GB2343527A - A microscope and a method of manufacturing and operating such a microscope - Google Patents

A microscope and a method of manufacturing and operating such a microscope Download PDF

Info

Publication number
GB2343527A
GB2343527A GB9824483A GB9824483A GB2343527A GB 2343527 A GB2343527 A GB 2343527A GB 9824483 A GB9824483 A GB 9824483A GB 9824483 A GB9824483 A GB 9824483A GB 2343527 A GB2343527 A GB 2343527A
Authority
GB
United Kingdom
Prior art keywords
frequencies
microscope
light
subject
polychromatic light
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB9824483A
Other versions
GB2343527B (en
GB9824483D0 (en
Inventor
Harry Oldfield
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SNOWDEN Ltd
Original Assignee
SNOWDEN Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SNOWDEN Ltd filed Critical SNOWDEN Ltd
Priority to GB9824483A priority Critical patent/GB2343527B/en
Publication of GB9824483D0 publication Critical patent/GB9824483D0/en
Publication of GB2343527A publication Critical patent/GB2343527A/en
Application granted granted Critical
Publication of GB2343527B publication Critical patent/GB2343527B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B27/00Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
    • G02B27/10Beam splitting or combining systems
    • G02B27/12Beam splitting or combining systems operating by refraction only
    • G02B27/126The splitting element being a prism or prismatic array, including systems based on total internal reflection
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/06Means for illuminating specimens
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B27/00Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
    • G02B27/10Beam splitting or combining systems
    • G02B27/1086Beam splitting or combining systems operating by diffraction only
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B27/00Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
    • G02B27/10Beam splitting or combining systems
    • G02B27/14Beam splitting or combining systems operating by reflection only
    • G02B27/145Beam splitting or combining systems operating by reflection only having sequential partially reflecting surfaces

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Microscoopes, Condenser (AREA)
  • Diffracting Gratings Or Hologram Optical Elements (AREA)

Abstract

A microscope includes an illumination source, where the illumination source comprises a source (10) of polychromatic light (15), and means for selecting a combination of frequencies from among the frequencies of the polychromatic light, at selected respective relative intensities to one another, in order to provide non-white polychromatic light for illuminating a subject (25). The frequencies which are selected may be varied, and the relative intensities of the selected frequencies may also be varied. A diffraction grating (50) may be used to select, at least in part, the selected frequencies at the selected relative intensities, and these selected frequencies may then pass through an aperture (23) which may be variable in size to vary the selection of frequencies and/or relative intensities. The selection of frequencies may also be varied by altering the angle of incidence (a) of light upon the diffraction grating (50). A prism (60, fig. 3) may also be used in the place of a diffraction grating (50) in the frequency selection process. The source of polychromatic light may be a source of white light, which may be provided by an incandescent light bulb, or alternatively, the source of polychromatic light may be 3 differently coloured lights (10A-C, fig. 4).

Description

A MICROSCOPE, A METHOD FOR MANUFACTURING A MICROSCOPE AND A METHOD FOR OPERATING A MICROSCOPE The present invention relates to microscopes, and in particular to improvements in optical transmission microscopes.
A typical transmission microscope comprises a light source arranged to supply light to a lower surface of a subject to be viewed. The light may be concentrated by a condenser comprising one or more lenses before reaching the subject. The light reaches the subject, which is mounted on a transparent mount in the path of illumination. Transmission microscopes are usually used for observing subjects which are transparent. The light passes through and around the subject, and is received into an objective, comprising an objective lens and an eyepiece.
When the light passes through and around the subject, the light may be reflected, diffracted, for example at the edges of the subject, absorbed, transmitted with a phase shift, scattered or otherwise modified.
The combination of the modifications imparted to the light by the object produces an image of the subject, which may be observed at the eyepiece.
It is well known to use monochromatic light sources or filters so that monochromatic light illuminates the subject and reaches the eyepiece. Such filters may be used in conjunction with staining of the subject or as an alternative to staining.
Transmission microscopes are often used to observe biological subjects. Biological subjects are often transparent, and difficult to observe. One known apparatus for observing such subjects is the phasecontrast microscope. When light travels through a transparent subject, its phase may be changed. A phase contrast microscope uses an annular diaphragm in the condenser and an annular waveplate in the objective, to provide interference between the diffracted and undiffracted light, observable as an image.
This operation may be used in conjunction with a system of monochromatic filters.
