摘要:
A system and a method for imaging microfluidic ejectors during operation. An example provides a microscopy system, that includes a plurality of microfluidic ejectors. A mirror is disposed in a droplet path of the plurality of microfluidic ejectors, wherein the droplet path passes through an opening in the mirror. An optical system is focused on the plurality of microfluidic ejectors through the mirror, wherein the optical system comprises a camera.
摘要:
A 2D spatial differentiator operates in transmission and comprises a Si nanorod photonic crystal that can transform an image, Ein, into its second-order derivative, Eout α ∇2 Ein, allowing for direct discrimination of the edges in the image. The use of a 2D photonic crystal allows for differentiation and edge detection in all directions with a numerical aperture (NA) up to 0.315 and an experimental resolution smaller than 4 μm. The nanophotonic differentiator is able to be directly integrated into an optical microscope and onto a camera sensor, demonstrating the ease with which it can be vertically integrated into existing imaging systems. Furthermore, integration with a metalens is demonstrated for realizing a compact and monolithic image-processing system. In all cases, the use of the nanophotonic differentiator allows for a significant reduction in size compared to traditional systems, opening new doors for optical analog image processing in applications involving computer vision.
摘要:
A system for characterizing at least one particle from a fluid sample is disclosed. The system includes a filter disposed upstream of an outlet, and a luminaire configured to illuminate the at least one particle at an oblique angle. An imaging device is configured to capture and process images of the illuminated at least one particle as it rests on the filter for characterizing the at least one particle. A system for characterizing at least one particle using bright field illumination is also disclosed. A method for characterizing particulates in a fluid sample using at least one of oblique angle and bright field illumination is also disclosed.
摘要:
An illumination arrangement includes illumination optics defining an optical axis and a light source for generating at least one illumination beam path for illuminating an object field at a specific illumination angle with a viewing beam path. At least one mirror is provided in the illumination beam path for deflecting light from the light source and the mirror has a longitudinal extent along the optical axis. A light-emitting surface region of the light source is variable (x) perpendicular to the optical axis without movable components. The illumination optics are embodied in such a way for obtaining a desired illumination that an illumination pupil is imaged within the longitudinal extent of the mirror.
摘要:
A light field representation of a sample is synthesized or simulated based on bright field image data and phase image data acquired by a microscope such as a quantitative phase microscope. The light field representation may be utilized to render three-dimensional representations of the sample.
摘要:
An illumination arrangement includes illumination optics defining an optical axis and a light source for generating at least one illumination beam path for illuminating an object field at a specific illumination angle with a viewing beam path. At least one mirror is provided in the illumination beam path for deflecting light from the light source and the mirror has a longitudinal extent along the optical axis. A light-emitting surface region of the light source is variable (x) perpendicular to the optical axis without movable components. The illumination optics are embodied in such a way for obtaining a desired illumination that an illumination pupil is imaged within the longitudinal extent of the mirror.
摘要:
A side camera is combined with a conventional optical metrology system to image the object during the focusing scan performed in normal focusing procedures. The camera is positioned in fixed spatial relation to the objective and with its focal plane in substantial alignment with the optical axis of the objective so as to image the object during the scan. The camera is used to monitor the illumination spot formed on the object by the beam projected through the system's objective. The in-focus position is found by moving the object such that the illumination spot coincides with the objective's focus seen through the camera.
摘要:
An instrument and method for scanning large microscope specimen on a specimen holder has a scanning optical microscope that is configured to scan the specimen in one of brightfield and fluorescence. The specimen is dynamically tillable about a scan direction during a scan to maintain focus along the length of each scan line as the scan proceeds. A three dimensional image of the specimen can be obtained wherein the specimen tilt and relative focus are maintained from a first image contour to a second image contour through a thickness of a specimen.
摘要:
An instrument for scanning a specimen has a two-dimensional sensor array, the sensor array containing a mosaic colour filter array or a scanning colour filter array. The instrument can be operated in fluorescence or in brightfield. The scanning colour filter array has the same colour throughout each row with adjacent rows having different colours.
摘要:
An illumination system for a microscope, including a light source for generating light to illuminate a sample for microscopic observation, at least one collimating lens for collimating light generated by the light source, and a darkfield condenser for receiving collimated light and directing a hollow cone of light onto the sample under observation. The system optionally includes an adapter for enhancing economy of light transmission from the light source to the specimen, the adapter having a centrally disposed spacer and a plurality of optical fibers surrounding the spacer, to generate a hollow cylinder of light for transmission to the darkfield condenser. The system provides improved resolution and contrast, and is well suited for adaptation to fluorescence microscopy techniques.