Abstract: An optical arrangement for oblique plane microscopy, comprising: an illumination generator arranged to provide abeam of illumination through a first objective lens to illuminate or excite an oblique plane of a sample in use, wherein the first objective lens is also arranged to receive abeam of emitted light from the oblique plane of the sample in use; first and second relay lenses and a second objective lens sequentially arranged to receive the beam of emitted light from the first objective lens and to form, at the focal plane of the second objective lens, an intermediate image having a tilted plane conjugate to that of the oblique plane of the sample; a first mirror located at said focal plane of the second objective lens, arranged to receive and reflect the beam of emitted light; a third relay lens; and an image detector; wherein the second objective lens and the third relay lens are arranged to relay the intermediate image from the first mirror to the image detector; wherein the first minor is also arrange

Abstract: An endoscope includes a light source operable to generate coherent incident light, and a plurality of imaging optical fibers that are arranged in a fiber bundle, arranged to receive light at a proximal end of the fiber bundle, and arranged to transmit light to a distal end of the fiber bundle. The endoscope further includes a spatial light phase modulator between the light source and the fiber bundle, and arranged to receive the incident light from the light source and to adjust the relative phase of the incident light entering each of the plurality of imaging optical fibers.

Abstract: An optical arrangement for oblique plane microscopy includes a first optical subassembly having an objective lens that receives light from a sample in use, and configured to produce an intermediate image of the sample, and a second optical subassembly focused on the intermediate image. Optical axes of the first and second subassemblies are at an angle to each other at the point of the intermediate image, such that the second subassembly images an oblique plane in the intermediate image, corresponding to an oblique plane in the sample. An oblique plane microscopy method is performed by directing an incident light beam through the objective lens to illuminate or excite the oblique plane in the sample, and receiving light from the sample through the same objective lens. The incident light beam is incident on the sample at an angle of substantially 90° relative to the light beam received from the sample.

Abstract: An optical arrangement for oblique plane microscopy includes a first optical subassembly having an objective lens that receives light from a sample in use, and configured to produce an intermediate image of the sample, and a second optical subassembly focused on the intermediate image. Optical axes of the first and second subassemblies are at an angle to each other at the point of the intermediate image, such that the second subassembly images an oblique plane in the intermediate image, corresponding to an oblique plane in the sample. An oblique plane microscopy method is performed by directing an incident light beam through the objective lens to illuminate or excite the oblique plane in the sample, and receiving light from the sample through the same objective lens. The incident light beam is incident on the sample at an angle of substantially 90° relative to the light beam received from the sample.

Abstract: An endoscope includes a light source operable to generate coherent incident light, and a plurality of imaging optical fibres that are arranged in a fibre bundle, arranged to receive light at a proximal end of the fibre bundle, and arranged to transmit light to a distal end of the fibre bundle. The endoscope further includes a spatial light phase modulator between the light source and the fibre bundle, and arranged to receive the incident light from the light source and to adjust the relative phase of the incident light entering each of the plurality of imaging optical fibres.

Abstract: A confocal microscope 2 uses as a light source a two-dimensional array of light emitting diodes 4. A two-dimensional array of detector cells 18 in the form of a CCD camera array or a CMOS camera array is provided. A sequence of illumination patterns are generated by the array of light emitting diodes 4. A corresponding sequence of detection patterns are read from the two-dimensional array of detector cells 18. The light emitting diodes may be A1GaInN light emitting diodes generating light in the wavelength 250 nm to 500 nm. The confocal microscope 2 may be fitted to the tip of an endoscope 30.