A further optional feature well-known in conjunction with transmission microscopes is dark-field. In this case, the light source is prevented from shining directly into the objective, either by placing an opaque disc in the condenser below the subject, or by illuminating the -subject at an oblique angle. In either case, the subject is lit by peripheral light from the light source, and only light which is diffracted, or reflected by the subject can enter the objective to be observable.
In the various known transmission microscopes, each has a limit to the resolution and the features that are observable in any subject. By using dark field or phase contrast techniques, only a limited amount of light can reach the objective to form an image. This leads to the image being relatively dark, and details are difficult to observe. If monochromatic filters are used, again, much of the available light is excluded from the final image.
To produce improvements in resolution and brightness, very complex expensive microscopes are necessary.
Alternatives to optical microscopes may also be considered, though these types also often result in killing the subject.
For observing biological samples, it has become common practice to stain the samples, and then observe them with a reflected-light microscope, that is, one in which the subject is observed from the same side as that by which it is illuminated. Staining of samples involves use of potentially harmful chemicals which typically also kill the subject to be studied. The staining is required to allow details of the transparent subject to be visible in the reflection microscope.
Sumnarv of the Invention It would be advantageous to provide a microscope of relatively simple construction which enables greater detail of a transparent subject to be observed, without staining. This would allow biological subjects to be observed in their living state, and would avoid the need to handle staining chemicals.
Accordingly, there is provided a microscope comprising an illumination source for illuminating a subject, the illumination source comprising: -a source of polychromatic light; -means for selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another, to provide non-white, polychromatic light for illuminating a subject. According to a further aspect there is provided a method of operating a microscope comprising the steps of: -providing a source of polychromatic light; -selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another to provide non-white, polychromatic light; -illuminating a subject with the non-white, polychromatic light.
According to a further aspect there is provided a method of manufacturing a microscope comprising the steps of: -providing a source of polychromatic light; -providing means for selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another to provide non-white, polychromatic light; -providing means for illuminating a subject with the non-white, polychromatic light.
Preferably the polychromatic light from the source contains a plurality of frequencies, at predetermined fixed respective relative intensities to one another.
Preferably the frequencies of the selected combination of frequencies bear a known or determinable intensity ratio to one another.
Preferably the selected frequencies can be varied.
Preferably the respective relative intensities of the selected frequencies in the light for illuminating a subject can be varied.
Preferably an aperture is provided, through which the selected frequencies pass.
Preferably a variable size aperture which can be adjusted in size is provided to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
Preferably at least one diffraction grating is used for selecting, at least in part, the selected frequencies at the selected relative intensities.
Preferably the at least one diffraction grating is illuminated by the source of polychromatic light.
Preferably at least one diffraction grating is a reflective diffraction grating.
Preferably at least one diffraction grating is a transmission diffraction grating.
Preferably an angle of incidence of illumination of one or more diffraction grating (s) may be varied, so as to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
Preferably an angle of orientation of one or more diffraction grating (s) with respect to the subject may be varied, so as to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
Preferably a prism is used for selecting, at least in part, the selected frequencies at the selected relative intensities.
Preferably the prism is illuminated by the source of polychromatic light.
Preferably the selected combination of frequencies comprises a continuous part of a frequency spectrum.
Preferably the source of polychromatic light is a source of white light.
Preferably the source of polychromatic light comprises an incandescent light bulb.
Preferably a transmission diffraction grating is placed in the path of the non-white polychromatic light, before the subject.
Preferably the transmission diffraction grating is located in a plane substantially perpendicular to the path of the non-white polychromatic light.
Preferably the illumination source further comprises a condenser located for focusing the non-white polychromatic light onto the subject.
In an embodiment of the invention, the selected combination of frequencies may be generated by combining light from a number of sources, each generating light of a restricted range of frequencies. In such an embodiment, relative intensities of the frequencies may be adjusted by adjusting the brightness of each source, such as by using associated dimmers.
Brief Description of the Drawings Preferred embodiments of the present invention will now be described in detail, by way of example only, with reference to the accompanying drawings, in which: Fig. 1 represents a schematic diagram of a microscope, and light passing through it, according to the present invention; Figs 2-4 represent schematic views of alternative light sources, for use with a microscope according to the present invention; and Figs. 5A and 5B show illumination of a subject without, and with, a transmissive diffraction grating located between the light source and the subject; and Fig. 6 shows a ray diagram of different frequencies of light from different positions within the subject being brought to a focus in a single image in a microscope of the present invention.
