We report on the use of standing surface acoustic waves, formed on a single-crystal piezoelectric substrate, to organize micron-scale latex particles into an array comprising a series of lines in an adjacent microfluidic system. The lines of particles are formed parallel to the substrate surface and perpendicular to the surface acoustic wave vector. They extend across the width of the acoustic beam aperture, with a periodicity of one-half the surface acoustic wavelength. The position and spacing of the particle arrays can be altered by adjusting the acoustic wave frequency within the device passband. We discuss the mechanism responsible for the formation of the lines, which could be widely applicable to the alignment of microscopic objects held in suspension.

We demonstrate the directed control of charge carriers in graphene using the electric field that accompanies the propagation of surface acoustic waves (SAWs) on a piezoelectric surface. Graphene grown by chemical vapor deposition was transferred to the surface of lithium niobate, allowing its direct integration with interdigital transducers used for SAW generation and detection. Radio frequency (RF) signal applied to the transducers at their resonant frequency was found to generate a direct current flow by the transport of p-type charge carriers. The acoustically induced current scales linearly with the applied RF power and can be observed even in presence of a counter-flow current induced by an applied bias.

Development of bioadhesive formulations for tissue fixation remains a challenge. The major drawbacks of available bioadhesives are low adhesion strength, toxic byproducts, and complexity of application onto affected tissues. In order to address these problems, this study has developed a hydrogel bioadhesive system based on poly amido amine (PAMAM) dendrimer, grafted (conjugated) with UV-sensitive, 4-[3-(trifluoromethyl)-3H-diazirin-3-yl] benzyl bromide (PAMAM-g-diazirine). This particular diazirine molecule can be grafted to the surface amine groups of PAMAM in a one-pot synthesis. Diazirine functionalities are carbene precursors that form covalent crosslinks with hydrated tissues after low-power UV activation without necessity of free-radical initiators. The rheological properties and adhesion strength to ex vivo tissues are highly controllable depending on diazirine grafting, hydrogel concentration, and UV dose intensity fitting variety types of tissues. Covalent bonds at the tissue/bioadhesive interface provide robust adhesive and mechanical strength in a highly hydrated environment. The free flowing hydrogel conversion to elastic adhesive after UV activation allows intimate contact with the ex vivo swine tissue surfaces with low in vitro cytotoxicity observed, making it a promising bioadhesive formulation toward clinical applications.

The two-dimensional concentration and manipulation of micron-scale particles by orthogonal, surface acoustic, standing waves is demonstrated. The particles are organized by liquid pressure waves in a microfluidic system over a piezoelectric substrate and form a uniform two-dimensional array with a spacing governed by the mechanical nodes of the two orthogonal, surface acoustic, standing waves. The nodal spacing can be controlled in each orthogonal direction independently by adjustment of the radio frequency applied to the separate acoustic wave transducers. This technique could be used to enhance the particle concentrations at sensing locations in DNA or protein array detectors.

Soft tissue fixation of implant and bioelectrodes relies on mechanical means (e.g. sutures, staples, screws), with associated complications of tissue perforation, scarring, and interfacial stress concentrations. Adhesive bioelectrodes address these shortcomings with voltage cured carbene-based bioadhesives, locally energized through graphene interdigitated electrodes.Electro-rheometry and adhesion structure activity relationships were explored with respect to voltage and electrolyte on bioelectrodes synthesized from graphene 3D-printed onto resorbable polyester substrates. Adhesive leachates effects on in vitro metabolism and human derived platelet rich plasma response serves to qualitatively assess biological response. The voltage activated bioadhesives are found to have gelation times of 60 sec or less with maximum shear storage modulus (G') of 3 kPa. Shear modulus mimics reported values for human soft tissues (0.1-10 kPa). The maximum adhesion strength achieved for the ~50 mg bioelectrode films is 170 g cm -2 (17 kPa), which exceeds the force required for tethering of electrodes on dynamic soft tissues. The method provides the groundwork for implantable bio/electrodes that may be permanently incorporated into soft tissues, vis-à-vis graphene backscattering wireless electronics since all components are bioresorbable.

