Abstract: An image analysis system is used for the quantitation of nuclear proteins in cell populations. Particularly, the hormonal receptor content of fine needle aspirates of human breast carcinomas are evaluated. Estrogen or progesterone receptors are amplified and visualized in the specimen by a staining technique of the immunoperoxidase type. Monoclonal antibodies specific against the receptor are attached to the receptor sites and are then amplified by a bridging antibody which attaches to the monoclonal antibody and a peroxidase-antiperoxidase complex. A chromagen, diaminobenzidine is combined with the complex and treated with hydrogen peroxide to react with the peroxidase forming an insoluble brown precipitate which marks the receptor sites for optical identification. The specimen is then counterstained with another chromagen, methyl green which is specific to the nucleus of each cell.

Abstract: A method and apparatus is disclosed for use in performing automated classification of cells and other microscopic specimens. The apparatus provides a compact, adjustable assembly that is operable to provide: an operator-apparatus interactive classification system for the cell analysis; alternative techniques for different cells, cytoplasms and cell populations; and enchanced image or color separation and analysis.

Abstract: A kit for the quantitation of components in cell nuclei is described wherein the kit includes a stain and microscopic slides. Each slide has reference cell objects and a specimen cell area for receipt of specimen cells which are stained simultaneously with the reference cell objects.

Abstract: An image processing method and apparatus determines a proliferation index of a cell sample by staining the cells with a chromogen for a proliferation substance and a counterstain for the cell nuclei. The chromogen is activated by an antibody-enzyme conjugate which binds to the proliferation substance to produce a stained cell sample. The stained cell sample is examined with an optical microscope, forming a portion of the apparatus, which produces a magnified cell sample image. The apparatus optically filters the cell sample image and produces a pair of optically enhanced proliferation substance and cell nuclei images. The enhanced images are electronically analyzed to determine the amounts of cell nuclei and proliferation substance appearing in the images, respectively. The amounts are then compared to yield a proliferation index for the portion of the cell sample appearing in the cell sample image.

Abstract: An apparatus and method for staining cell objects on microscope slides includes a container for holding a staining solution and for holding one or more of the slides having the cell objects thereon. The container is preferably a Coplin jar in which is disposed a perforated cage containing a magnetic stirrer. Lower ends of the slides rest on the top of the cage and the stirrer drives liquid in and out of the cage and stirs and mixes the stain solution to obtain uniformity of stain concentration throughout the Coplin jar. A magnetic drive unit is positioned below the container and magnetic flux travels through the imperforated bottom wall of the glass Coplin jar to couple the stirrer rod to rotate within the cage, as the magnetic driver rotates in the unit beneath the jar.

Abstract: A method and apparatus are provided for selecting and analyzing a subpopulation of cells or cell objects for a certain parameter such as DNA, estrogen, and then measuring the selected cells. The observer in real time views a field of cells and then gates for selection based on the morphological criteria those cells that have the visual parameter such as colored DNA or colored antigen into a subpopulation that is to be measured. The selected cells are examined by digital image processing and are measured for a parameter such as a true actual measurement of DNA in picograms. A quantitation of the measured parameter is generated and provided.

Abstract: An image analysis system is used for the quantitation of nuclear proteins in cell populations. Particularly, the hormonal receptor content of fine needle aspirates of human breast carcinomas are evaluated. Estrogen or progesterone receptors are amplified and visualized in the specimen by a staining technique of the immunoperoxidase type. Monoclonal antibodies specific against the receptor are attached to the receptor sites and are then amplified by a bridging antibody which attaches to the monoclonal antibody and a peroxidase-antiperoxidase complex. A chromagen, diaminobenzidine is combined with the complex and treated with hydrogen peroxide to react with the peroxidase forming an insoluble brown precipitate which marks the receptor sites for optical identification. The specimen is then counterstained with another chromagen, methyl green which is specific to the nucleus of each cell.

Abstract: A method and apparatus is disclosed for use in performing automated classification of cells and other microscopic specimens. The apparatus provides a compact, adjustable assembly that is operable to provide: an operator-apparatus interactive classification system for the cell analysis; alternative techniques for different cells, cytoplasms and cell populations; and enhanced image or color separation and analysis.