Detailed Description of the Drawings Fig. 1 shows a microscope modified according to an embodiment of the present invention. As in many conventional microscopes, a light source 10 such as a tungsten incandescent light bulb, or a quartz halogen lamp, or a mercury vapour lamp, provides a beam of polychromatic, preferably white, light 15. The light beam is redirected by a first diffraction grating 50, as will be described later. Part of the redirected light beam passes through an entrance aperture 23 into a condenser 20. The light passes out of the condenser through an exit aperture 24 and via, in a preferred embodiment, a second diffraction grating 75, onto a subject 25 held on a mounting 27, itself supported on a support 30. Part of the light transmitted through the subject and the support enters an objective portion 35 of the microscope comprising an objective lens 37 and an eyepiece 39, to provide an image to an observer 41.
In this particular embodiment, a reflective diffraction grating 50 is provided, located on the optical path of light beam 15 between the light source 10 and the condenser 20.
Light beam 15, comprises a random collection of frequencies of light in the visible range ie white light.
Light beam 15 is incident on diffraction grating 50 and is split into a number of components. A zero order component 52 comprises white light ordinarily reflected from the surface of the diffraction grating. At the outer edges of the zero order, different frequencies are diffracted at different angles to produce coloured edges to the order. The blue end of the spectrum is diffracted least and is seen at the edge of the zero order at the smallest angle with respect to the diffraction grating, whilst the red end of the spectrum is diffracted more and is seen similarly at a greater angle with respect to the diffraction grating, a first order spectrum 54 is produced by diffraction, providing a range of frequencies (colours) varying from R (red) (most diffracted) to B (blue) (least diffracted). Further spectra such as second and third order spectra 56,58, are produced by diffraction, providing a range of frequencies (colours) varying from R' (red) to B' (blue) and from R" (red) to B" (blue) and so on.
High order spectra tend to overlap according to the characteristics of the diffraction grating. The second and third order spectra may overlap to a certain extent, as shown in the figure.
By adjusting the angle of incidence'a'of light 15 on the diffraction grating 50, and/or the angle'b'between the diffraction grating and the centreline P of the microscope, the operator may select part of one, or where different orders overlap, more than one, of the spectra 54-58 produced by the diffraction grating 50. Each spectrum represents a range of light frequencies sorted into frequency order. Selecting light from a part of one spectrum, or more than one if the spectra overlap, for supply into the condenser 20 corresponds to supplying a non-white, polychromatic or coloured light comprising a selected set of frequencies having constant relative intensities to one another for that selected set.
Similarly, adjusting the angle (s)'a'and/or'b' corresponds to selecting a different set of frequencies and/or intensities of frequencies by selecting a different part of the diffracted spectra for supply into the condenser.
To explain further, at greater angles of diffraction as shown in Fig. 1 (the angles of incidence and diffraction are exaggerated in this figure for clarity), overlapping parts of two adjacent spectra (B'-R' (56) and B"- R" (58)) are included in the range of frequencies selected for supply into the condenser. In the example shown in Fig. 1, the condenser 20 receives frequencies corresponding to colours green (G') to orange (O') of the second order spectrum 56, plus colours blue (B") to green (G") of third order spectrum 58. Accordingly, light frequencies corresponding to colours blue to orange are supplied, at relative intensities different to the relative intensities of these colours in incident light beam 15.
The light frequencies and their relative intensities are selected by passage through the entrance aperture 23 and the exit aperture 24 of the condenser. By changing the location, and/or dimensions, of the apertures 23,24, the selection of frequencies and/or relative intensities may be varied. A variable size aperture such as an iris 22 may be provided within the condenser, to allow for general variation in the intensities of the selected light frequencies, and to adjust the selection of the frequencies, to a certain extent.
By tilting the diffraction grating as shown in Fig. 1 clockwise (i. e. by adjusting the angle of incidence'a' of incident light 15, or by adjusting the orientation angle'b'of the diffraction grating with respect to the centreline P and hence subject 25), a different selection of frequencies could be made, for example, colours blue (B') to yellow of the second order spectrum 56, only.
Correspondingly, by tilting the diffraction grating anticlockwise, a different selection of frequencies could be made, for example, colours yellow to red of the second order spectrum 56, plus colours blue (B") to yellow of the third order spectrum 58. Such a selection will contain substantially all visible frequencies of light, but with different relative intensities from the corresponding relative intensities within light beam 15.
