Ultrasonic interferometry: study of particle sedimentation in liquid.

An ultrasonic interferometry method was designed to study sedimentation of particles in liquid. The method, based on A mode echography, measures the amplitude of ultrasonic waves reflected (echo E1) by a fixed interface I1 called "solid plate-sediment" interface formed when particles are sedimenting on a solid plate. The amplitude of the echo depends both on mechanical properties of the three media (solid plate, sediment and suspension) on the thickness of the sediment and on the presence of a second mobile interface I2 called "sediment-suspension" interface. In the first phase of sedimentation when the second interface is very close to the first, two reflected waves interfere. Then, in the second phase of sedimentation when the sediment is thick enough, the amplitude of the echo E1 depends only on the sediment and solid plate properties. The first phase will give information on the sedimentation rate of particles (SR). We have compared SR of particles determined by this method with SR measured in a cylindrical tube of the same geometry as the ultrasonic measurement cell and with theoretical values of the sedimentation rate given by theoretical models.

Determination of erythrocyte transit times through micropores. I--Basic operational principles.

To study the transit times of each red blood cell passing through cylindrical micropores and in order to evaluate sub-population of cells with regard to their deformability, we have developed a new system called the cell transit time analyser (CTTA). By using an AC voltage (100 KHz) across a special filter, we measure the electrical conductance change produced by the cells passing through the pores under a known driving pressure. This computer based device provides the distribution of transit times tau for 2000 cells in 1 minute and as a result the mean transit time [tau]. Experiments with red cells were designed to evaluate the flow behavior of both normal cells and cells whose mechanical properties were artificially altered. Cell volume was changed by use of non-isotonic media. Cell shape and cell volume were modified by varying the pH of the suspending buffer. Results of these experiments are: 1) a skew distribution of transit times towards high tau values for both control cells and artificially altered cells is observed: 2) [tau] is minimum for isotonic conditions and increases sharply for either hypotonic or hypertonic media: 3) [tau] is minimum at physiological pH and increases for either acid or alcaline changes of pH.