Abstract: By reducing the outer diameter, increasing the overall length, and correcting chromatic aberration well, the invention realizes an objective optical system and examination apparatus that are suitable for in-vivo examination with a sufficiently increased length and widened observation range. The invention provides a compact objective optical system and an examination apparatus comprising, in order from an object side: a first lens group having positive power; a second lens group including a compound lens; a third lens group formed of a biconvex lens; a fourth lens group having positive power and including a compound lens; and a fifth lens group having positive power. Joining surfaces of the compound lens included in the second lens group and the compound lens included in the fourth lens group have negative power.

Abstract: The invention provides a liquid-immersion objective optical system including a first lens group and a second lens group. The first lens group includes a first lens component having positive refractive power, an object side thereof being a flat surface and a convex surface thereof facing an image-plane side; a second lens component having positive refractive power, a convex surface thereof facing the image-plane side; a third lens component having positive refractive power as a whole, formed by cementing a biconvex positive lens and a negative lens; and a fourth lens component formed by cementing a negative lens and a biconvex positive lens. The second lens group includes a fifth lens component formed by cementing a lens having a concave surface facing the object side and a lens having a convex surface facing the image-plane side; a sixth lens component having positive refractive power; and a seventh lens component having negative refractive power.

Abstract: The invention provides an optical-scanning examination apparatus with a simple configuration, in which the resolution of acquired images can be freely changed and in which the fluorescence image intensity and examination depth can be adjusted to suit the purpose of examination. The optical-scanning examination apparatus includes a light source unit; a focusing lens for forming a first intermediate image of excitation light; an imaging lens; a first objective lens; an optical fiber bundle; a second objective lens; and an imaging unit for imaging return light that returns via the second objective lens, the optical fiber bundle, the first objective lens, and the imaging lens. In addition, a scanning mirror device, which is disposed at the first intermediate image position, is formed of a plurality of mirrors that simultaneously receive the first intermediate image and that can be selectively turned on and off.

Abstract: The invention reduces the loss of fluorescence intensity obtained from a specimen to acquire clear fluorescence images when irradiating the specimen with ultrashort-pulse laser light produced by a laser light source. The invention provides a laser-scanning examination apparatus including a laser light source for producing ultrashort-pulse laser light; a laser light source for producing continuous-wave laser light; a measurement head including an optical scanning unit for scanning the laser light on a specimen and an objective optical system; an imaging unit for detecting return light from the specimen in response to the ultrashort-pulse laser light; and an imaging unit for detecting return light from the specimen in response to the continuous-wave laser light. The laser light sources and one imaging unit are connected to the measurement head by an optical fiber, and the other imaging unit is connected to the measurement head by another optical fiber with a larger core diameter.

Abstract: The invention provides a liquid-immersion objective optical system including a first lens group and a second lens group. The first lens group includes a first lens component having positive refractive power, an object side thereof being a flat surface and a convex surface thereof facing an image-plane side; a second lens component having positive refractive power, a convex surface thereof facing the image-plane side; a third lens component having positive refractive power as a whole, formed by cementing a biconvex positive lens and a negative lens; and a fourth lens component formed by cementing a negative lens and a biconvex positive lens. The second lens group includes a fifth lens component formed by cementing a lens having a concave surface facing the object side and a lens having a convex surface facing the image-plane side; a sixth lens component having positive refractive power; and a seventh lens component having negative refractive power.

Abstract: An examination apparatus that can acquire detailed images from a specimen exhibiting dynamic behavior is provided. The examination apparatus comprises an imaging unit that images a specimen exhibiting dynamic behavior; a behavior detecting unit that detects the dynamic behavior of the specimen; an image storing unit that stores the dynamic behavior of the specimen detected by the behavior detecting unit and images of the specimen imaged by the imaging unit so as to be associated with each other; and a still-image extraction unit that extracts an image of the specimen when the specimen is substantially still based on the dynamic behavior of the specimen from the images of the specimen stored in the image storing unit.

