We present a digital holographic microscope that permits one to image polarization state. This technique results from the coupling of digital holographic microscopy and polarization digital holography. The interference between two orthogonally polarized reference waves and the wave transmitted by a microscopic sample, magnified by a microscope objective, is recorded on a CCD camera. The off-axis geometry permits one to reconstruct separately from this single hologram two wavefronts that are used to image the object-wave Jones vector. We applied this technique to image the birefringence of a bent fiber. To evaluate the precision of the phase-difference measurement, the birefringence induced by internal stress in an optical fiber is measured and compared to the birefringence profile captured by a standard method, which had been developed to obtain high-resolution birefringence profiles of optical fibers.
Optical low-coherence ref lectometry is applied for the first time to our knowledge to investigate diffusive biological tissues with a single-mode fiber probe. Samples of fresh arteries are studied, using the backscattered light from the tissue. The probed volume in the vicinity of the fiber tip is estimated to be below 6.7 x 10(-10) cm(3). This noninvasive method allows one to determine optical parameters, such as the index of refraction and the transmission properties, and the tissue thickness.
An array of high numerical aperture parabolic micromirrors (NA = 0.96) is used to generate multiple optical tweezers and to trap micron-sized dielectric particles in three dimensions within a fluidic device. The array of micromirrors allows generating arbitrarily large numbers of 3D traps, since the whole trapping area is not restricted by the field-of-view of the high-NA microscope objectives used in traditional tweezers arrangements. Trapping efficiencies of Q max r 0.22, comparable to those of conventional tweezers, have been measured. Moreover, individual fluorescence light from all the trapped particles can be collected simultaneously with the high-NA of the micromirrors. This is demonstrated experimentally by capturing more than 100 fluorescent micro-beads in a fluidic environment. Micromirrors may easily be integrated in microfluidic devices, offering a simple and very efficient solution for miniaturized optical traps in lab-on-a-chip devices.
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