity) in addition to the classical Stokes friction, we show that for high interfacial potentials and narrow confinements, the induced streaming potential field for the cases in which the polarization effects are considered for finite-sized ions is remarkably higher than for the cases in which the polarization effects are neglected. Thus, by coupling the nonlinear effects of finite-sized ions and water dipole polarization along with the dielectric friction, we open a new paradigm of streaming potential predictions for narrow fluidic confinements, bearing far-ranging scientific and technological consequences in nanoscale science and technology.

Smartphone-Integrated Label-Free Rapid Screening of Anemia from the Pattern Formed by One Drop of Blood on a Wet Paper Strip.

Screening of anemic patients poses demanding challenges in extreme point-of-care settings where the gold standard diagnostic technologies are not pragmatic and the alternative point-of-care technologies suffer from compromised accuracy, prohibitive cost, process complexity, or reagent stability issues. As a disruption to this paradigm, here, we report the development of a smartphone-based sensor for rapid screening of anemic patients by exploiting the patterns formed by a spreading drop of blood on a wet paper strip wherein blood attempts to displace a more viscous fluid, on the porous matrix of a paper, leading to "finger-like" projections at the interface. We analyze the topological features of the pattern via smartphone-enabled image analytics and map the same with the relative occupancy of the red blood cells in the blood sample, allowing for label-free screening and classification of blood samples corresponding to moderate to severe anemic conditions. The accuracy of detection is verified by comparing with gold standard reports of hematology analyzer, showing a strong correlation coefficient (R2) of 0.975. This technique is likely to provide a crucial decision-making tool that obviates delicate reagents and skilled technicians for supreme functionality in resource-limited settings.

Steric-effect induced alterations in streaming potential and energy transfer efficiency of non-newtonian fluids in narrow confinements.

In this work, we explore the possibilities of utilizing the combined consequences of interfacial electrokinetics and rheology toward augmenting the energy transfer efficiencies in narrow fluidic confinements. In particular, we consider the exploitation of steric effects (i.e., effect of finite size of the ionic species) in non-Newtonian fluids over small scales, to report dramatic augmentations in the streaming potential, for shear-thickening fluids. We first derive an expression for the streaming potential considering strong electrical double layer interactions in the confined flow passage and the consequences of the finite conductance of the Stern layer, going beyond the Debye-Hückel limit. With a detailed accounting for the excluded volume effects of the ionic species and their interaction with pertinent interfacial phenomena of special type of rheological fluids such as the power law fluids in the above-mentioned formalism, we demonstrate that a confluence of the steric interactions with the non-Newtonian transport characteristics may result in giant augmentations in the energy transfer efficiency for shear-thickening fluids under appropriate conditions.