Abstract:
The present invention features two flat-field, telecentric, infinite conjugate, achromatic objectives (32 and 34) each of which has an external pupil lying in a common plane located equidistant from the two objectives, defining a mechanically accessible central pupil (30) of an imaging system centered in the common plane (28). Each of the objectives is afocal in the common plane, with one of the lenses forming a focal plane proximate to a sample. The lenses are adapted to provide varying levels of magnification while keeping constant the number of resolvable points in the field of view. An array detector (14) is positioned proximate to a focal plane formed of the remaining objective lens (34). The double objective lens assembly is described as being included in transillumination and epi-illumination systems.
Abstract:
A compact, movable scan head (10) has multiple scanning modalities, capable of high speed and high resolution scanning of a variety of samples (20). Stimulation and detection of storage phosphor screens and fluorescent samples (20) are preferably achieved with first and second channels (81, 82) in an optical path of a first side (11) of the scan head (10). The first side (11) preferably has a laser diode light source (14). Reading of reflective and transmissive signals is also possible. A third channel (83) is available in the optical path of a second side (12) of the scan head (10). The third channel preferably provides LED (32) point scanning and reading of fluorescent, reflective and transmissive signals received from the sample (20). The various modalities of the scan head (10) have coincident optical paths.
Abstract:
A sample substrate (51, Fig. 4A) for use in a fluorescence imaging system (Fig. 1) includes a rigid base with a specularly reflective surface, typically metal, on which is deposited a transparent coating layer (53). The coating layer has a thickness selected so that a particular fluorescence excitation wavelength, corresponding to a specified fluorescent constituent to be sought in sample material, has an optical path from the top of the coating layer to the reflecting surface in the base of substantially an odd multiple of one-quarter wavelength, so that the standing wave of the fluorescence excitation wavelength of light incident of the substrate has an antinode (61) located at or near where sample material would be disposed on top of the coating layer. This maximizes fluorescence excitation of the sample on the reflective substrate. The transparent coating layer may be a dielectric material (e.g. silica) or may be a multilayer structure with a top layer of biologically active material for binding a specified sample constituent.
Abstract:
Provided is a coaxial illumination and collection laser scanning system designed to provide substantially uniform detection sensitivity across the field of view of an objective lens (27; 127) by reducing lateral chromatic aberrations at the expense of amplifying axial chromatic aberrations. Axial chromatic aberrations in the system are removed in the path of a retro-beam (31). A laser (18; 117, 118) is in optical communication with the objective lens. The laser (18; 117, 118) produces a collimated beam of coherent light (19; 119) that is directed by a scanner (25) through the objective lens (27; 127) to illuminate a raster of spots on the sample's surface (29), thereby stimulating a series of small regions of the sample to emit light.
Abstract:
Fluorescence imaging system includes objective (21) which is achromatic and has an external entrance pupil (29), serves as a condenser for the system, and positioned above sample (23) in close proximity to one another. Laser (18) directs collimated light (19) to scan device (20) located at entrance pupil (29). Scan device (20) reflects, refracts, or diffracts light through objective (21) to illuminate a spot (22) on the sample's surface, and illuminates a line or an area on the sample surface by varying the angle of laser light into objective (21). Sample (23) emits fluorescent light (24) in response to the illumination. The fluorescent light (24) is collected by objective (21) and passes through the system along the path of the illumination light. Wavelength-discriminating dichroic filter (25), placed along the optical axis between laser (18) and objective (21), directs fluorescent light (24) onto photodetector (26) to produce a signal representing the sample surface emitting the fluorescent light. Display (37) displays the digitized data in a raster format.
Abstract:
An LED point imaging scanner for stimulating and reading fluorescent and reflective signal radiation from a target sample (10) is disclosed. LED light source (12) is mounted on scan head (20) and focused into pinhole aperture (15) of spatial filter (30), then collimated and focused to a spot (17) on sample (10). The spatial filter, or an optical fiber equivalent, effectively restricts the incoherent LED light and creates a point light source. Signal radiation from sample (10) is collected through scan head (20) and the returning light beam is collimated and focused onto detection means (40). A spatial filter (22) in the path of the returning beam may also be utilized. Detection means (40) is either a small detector directly mounted onto the scan head, or an end of an optical fiber which transmits the point image to a remotely-positioned stationary detector. The scan head is moved along one or two axes relative to the sample.
Abstract:
A fluorescence imaging system that includes an objective that is both achromatic and has an external entrance pupil. The objective also serves as a condenser for the system which substantially reduces the system's cost and footprint. With the objective positioned above a sample so that they are in close proximity to one another, a laser directs a collimated beam of light to a scan device located at the objective entrance pupil. The scan device reflects, refracts, or diffracts the light through the lens to illuminate a spot on the sample's surface. The scan device illuminates a line or an area on the sample surface by varying the angle of laser light, in one or two dimensions, into the objective. The sample emits fluorescent light in response to the illumination. The fluorescence light is collected by the objective and passes through the system along the path of the illumination light. A wavelength-discriminating dichroic filter is placed along the optical axis between the laser and the objective to direct the fluorescent light onto a photo-detector to produce a signal representing the sample surface emitting the fluorescent light. A display device is provided that displays the digitized data in a raster format.