As will be appreciated by those skilled in the art, it may be possible to select the same set of frequencies, but simply vary their relative intensities. One way of doing this is to vary angles'a'or'b'and/or the dimensions of the entrance aperture 23 or the exit aperture 24 of the condenser, or by introducing a limitation on the entrance or exit aperture, or a further aperture in the form of, for example, an iris 22. A further option is to change the frequency content and/or relative intensity within light beam 15.
The selected light frequencies which enter the condenser are condensed, or focused, onto the subject 25 under observation. The subject is then observed through the objective 35 in the normal manner.
It has been appreciated by the inventor that many subjects, particularly biological specimens, react differently to different frequencies (colours) of light.
The microscope of the invention takes advantage of this realisation and allows subjects, especially live biological specimens, to be viewed with a clarity, contrast and brightness which, as far as the inventor is aware, has not been possible with similar microscopes before. This has been achieved in a microscope at relatively little cost. Whilst this explanation is not intended to be limiting, the way the invention seems to provide these advantages may be explained as follows.
When white light is used to illuminate a subject, all frequencies of visible light are present, and the resulting image is a combination of the images produced by each frequency. Accordingly, detail of the subject which may be enhanced or picked out by a certain frequency can be obscured by images produced by other frequencies of light so that detail is not picked out. In contrast, if light of a single colour is applied to a subject, features which are enhanced or which react to that particular colour tend to be more easily seen than others, and a meaningful image of the subject may not easily be obtained.
According to the present invention, a variable selected combination of frequencies of light, each frequency having a certain intensity with respect to the other selected frequencies, is applied to the subject.
Accordingly, the features observable with that selected combination of frequencies (colours) at those intensities are visible to the observer. The particular combination of frequencies and relative intensities of frequencies selected can be easily varied to optimise, within the limit of frequencies and intensities available to choose from, the selection for a particular subject 25 under observation. Further, it is thought, without intending to be limiting that the image so produced is less obscured by scattering from within or adjacent to the sample of other colours which do not enhance the image of any particular detail on the subject. Thus, by adjusting the selected combination of frequencies, the details which are picked out in the image may be changed, and the effect of colours which do not enhance any features in the specimen, but rather tend to obscure the overall image, can be limited.
As the reaction of a subject to each frequency of light is individual to that particular subject, it is not possible to generate rules defining an"optimal"setting for the selected frequencies. Thus, it is useful to provide a means for generating a range of frequencies of defined relative intensities, as a function of a variable parameter (here, angles'a'and/or'b'). Thus a set of frequencies and intensities can be selected in a consistent and repeatable manner.
Typically, the microscope should be operated as follows.
Subject 25 on mount 27 is placed on support 30. Light source 10 is illuminated, the diffraction grating adjusted so that some light is directed into the condenser and onto the subject, and the condenser and the objective are adjusted to produce the best available image. Then, the selected frequencies of light are adjusted, in this case by rotating the diffraction grating, until the best possible image is obtained. It may be necessary to adjust the condenser and/or the objective once the selected range of frequencies has been adjusted.
Thus, a combination of frequencies of light is applied to the subject, the combination of frequencies and their relative intensities being adjustable in a repeatable manner so that the image of features of the subject can be optimised within the limit of the system.
The method of the invention allows undesired frequencies of light to be excluded from the image, avoiding the obscuring effect of such frequencies. Accordingly, the apparent resolution of the microscope of the invention seems to be increased over existing microscopes of comparable optics. The images appear more distinct and bright.
According to alternative embodiments of the present invention, various different means for generating nonwhite, polychromatic or coloured light comprising a selected set of frequencies and relative intensities may be provided, as shown in Figs. 2-4. Each alternative is provided with suitable means for adjusting the selected set of frequencies and/or relative intensities in a repeatable manner. For example, calcite crystals typically from Iceland, quartz or other birefringement crystals may be used to select the wavelengths required.
Fig. 2 illustrates the use of a transmission diffraction grating 59. A zero order 52 here corresponds to light directly transmitted through the diffraction grating.
First 54, second 56, and third 58 order spectra are generated by diffraction of the incoming light, and are similar to the spectra discussed with reference to Fig.
1.
Fig. 3 illustrates the use of a prism 60 to generate a spectrum 62 from the light 15. A single spectrum is typically generated, so continuous sectors of the spectrum 62 may be selected for transmission to the subject using this means for generating non-white, polychromatic or coloured light. Further prisms could be added.
In the case of the sources shown in Fig. 2 or Fig. 3, suitable means for adjusting the selected set of frequencies may comprise means for rotating the grating 50 or the prism 60, and/or the position of the light source 10, relative to the centre line of the microscope, to adjust the angles a', a"and/or the angles b', b" illustrated in those figures.