Abstract: The invention provides a multiphoton-excitation-type examination apparatus that efficiently generates a multiphoton-excitation effect, that makes the measurement head compact, and that can be easily adjusted when the measurement head is replaced. The multiphoton-excitation-type examination apparatus comprises a laser light source that oscillates ultrashort pulsed laser light; an optical fiber that transmits the ultrashort pulsed laser light from the laser light source; a support member; a measurement head supported on the support member so as to be movable upwards and downwards and at an angle, and having an optical system that irradiates a specimen with the ultrashort pulsed laser light transmitted by the optical fiber that measures fluorescence or reflected light coming from the specimen; and a dispersion-compensating member, in the measurement head, that compensates for group velocity dispersion of the ultrashort pulsed laser light irradiated onto the specimen.

Abstract: A compact laser-scanning microscope that allows in-vivo observation, particularly of cells, with wavelengths ranging from the visible to the infra-red, can be provided. The laser-scanning microscope includes a laser light source unit, an optical fiber, a collimator optical system, an optical scanning unit, a pupil projection optical system, an objective optical system, and a detection optical system that detects fluorescence or reflected light from the specimen, via the objective optical system, the pupil projection optical system, the optical scanning unit, the collimator optical system and the optical fiber. The objective optical system can be attached to and detached from the pupil projection optical system near the intermediate image position.

Abstract: The invention provides an optical-scanning examination apparatus with a simple configuration, in which the resolution of acquired images can be freely changed and in which the fluorescence image intensity and examination depth can be adjusted to suit the purpose of examination. The optical-scanning examination apparatus includes a light source unit; a focusing lens for forming a first intermediate image of excitation light; an imaging lens; a first objective lens; an optical fiber bundle; a second objective lens; and an imaging unit for imaging return light that returns via the second objective lens, the optical fiber bundle, the first objective lens, and the imaging lens. In addition, a scanning mirror device, which is disposed at the first intermediate image position, is formed of a plurality of mirrors that simultaneously receive the first intermediate image and that can be selectively turned on and off.

Abstract: A microscope system includes a light source and an objective unit. The objective unit includes an objective optical system, including a small-diameter distal optical system arranged at an end brought near to or into contact with a specimen, for focusing light from the light source onto the specimen; a threaded mount at a coupling position; and an outer cylinder enclosing the small-diameter distal optical system. The microscope system further includes an imaging optical system for forming an image of light from the specimen through the objective optical system and a microscope main body for housing the imaging optical system. The objective unit is detachable from and attachable to the microscope main body with the threaded mount. Conditional expression Df/Da?0.3 is satisfied, where Df represents the outer diameter of the outer cylinder and Da represents the outer diameter of the threaded mount.

Abstract: An optical imaging apparatus has an optical scanning probe configured to irradiate low-coherence light onto a subject and to perform photo-reception of light scattered at the subject, and an observation device adapted to construct a cross-section image of the subject based on information from the light received through the optical scanning probe. The optical scanning probe is detachably connected to the observation device.

Abstract: The invention aims to make it unnecessary to reposition an objective lens when repeatedly carrying out examinations. It is possible to carry out in vivo examination of tissue such as cells and muscle tissue or various internal organs, such as the heart, liver, and so forth, of mammals, especially small experimental animals, over a comparatively long period of time. A microscope system having an objective optical system unit and a structure or member for fixing the objective optical system unit to a living body is provided.

Abstract: A control portion of an optical image pickup apparatus includes a scan driver, a lock-in amplifier, and an A/D converter. The scan driver outputs a predetermined drive signal to a Y-scanning mirror and an X-scanning mirror and scans the Y-scanning mirror and the X-scanning mirror. The lock-in amplifier detects a signal level Vout of a frequency component of the drive signal of the scan driver among signals detected by a detector portion. The A/D converter converts a signal detected by a detector portion 5 and a signal level of the detected signal of a frequency component of a drive signal detected by the lock-in amplifier to digital signals and outputs the digital signals to an image processor 7. Thus, mirror scan operations of the scanning mirrors can be securely detected.

Abstract: Before performing observation with an optical scanning probe using a low-coherence light source and the like, a shutter is inserted in a reference light side optical path to create a state wherein interference light does not occur, in which state a reference member is set to a focal position of a converging optical system such that the output of a light detector is maximal by moving the reference member by a driving device at an observation light optical path side of an optical scanning probe, following which the shutter is opened, and the position of a mirror at the reference light side is moved and set such that the output of the light detecting means is maximal, thereby enabling the optical scanning observation apparatus to be set to a state of suitable optical properties, easily and smoothly.

