Artificial ommatidia by self-aligned microlenses and waveguides.

We report the fabrication of artificial ommatidia, the imaging units of insects' compound eyes, by use of polymer integrated optics. These biomimetic structures are obtained by configuring microlenses to play dual roles for self-writing of waveguides (during the fabrication) and collection of light (during the operation). The artificial ommatidium, consisting of a microlens, a spacer, and a waveguide, directly resembles the structure of its biological counterpart.

Biomimetic technique for adhesion-based collection and separation of cells in a microfluidic channel.

A basic step in many biological assays is separating and isolating different types of cells from raw samples. To better meet these requirements in microfluidic devices for miniature biomedical analytical systems, an alternative method for separating cells has been devised by mimicking the physiological process of leukocyte recruitment to blood vessel walls: adhesive cell rolling and transient tethering. Reproducing these interactions for cells on surfaces of microstructured fluidic channels can serve to capture and concentrate cells and even to fractionate different cell types from a continuously flowing sample.

A novel high aspect ratio microfluidic design to provide a stable and uniform microenvironment for cell growth in a high throughput mammalian cell culture array.

We present a high aspect ratio microfluidic device for culturing cells inside an array of microchambers with continuous perfusion of medium. The device was designed to provide a potential tool for cost-effective and automated cell culture. The single unit of the array consists of a circular microfluidic chamber 40 microm in height surrounded by multiple narrow perfusion channels 2 microm in height.

A single cell electroporation chip.

Increasing the cell membrane's permeability can be accomplished via single cell electroporation. Polar substances that cannot otherwise permeate the plasma membrane (such as dyes, drugs, DNA, proteins, peptides, and amino acids) can thus be introduced into the cell. We developed a polymeric chip that can selectively immobilize and locally electroporate single cells.

Theoretical and experimental study towards a nanogap dielectric biosensor.

Theoretical and experimental studies of nanogap capacitors as potential label free biosensors are presented. The nanogap device is capable of detecting the existence of single stranded DNA (ssDNA) oligonucleotides (20-mer) in 100 nM aqueous solutions using a 20 nm gap of 1.2 pl in volume.

Continuous perfusion microfluidic cell culture array for high-throughput cell-based assays.

We present for the first time a microfluidic cell culture array for long-term cellular monitoring. The 10 x 10 array could potentially assay 100 different cell-based experiments in parallel. The device was designed to integrate the processes used in typical cell culture experiments on a single self-contained microfluidic system.

Role of cell surface heparan sulfate proteoglycans in endothelial cell migration and mechanotransduction.

Endothelial cell (EC) migration is critical in wound healing and angiogenesis. Fluid shear stress due to blood flow plays an important role in EC migration. However, the role of EC surface heparan sulfate proteoglycans (HSPGs) in EC adhesion, migration, and mechanotransduction is not well understood.

Tunable microdoublet lens array.

We report a tunable microdoublet lens capable of creating dual modes of biconvex or meniscus lens. The microdoublet lens consists of a tunable liquid-filled lens and a solid negative lens. It can be tuned either by changing the shape of the liquid-filled lens into bi-convex or meniscus or by changing a filling media with different refractive index.

Micromachined transmissive scanning confocal microscope.

We have developed a miniature scanning confocal microscope that uses electrostatically actuated microlenses for focusing and scanning. Objective lenses, scanners, a pupil, and a pinhole of the confocal microscope are microfabricated and integrated into a volume smaller than 2 mm3 by stacking these components. Objective lenses are composed of two vertically cascaded polymer microlenses integrated into micromachined comb actuators.

Total internal reflection-based biochip utilizing a polymer-filled cavity with a micromirror sidewall.

A total internal reflection (TIR)-based biochip utilizing a polymer-filled cavity with a micromirror sidewall has been designed and fabricated. The implementation of the micromirror sidewall cavity facilitates precise alignment of the excitation light beam into the system. The incident angle of illumination can be easily modified by selecting polymers of different indices of refraction while optical losses are minimized.

Reagentless mechanical cell lysis by nanoscale barbs in microchannels for sample preparation.

A highly effective, reagentless, mechanical cell lysis device integrated in microfluidic channels is reported. Sample preparation, specifically cell lysis, is a critical element in 'lab-on-chip' applications. However, traditional methods of cell lysis require purification steps or complicated fabrication steps that a simple mechanical method of lysis may avoid.

Effects of flavonoid-rich beverages on prostacyclin synthesis in humans and human aortic endothelial cells: association with ex vivo platelet function.

Diets rich in flavonoids have been associated with reduced risk for cardiovascular disease. This may be due, in part, to flavonoid-induced alterations in eicosanoid synthesis. Our objective was to identify plant-derived beverages that alter synthesis of prostacyclin in cultured human aortic endothelial cells (HAEC), and to determine if these beverages could alter in vivo 6-keto-prostaglandin F(1alpha) (a stable metabolite of prostacyclin) synthesis and platelet function.

Tunable liquid-filled microlens array integrated with microfluidic network.

An elastomer-based tunable liquid-filled microlens array integrated on top of a microfluidic network is fabricated using soft lithographic techniques. The simultaneous control of the focal length of all the microlenses composing the elastomeric array is accomplished by pneumatically regulating the pressure of the microfluidic network. A focal length tuning range of hundreds of microns to several millimeters is achieved.