Abstract: An image apparatus for measuring true mass characteristics of the specimen in real time is provided with means for controlling the amount and intensity of background light so that the amount of light is held substantially constant and at a level providing reduced background and scattered light so that evaluations at different times on the same or on different image analysis apparatus of the same manufacture result in substantially identical measurements of mass. The light control for the conventional light microscope used with the image analysis apparatus includes four variables which are the light intensity of the light bulb, the size of the field iris, the size of the condenser iris, and the movement the condenser lenses in a vertical or "Z" direction for focus. Preferably, a fixed aperture means in the form of a cup attachment is secured to the condenser iris optics to provide a fixed size iris for the condenser.

Abstract: A user interactive system for dynamically testing and evaluating various cells, antigens, or other materials taken from the human body. More specifically, the DNA in specimen cells is analyzed and quantified by image analysis using pattern recognition techniques. The user is provided with a unique slide or support on which there are specimen and reference materials or objects which are simultaneously stained or otherwise image enhanced at the time of analysis.

Abstract: An apparatus and method are provided for producing signals representative of the mean cell volume of red blood cells in a blood specimen. The apparatus includes means for generating signals repesentative of the area of the cells and means for measuring the optical density of the individual cells and for generating signals representative of the hemoglobin content or mass of the cells. The central pallor is measured for cells having central pallors and means generate a signal representative of the central pallor of these cells. The representative area signals, hemoglobin signals and central pallor signals are sent to a means which generates an output representative of the mean cell volume of the cells.

Abstract: An apparatus for preparing blood samples containing red blood cells for automated analysis wherein the blood sample on a slide is spun to create a monolayer of randomly distributed red blood cells. To inhibit cell morphology distortions from occurring during drying, the morphologies of the cells contained in the monolayer are preserved by a fixing agent after monolayer preparation but prior to drying when such distortions would otherwise develop. The method and apparatus are particularly useful for fixing red blood cells to prevent loss of or deformation of a central pallor which would be detrimental to a subsequent automated analysis.

Abstract: A method for preparing blood samples containing red blood cells for automated analysis wherein the blood sample on a slide is spun to create a monolayer of randomly distributed red blood cells. To inhibit cell morphology distortions from occurring during drying, the morphologies of the cells contained in the monolayer are preserved by a fixing agent after monolayer preparation but prior to drying when such distortions would otherwise develop. The method and apparatus are particularly useful for fixing red blood cells to prevent loss of or deformation of a central pallor which would be detrimental to a subsequent automated analysis.

Abstract: A method and apparatus are disclosed for measuring characteristics of cells, such as red blood cells, and for analyzing parameters of the cell characteristics to define a patient's blood. These parameters may be compared for resemblance to predetermined reference characteristic values for a blood cell pathological condition such as a specific kind of anemia or for a normal blood. A report may be generated showing such resemblance to an anemia or to a normal blood. A report may be generated showing parameters of a multivariate dispersion of distribution for a subpopulation of biconcave cells, an indication of skewness of the distribution of the cells with regard to shape variations in central pallor size; the proportion of abnormal kinds of cells found, and closeness of blood to several specific anemias.

Abstract: A method and apparatus is disclosed for use in performing automated classification of cells of a pap smear as well as other types of cells, such as red blood cells and blood cell neutrophiles. The apparatus generates an image that is split into two paths, (1) a high resolution image of primarily the nucleus of a cell, and (2) a low resolution image of the total cell, nucleus and cytoplasm. An image scanning device located in the first path provides output signals representing the image and circuitry performs measurement and analysis relating to texture of the nucleus. The image in the other path is demagnified which provides an enlarged, lower resolution image of the entire cell, including the nucleus and the cytoplasm and it is projected to a second image scanning device, which provides electrical signals that represent the image of the larger area and circuitry performs measurement and analysis relating to the size, density and color of the cytoplasm and the nucleus.

Abstract: A method and apparatus for automatically classifying abnormal and normal red blood cells is disclosed. The abnormal cells may be differentiated into mutually exclusive subpopulations. The individual hemoglobin characteristic for each red blood cell is measured and a hemoglobin parameter may be reported for each subpopulation of cells. Additionally, cell sizes are measured and the mean cell size and Wintrobe indices may be reported. The interior cell structures for red blood cells are analyzed and the cells are classified based on the presence or lack of a central pallor, their shape, size, and hemoglobin content.

Abstract: In the preparation of blood films for microscopic examination a slide spins in a centrifuge for a time which is a function of the red blood cell concentration of the blood. A drive circuit controls the time of spinning of a slide centrifuge. A variable control for the centrifuge motor includes a manual adjustment which is adjustable across a scale labeled as a function of the percent hematocrit of the blood.