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Biomedical subjects

Stefan Bernet

Publications and source records attributed to Stefan Bernet.

5 recordsLinked to original sources

Spiral interferogram analysis.

Interference microscopy using spatial Fourier filtering with a vortex phase element leads to interference fringes that are spirals rather than closed rings. Depressions and elevations in the optical thickness of the sample can be distinguished immediately by the sense of rotation of the spirals. This property allows an unambiguous reconstruction of the object's phase profile from one single interferogram. We investigate the theoretical background of "spiral interferometry" and suggest various demodulation techniques based on the processing of one single interferogram or multiple interferograms.

Journal Article↗

Spiral interferometry.

We present a surprising modification of optical interferometry. A so-called spiral phase element in the beam path of a standard microscope results in an interferogram of phase samples, for which the interference fringes have the shape of spirals instead of closed contour lines as in traditional interferograms. This configuration overrides the basic problem of interferometry, i.e., that elevations and depressions cannot be distinguished. Therefore a complete sample profile can be reconstructed from a single exposure, promising, e.g., high-speed metrology with a single laser pulse. The method is easy to implement, it does not require a spatially separated reference beam, and it is optimally stable against environmental noise.

Journal Article↗

Shadow effects in spiral phase contrast microscopy.

Recently it has been demonstrated that spatial filtering of images in microscopy with a spiral phase element in a Fourier plane of the optical path results in a strong edge enhancement of object structures. In principle the operation is isotropic, i.e., all phase edges of a sample object are highlighted simultaneously, independent of their local direction. However, here we demonstrate that the symmetry can be broken intentionally by controlling the phase of the central area of a spiral phase hologram, which is displayed at a computer controlled spatial light modulator. This produces an apparent shadow effect which can be rotated at video rate. The resulting relieflike impression of the sample topography with a longitudinal resolution in the subwavelength regime is demonstrated by imaging a standard low contrast test sample consisting of a human cheek cell.

Journal Article↗

[Spatial and temporal control of ultrasonic fields via optoacoustic holography].

The present paper presents a new method for generating ultrasound, based on the interaction of laser-induced ultrasound generation and ultrasonic holography. An ultrasonic field generated in a water tank via the optoacoustic effect is spatially and temporally controlled: In order to produce defined ultrasonic frequencies in the MHz range, the laser pulses incident on a light-absorbing layer are modulated in time using an electro-optic modulator (EOM). Additionally, a high-resolution liquid crystal spatial light modulator (SLM) is used to imprint a pre-calculated phase front to the laser beam. A computer-generated binary hologram is also displayed at the SLM. The expanded laser beam projects the corresponding pattern to the plane absorptive layer in the water tank. The projection of specific patterns for the generation of ultrasonic beams resembles the use of, diffractive optical elements" in optics. Optical ultrasound generation with holographic steering is a flexible tool with promising numerous new applications in medical and technical ultrasound diagnostics.

Dose-Response Relationship, Radiation↗

Mechanical forces impeding exocytotic surfactant release revealed by optical tweezers.

The release of surfactant from alveolar type II cells is essential to lower the surface tension in the lung and to facilitate inspiration. However, the factors controlling dispersal and diffusion of this hydrophobic material are still poorly understood. Here we report that release of surfactant from the fused vesicle, termed lamellar body (LB), resisted mechanical forces applied by optical tweezers: At constant trapping force, the probability to expand LB contents, i.e., to "pull" surfactant into the extracellular fluid, increased with time after LB fusion with the plasma membrane, consistent with slow fusion pore expansion in these cells. Elevations of the cytoplasmic Ca(2+) concentration ([Ca(2+)](c)) had a similar effect. Inasmuch as surfactant did not disintegrate in the extracellular space, this method permitted for the first time the determination of elastic and recoil properties of the macromolecular complex, yielding a spring constant of approximately 12.5 pN/ micro m. This is the first functional evidence that release of hydrophobic material is mechanically impeded and occurs in an "all-or-none" fashion. This mode of release is most probably the result of cohesive forces of surfactant, combined with adhesive forces and/or retaining forces exerted by a constrictive fusion pore acting as a regulated mechanical barrier, withstanding forces up to 160 pN. In independent experiments equiaxial strain was exerted on cells without optical tweezers. Strain facilitated surfactant release from preexisting fused vesicles, consistent with the view of mechanical impediments during the release process, which can be overcome by cell strain.

Animals↗