This paper presents a micro-flow diagnostic technique, 'high-speed confocal micro-particle image velocimetry (PIV)', and its application to the internal flow measurement of a droplet passing through a microchannel. A confocal micro-PIV system has been successfully constructed wherein a high-speed confocal scanner is combined with the conventional micro-PIV technique. The confocal micro-PIV system enables us to obtain a sequence of sharp and high-contrast cross-sectional particle images at 2000 frames s(-1). This study investigates the confocal depth, which is a significant parameter to determine the out-of-plane measurement resolution in confocal micro-PIV. Using the present confocal micro-PIV system, we can measure velocity distributions of micro-flows in a 228 microm x 171 microm region with a confocal depth of 1.88 microm. We also propose a three-dimensional velocity measurement method based on the confocal micro-PIV and the equation of continuity. This method enables us to measure three velocity components in a three-dimensional domain of micro flows. The confocal micro-PIV system is applied to the internal flow measurement of a droplet. We have measured three-dimensional distributions of three-component velocities of a droplet traveling in a 100 microm (width) x 58 microm (depth) channel. A volumetric velocity distribution inside a droplet is obtained by the confocal micro-PIV and the three-dimensional flow structure inside the droplet is investigated. The measurement results suggest that a three-dimensional and complex circulating flow is formed inside the droplet.

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The study deals with a microfluidic method to investigate the transient behavior of microcapsules in flow. The technique consists of investigating ovalbumin microcapsules passing through a convergent-divergent microchannel made of PolyDiMethylSiloxane. We work with three types of square microchannel with, respectively, cross section values of h 9 h = 30 9 30, 50 9 50 and 70 9 70 lm. The microchannels length is L = 3h. We analyze the kinetics of deformation of the microcapsules in the microchannels for velocity ranging from 2 to 5 cm/s and for microcapsule size ratio d/h ranging from 0.9 to 2.5. The relaxation process at the pore outlet is modeled using an exponential relaxation law. We show that that the relaxation time at the divergent outlet depends on the microcapsule size ratio d/h. Thanks to the analytical expression of the relaxation, we extract a shear modulus of the membrane equal to 0.04 N/m. This value is consistent with the value of 0.07 N/m that we found using the steady state analysis performed in cylindrical glass capillaries. Thus, it is interesting to notice that the microcapsule behavior based on a simple analytical model can be successfully described despite the complex flow situation consisting of deformable microcapsule in confined square microchannels.

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The development of an in vitro functional liver zonation model is a major issue to reproduce physiological liver features. Oxygen concentration is one of the potential explanations of a primary regulating factor of zonation. In this frame, we investigated the oxygen gradient inside a microfluidic device containing rat hepatocyte cultures. The device integrated a platinum (Pt) (II) octaethylporphyrin sensor, allowing a 2D mapping of the oxygen concentration. After 3 hr adhesion of the hepatocytes, the sensor indicated an intense oxygen depletion, leading to an oxygen shortage in the center of the device. After a 30 min perfusion of the culture medium, we monitored the formation of the oxygen gradient along the culture due to cellular respiration. The profile of the oxygen gradient was modulated and controlled by increasing either the perfusion flow rate or the device thickness. In addition, the oxygen gradient was time dependent as far as it decreased with the time of culture. Perivenous and periportal liver patterns were characterized by the immunostaining of the hepatic markers. We put in evidence a spatio temporal hepatic organization. We observed the overexpression since 24 hr of perfusion of the APC and PCK1 proteins upstream in the oxygen‐rich area of the device. The overexpression of GS, GCK, CYP1A, and HIFα proteins were observed downstream in the oxygen‐poor area. Then, CYP3A2 and β‐catenin spatial reorganization was achieved after 48 hr of culture. The results presented a partial zonation‐like pattern that was superimposed with an oxygen gradient profile.