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Electroosmotic flow (EOF) in microchannels is restricted to low Reynolds number regimes. Since the inertial forces are extremely weak in such regimes, turbulent conditions do not readily develop. Therefore, species mixing occurs primarily via diffusion, with the result that extended mixing channels are generally required. The present study considers a T-shaped microchannel configuration with a mixing channel of width W=280 µm. Computational fluid dynamics simulations and experiments were performed to investigate the influence on the mixing efficiency of various geometrical parameters, including the side-channel width, the side-channel separation, and the number of side-channel pairs. The influence of different applied voltages is also considered. The numerical results reveal that the mixing efficiency can be enhanced to yield a fourfold improvement by incorporating two pairs of side channels into the mixing channel. It was also found that the mixing performance depends significantly upon the magnitudes of the applied voltages.

Differentiating between early malignancy and benign lesions in oral cavities is difficult using current optical tools. As has been shown in previous studies, microvascular changes in squamous epithelium can be regarded as a key marker for diagnosis. We propose the combination of structural and vascular optical coherence tomography (OCT) imaging for the investigation of disease related changes. Progressive thickness changes of epithelium and the destruction of underlying lamina propria was observed during cancer development in a 4- nitroquinoline-1-oxide (4NQO) mouse model. At the same time, microvascular changes in hyperplasia, dysplasia, carcinoma in situ and advanced cancer were observed. Findings from OCT imaging were compared with histology.

This paper presents a T-form electrokinetic injection system for the discrete time-based loading and dispensing of samples of variable-volume in a microfluidic chip. A novel push-pull effect is produced during the loading and dispensing processes by the application of an appropriate control voltage distribution. The experimental and numerical results show that this push-pull loading technique produces compact sample plugs and hence improves the detection resolution of the microfluidic device. The injection system is integrated with a microflow switch, and a suitable voltage control scheme is proposed to guide the sample to the desired outlet port such that the microfluidic device can function as a microdispenser. The time-based variable-volume T-form injection method presented in this study is performed using a compact geometry and a simple control scheme and can be readily integrated with other microfluidic devices to form a microfluidic system capable of continuous monitoring and analysis of bioreactions in the life science and biochemistry fields.

This paper presents a novel technique for manipulating fluid flows within microchannels using bare electrodes. The electrodes, with a width of 100 lm, are fabricated using conventional photolithography techniques by etching the bulk flow channel into a glass substrate and then depositing Pt/Cr thin films within this channel. The application of an external voltage to these electrodes produces localized variations in the electrical potential distribution, which in turn induce changes in the velocity and direction of the flow within the microchannel. The effectiveness of the proposed control technique is investigated numerically using computational fluid dynamics simulations and experimentally using a fabricated microchip containing multiple bare electrode-pairs. The results demonstrate that the application of appropriate driving voltages to the bare electrode-pairs enables the microdevice to function as a nozzle, a diffuser, a mixer or a valveless valve.