Acoustic fields have been widely used for manipulation of particles and cells within microfluidic systems. In this Letter, we explore a novel acoustofluidic phenomenon for particle patterning and focusing, where a periodic acoustic pressure field is produced parallel to internal channel boundaries with the imposition of either a traveling or standing surface acoustic wave (SAW). This effect results from the propagation and intersection of edge waves from the channel walls according to the Huygens-Fresnel principle and classical wave fronts from the substrate-fluid interface. We demonstrate versatile control over this effect to produce both one- and two-dimensional acoustic patterning from one-dimensional SAW fields and its utility for continuous particle focusing. Uniquely, this channel-guided acoustic focusing permits the generation of robust acoustic fields without channel resonance conditions and particle focusing positions that are difficult or impossible to produce otherwise.

Acoustic waves can be used to accurately position cells and particles and are appropriate for this activity owing to their biocompatibility and ability to generate microscale force gradients. Such fields, however, typically take the form of only periodic one or two-dimensional grids, limiting the scope of patterning activities that can be performed. Recent work has demonstrated that the interaction between microfluidic channel walls and travelling surface acoustic waves can generate spatially variable acoustic fields, opening the possibility that the channel geometry can be used to control the pressure field that develops. In this work we utilize this approach to create novel acoustic fields. Designing the channel that results in a desired acoustic field, however, is a non-trivial task. To rapidly generate designed acoustic fields from microchannel elements we utilize a deep learning approach based on a deep neural network (DNN) that is trained on images of pre-solved acoustic fields. We use then this trained DNN to create novel microchannel architectures for designed microparticle patterning. Microfluidic platforms are an important tool for precise micromanipulation, using force gradients on the length scale of cells and microparticles themselves. A major application space in microfluidics is the patterning and long-term retention of living cells; patterning is a powerful tool for the formation of cellular spheroids 1 , tissue engineering 2 , drug screening 1 and single-cell analysis 3 , cellular interactions 4 , and mechanobiology 5. The design of microfluidic systems for these activities, however, typically occurs on a first-principles basis and generally omits parametric optimization of the microchannel features. This has a large impact when hydrodynamic forces are involved, since the channel geometry can affect how, for example, lift and drag forces are distributed. In the case of hydrodynamic effects there has been some work using numerical simulations 6,7 to configure channels to optimize their mixing and dilution characteristics, showing the promise of modifying channel shapes for creating optimized microfluidic devices. Actively applied forces, rather than just hydrodynamic ones, however, are increasingly integrated into microfluidic devices for more refined and dynamic actuation. Acoustic fields are a particularly useful method for micromanipulation due to their biocompatibility, high force magnitudes arising from MPa order pressures and wavelengths that can match the length scale of individual cells. To date, acoustic fields have shown their capacity for versatile microscale actuation activities including patterning 8 , acoustic streaming 9-11 , droplet manipulation 12 , cell cultures 13,14 , mixing 15,16 and sorting 8 , with actuation down to the single cell level 12,17. In the case of patterning, these fields have typically been limited to creating simple lines 18 or grids 19 of cells and microparticles due to the limitations imposed by the transducers and channel geometries. For the most part these ...

The invasive practice of suturing for wound closure has persisted for millennia; with the rate of medical development, it is staggering that there are few viable alternatives to invasive mechanical fasteners. Biocompatible and biodegradable polymers are attractive candidates for versatile bioadhesives and could revolutionize surgical procedures. Bioadhesives can be broadly placed into two groups: activated and instant. Almost all commercially available bioadhesives are instant, which cross-link by mixing two components or on contact with moisture. Activated bioadhesives, on the other hand, allow control of when and where a bioadhesive cross-links and, in some cases, the extent of cross-linking. Despite significant progress, there has been little translation of activated bioadhesives to clinical use. This review discusses recent developments in UV-activated bioadhesives toward addressing unmet clinical needs.