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Biomedical subjects

E Glossner

Publications and source records attributed to E Glossner.

7 recordsLinked to original sources
PubMed1994

The Macro Flow Planktometer: a new device for volume and fluorescence analysis of macro plankton including triggered video imaging in flow.

A newly developed macro flow planktometer is described for measuring plankton organisms with a size of 100-2,000 microns by the flow principle in time-saving and noncontact fashion. Based on the method of changes in electric resistance (Coulter principle), the device allows determination of the body volume of living organisms in their natural medium (fresh or seawater) at a measuring rate of up to 50 organisms per second. Simultaneous, laser-excited fluorescence measurement permits quantitative detection of fluorescent substances within the organisms. Controlled by the multiparametric measurement, video images of organisms of particular interest can be taken in the flow chamber using a stroboscopic imaging system. Valuable morphological information on the material under test is thus available in addition to the analytical measurement. Data acquisition and imaging, the total system control, and the fast data evaluation are performed with an IBM-AT compatible computer using an extensive software package. The easy-to-handle desktop unit can be used both in land laboratories and on ships. The modular structure of the system permits any desired combination of individual components to adapt it to various requirements. The operability of this new measuring system is demonstrated by several applications.

Animals↗
PubMed1979

Fast imaging in flow: a means of combining flow-cytometry and image analysis.

The morphological identification of cells by flow cytometry is difficult. Usually cell sorting and microscopical analysis have to be used in addition. Morphological analysis is simplified by taking cell pictures from a range of particular interest immediately during flow cytometric analysis. Instruments using the video scanning technique for fluorescence imaging are slow and expensive (8, 10). Morphological information can also be obtained by transmission imaging of cells in flow, which requires shorter exposure times. Therefore a cell volume activated flow imaging device has been developed which operates at flow speeds up to 5 m/sec and which depicts transmission images of selected cells on a 16-mm film by a nsec flashlamp illumination. An electronic unit detects the particles in the optically accessible orifice, performs the pulse height analysis, triggers the flashlamp if particles are in the preselcted range of interest and feeds the film. The instrument is capable of delivering up to 150 pictures per second and works either as a flow microscope in which the cells in the preselected volume range are directly observed, or as a picture system in which the cell pictures are stored on the 16-mm film for documentation or for image analysis.

Cell Count↗
PubMed1977

Uniform lateral orientation, caused by flow forces, of flat particles in flow-through systems.

Recently, it was shown that the lateral orientation of sperm cells disturbs the deoxyribonucleic acid distribution measured by fluorescence in a laterally laser-illuminated flow system. The present results show how flat particles may be influenced to assume a uniform lateral orientation. This was achieved by choosing the geometrical dimensions of the hydrodynamic focusing flow path. High speed photographs of fixed chicken erythrocytes oriented in experimental chambers are presented.

Animals↗
PubMed1977

Fluvo-metricell, a combined cell volume and cell fluorescence analyzer.

A new flow through instrument that simultaneously measures cell volume (resistance pulse technique) and cell fluorescence in the same orifice will be described. The fluorescence pulses of the hydrodynamically focussed cells are picked up by the optics via the axial direction (principle of Dittrich and Goehde, Z Naturforsch 24b:360, 1969). There is no coordination problem between the fluorescence and the resistance pulses to be observed because a new type of transducer is used. The electronic system provides gating of one or two parameter histograms. Function tests are performed with the incorporated two-parameter test spectrum generator. Different examples of using the instrument in practice are shown. The volume that may be measured with an orifice of 70 micron diameter ranges between 4 and 1400 micron3 (1:350). Coefficients of variation of the fluorescence below 2% are measured.

Cytological Techniques↗
PubMedDate not supplied

A PC-at based video device for flow cytometrically triggered cell imaging in flow.

A personal computer-based system of imaging in flow is described which takes cell images directly from the transducer of a flow cytometer. Imaging is triggered by the pulses of the flow system. The movement of the cells is frozen by ultra-short flashes from pulsed light emitting diodes (LED). The images are taken up by a video camera, transferred to an add-in board of the PC and then stored on disk. A novel method has been developed for capturing the video images which normally arise in asynchronism with the video frame. Images of different cells and particles exposed during flow analysis are shown.

Computer Systems↗