Abstract: A method and apparatus for collecting a cell sample of desired concentration on a filter collection site from a biological liquid specimen in a container. Specimen liquid is moved through a filter while the volume rate of liquid flow through the filter is monitored. The monitored liquid flow rate is compared to a reference value, and liquid flow through the filter is terminated when the ratio of monitored liquid flow rate to the reference value reaches or exceeds a predetermined ratio value. The predetermined ratio value preferably is a function of the protocol for processing the specimen. An alternative method and apparatus relies on the rate of change of the measured weight of the container. This rate is compared to a reference value, and liquid flow through the filter is terminated when the rate of change diminishes to or below a predetermined value.

Abstract: An automated system and method for individually processing multiple specimens of particulate matter-containing liquid in respective containers. The containers are transported seriatim along a processing path to present them to, at least, a preprocessing apparatus (e.g., a mixing head), and then to a specimen acquisition apparatus, which removes preprocessed specimen fluid from the container for subsequent analytical testing or evaluation. Each apparatus is actuated in response to presentation of a container thereto so as to carry out its respective operation independently. An exemplary system can include, in sequential order, stations for container loading and unloading, container uncapping and cap disposal, specimen mixing, filter loading, specimen acquisition (e.g., by aspiration, and then slide printing), filter disposal, and container resealing.

Abstract: A filter assembly for separating and collecting a layer of particulate matter (e.g., cells) from a liquid containing the particulate matter (e.g., a biological fluid specimen). The filter assembly has a holder and contiguous inner and outer fluid pervious media. The outer fluid pervious medium is attached to the sidewall of the holder. The inner fluid pervious medium is of low fluidic impedance relative to the outer fluid pervious medium. The filter assembly is designed for use in a separation housing that defines two flow paths between inlet and outlet, one directly through the filter and the other around the periphery of the filter. The inlet portion of the housing has a central inlet in a radially sloped surface that faces the filter collection site. A movable suction head is adapted to cooperate with the housing and the filter assembly.

Abstract: Apparatus and method for processing specimens, e.g., biological specimens, to extract samples for both liquid (i.e., extracellular) and slide-based (i.e., intracellular) testing. Both types of samples can be obtained from a single fluid specimen. A fluid sampling station removes fluid from a specimen container and places it in a sample receptacle. A specimen acquisition station removes fluid from the container, separates particulate matter (e.g., cells) from the removed fluid, and forms a sample layer of particulate matter, which is transferred to a slide. The two sampling operations can be carried out in any order. The fluid sample receptacle may have a special one-way valve arrangement. The apparatus can be automated so as to process multiple fluid specimens in their respective containers. The machine according to this invention is a “platform instrument” that can produce all required liquid samples and slide-based samples for essentially all cytopathology tests.

Abstract: A vial-based system and method for handling and processing specimens of particulate matter-containing liquid directly in the vial. A processing assembly, which includes a stirrer and a particulate matter separation chamber, is releasably coupled to the inside of the vial cover. The processing assembly remains with the cover when the vial is opened to insert a specimen therein. Application of a particular external force to the closed vial detaches the processing assembly from the cover so that it remains in the vial, for access by automated or manual laboratory equipment, when the cover is subsequently removed.

Abstract: A specimen preview and inspection system is disclosed. The system beneficially includes a preview stage, which provides a set of biasing-information for preview by a technician before the technician formally screens the specimen. The preview stage enables the technician to conveniently review information pertinent to the specimen at issue. The preview stage may thereby bias, or channel, the technician's attention during screening toward diagnostically significant aspects of the specimen. The invention is particularly useful in the context of Pap smear screening, although the invention may extend to inspection of other types of specimens or samples as well.

Abstract: A specimen preview and inspection system is disclosed. The system beneficially includes a preview stage, which provides a set of biasing-information for preview by a technician before the technician formally screens the specimen. The preview stage enables the technician to conveniently review information pertinent to the specimen at issue. The preview stage may thereby bias, or channel, the technician's attention during screening toward diagnostically significant aspects of the specimen. The invention is particularly useful in the context of Pap smear screening, although the invention may extend to inspection of other types of specimens or samples as well.

Abstract: A system for facilitating microscope-based specimen analysis is disclosed. The system includes an improved optical microscope, which may be used, in one application, to analyze cell and tissue samples from specimens obtained from patients, to facilitate inspection of suspicious materials and identification of atypical or abnormal cells and further expert review. The system includes a motorized plate, an automatic focusing sub-system, an improved light source, an improved simple plug connector for direct hookup of the microscope to an external computer, and an electronic image capturing and analyzing sub-system for automatic scanning of the sample and for electronic capture and storage of images indicative of the specimen.

Abstract: A specimen preview and inspection system is disclosed. The system beneficially includes a preview stage, which provides a set of biasing-information for preview by a technician before the technician formally screens the specimen. The preview stage enables the technician to conveniently review information pertinent to the specimen at issue. The preview stage may thereby bias, or channel, the technician's attention during screening toward diagnostically significant aspects of the specimen. The invention is particularly useful in the context of Pap smear screening, although the invention may extend to inspection of other types of specimens or samples as well.

Abstract: A method and apparatus for imaging body tissue utilizing autofluorescence. The apparatus includes an endoscope having a distal end, proximal end and a light processing unit located at the proximal end of the endoscope. The light processing unit accepts light in a spectral region from a light source and directs the light through the endoscope to the tissue located at the distal end of the endoscope. The light excites autofluorescence in the tissue. Optics located in the distal end of the endoscope collect the excited autofluorescence in a spatially resolved manner and routes it to the light processing unit which separates the emitted light from any reflected excitation light. A plurality of imaging detectors receive the emitted light. Each imaging detector is responsive to light in a different spectral band such that an image is generated and interpreted according to a plurality of independent measurements. An apparatus for sampling tissue includes an endoscopic device having a sampling device.

Abstract: A method and apparatus for imaging body tissue utilizing autofluorescence. The apparatus includes an endoscope having a distal end, proximal end and a light processing unit located at the proximal end of the endoscope. The light processing unit accepts light in a spectral region from a light source and directs the light through the endoscope to the tissue located at the distal end of the endoscope. The light excites autofluorescence in the tissue. Optics located in the distal end of the endoscope collect the excited autofluorescence in a spatially resolved manner and routes it to the light processing unit which separates the emitted light from any reflected excitation light. A plurality of imaging detectors receive the emitted light. Each imaging detector is responsive to light in a different spectral band such that an image is generated and interpreted according to a plurality of independent measurements. An apparatus for sampling tissue includes an endoscopic device having a sampling device.

Abstract: A controlled access automated-switching conferencing system includes a special microprocessor-controlled control console disposed at each of a plurality of stations. Each station includes video and audio inputs and outputs. Central automatic video and audio switching devices switch the video and audio inputs so that they may be connected to any one or more of the video and audio outputs, and switch the audio outputs so that they may be connected to one or more audio inputs. A central novel system controller controls the automatic switchers in response to selections of function and station selection members associated with any of the control consoles. An interface is associated with each station for operatively interconnecting the station control console, inputs, and outputs with the system controller, and a central line driver interfaces the system controller with the interface structure.