Abstract: An imaging system for use with an endoscope, including a light source which emits white light and excitation light which will produce a fluorescence response by an object under inspection, an imaging camera including separate paths for processing images produced by white light and excitation light, a selection device that causes the imaging device to operate in a white light mode or an excitation light mode, and a protective device that prevents damage to high-sensitivity imaging components from exposure to excessive light input. Fluorescent image data are separated into at least red and green color bands which are separately processed to produced a video display in which normal tissue is displayed in predetermined specific color, and abnormal tissue in one or more distinctly different colors. In one embodiment, an image color interpretation guide is provided in the form of multiple color bars which are superimposed on a single video display device with the image display. of different kinds.

Abstract: An optical imaging device includes a reference scanning unit offering a high signal-to-noise ratio and capable of scanning an object rapidly. An interference optical system can be realized inexpensively. In the optical imaging device, low coherent light passed through an optical coupler and another optical coupler, irradiated from an optical scanner probe, reflected from an observed point in a living tissue, returned to the optical coupler, propagated over a fourth SM optical fiber, and routed to another optical coupler shall be referred to as sample light. Light passed through an optical length variation optical system via the optical coupler and routed to the optical coupler shall be referred to as reference light. At this time, a difference between a delay time undergone by the sample light and a delay time undergone by the reference light is proportional to a difference between an optical length for the sample light and an optical length for the reference light.

Abstract: An endoscope includes an optical system for endoscope observation arranged in an edge of an inserting portion which can be inserted in a specimen, an optical system for microscopic observation which microscopically observes an observing portion of the specimen, a moving mechanism for adjusting an angle of view which changes the angle of view by moving a part of the optical system for endoscope observation, and a focal-point adjusting mechanism which is arranged in the edge of the inserting portion and which moves a focal point on the side of a subject in the optical system for microscopic observation, wherein the moving mechanism for adjusting the angle of view and the focal-point adjusting mechanism are arranged forward and backward of the same axis to the inserting portion.

Abstract: It is an object of the present invention to provide a process for a fluorine containing carbon film (a CF film), which can put an interlayer insulator film of a fluorine containing carbon film into practice. A conductive film, e.g., a TiN film 41, is formed on a CF film 4. After a pattern of a resist film 42 is formed thereon, the TiN film 41 is etched with, e.g., BCl3 gas. Thereafter, when the surface of the wafer is irradiated with O2 plasma, the CF film is chemically etched, and the resist film 42 is also etched. However, since the TiN film 41 functions as a mask, a predetermined hole can be formed. Although an interconnection layer of aluminum or the like is formed on the surface of the CF film 4, the TiN film 41 functions as an adhesion layer for adhering the interconnection layer to the CF film 4 and serves as a part of the interconnection layer. As the mask, an insulator film of SiO2 or the like may be substituted for the film.

Abstract: An optical imaging device includes a reference scanning unit offering a high signal-to-noise ratio and capable of scanning an object rapidly. An interference optical system can be realized inexpensively. In the optical imaging device, low coherent light passed through an optical coupler and another optical coupler, irradiated from an optical scanner probe, reflected from an observed point in a living tissue, returned to the optical coupler, propagated over a fourth SM optical fiber, and routed to another optical coupler shall be referred to as sample light. Light passed through an optical length variation optical system via the optical coupler and routed to the optical coupler shall be referred to as reference light. At this time, a difference between a delay time undergone by the sample light and a delay time undergone by the reference light is proportional to a difference between an optical length for the sample light and an optical length for the reference light.

Abstract: A compact optical unit which comprises a light emitting section for emitting a light, a first optical element having a first reflecting section for reflecting a light which is emitted from the light emitting section, a second optical element having a second reflecting section which is disposed to face the first optical element, and a light condensing optical system for condensing a light is formed. The first reflecting section and the second reflecting section are disposed so as to be diagonal to an optical axis of a light which is incident to the first reflecting section and the second reflecting section, a light transmitting section is disposed in the first optical element for transmitting a light which is reflected by the second reflecting section so as to be incident to the light condensing optical system.