Fig. 4 illustrates a rather different means for generating non-white, polychromatic or coloured light comprising a selected set of frequencies. A number of light sources 10A, 10B, 10C are provided, each including a monochromatic filter 65, 67, 69, for example blue, green and red, respectively. Other monochromatic sources such as lasers may be used, though the cost can be prohibitive. Light 15A, 15B, 15C produced by each coloured source is combined using a series of semisilvered mirrors 70, or other reflective and transmissive means, such as glass sheets. The selected range of frequencies may be selected by choosing which of the lamps 10A-lOC are illuminated at any one time. The relative intensities of the various light frequencies may easily be adjusted by using dimmers to adjust the intensity of each lamp. Such means for generating nonwhite, polychromatic or coloured light may be further refined by adding further lamps of other colours e. g. cyan, magenta and yellow, to provide a greater selection of frequencies from which to choose the set to illuminate the sample. Referring again to Fig. 1, according to a further embodiment of the present invention, a transmission diffraction grating 75 may be placed below the subject 25, between the subject and the condenser. This diffraction grating 75 may be used with any of the means for generating polychromatic light, illustrated in Figs. 1 to 4. It has been found that the presence of this diffraction grating 75 can, for certain subjects, serve to further improve the quality of the image obtained.
Without wishing to be bound by the following description, the inventor believes the improvement seen in the images of subjects especially of living biological matter when a first and/or second (50,75) diffraction grating are introduced into the path of light illuminating the subject to be due to the following effect. In particular, it is believed that the improvement in the brightness of the image is due to the following effect.
Figs. 5A and 5B show a light beam illuminating a subject 25 on a support 27, in the absence of transmission diffraction grating 75, and in the presence of transmission diffraction grating 75, respectively. As shown in FIG. 5A, without the transmission diffraction grating, only light 77 directed at the three-dimensional subject by the condenser reaches the subject, and is available to form an image of the subject. None of light 79 not initially directed towards the subject reaches the subject.
As shown in Fig. 5B, in the presence of the transmission diffraction grating 75 (or indeed grating 50) the light emitted by the condenser is diffracted. Accordingly, some of light 79 which is not initially directed towards the subject and would otherwise miss the subject is diffracted and directed towards the subject 25 and is therefore available to form an image. Much of the light 77 initially directed towards the subject is still received by the subject. Accordingly, the subject 25 seems to receive more light albeit from several different angles of incidence when the transmissive diffraction grating 75 is used. The light is transmitted and scattered by the subject and forms an image.
In addition, use in particular of diffraction grating 75 can improve the image. It seems to homogenise the distribution of the light of different frequencies, and assist in illuminating each part of the subject with each of the selected range of frequencies. However, it is not known for certain that this is how the improvement, seen in the image of certain samples on addition of the second diffraction grating 75 into the path of light just before the sample, works.
A further effect of the microscope of the present invention will now be described. When viewing particularly transparent samples using the microscope of the present invention, the three-dimensional nature of the samples can be observed.
Again, without wishing to be bound by the following description, the inventor believes this improvement to be due to the following effect.
It is well known that many optical systems exhibit chromatic aberration. That is, an optical system will focus light of different frequencies at different points.
Similarly, when polychromatic non-white light is incident on a transparent subject, the light of differing frequencies will come into focus at differing depths in the subject. If the subject is transparent or partially transparent, images formed of these differing depths can be seen in a single final image. To a lesser extent, light of differing frequencies incident on and reflected from the outer surface of a sample, may show the same effect. The focal length of the eye piece may be varied to look at features at differing depths or ranges of depths in the subject.
For example, as shown in Fig. 6, an image 80 of a feature close to the surface of the subject 25 may be focused by the objective at a location 100 in light of a blue frequency. An image of a feature below the surface of the subject may be focused by the objective at the same location 100 in red light. Accordingly, a single image 80 visible to a user in a single plane may contain images corresponding to several layers 25-1,25-2 of the subject 25. If white light is applied to the subject, all images resulting from features at infinitesimally close layers are visible, leading to a generally blurred image. If only monochromatic light is used, only features at the corresponding depth will be visible. However, by using non-white polychromatic or coloured light comprising an optimised selected set of frequencies, only images corresponding to certain selected depths are formed. This seems to lead to a clearer image, and some degree of three-dimensional effect, whereby features appearing at different depths within the subject appear in different colours or different mixtures of colours.
The use of a diffraction grating 50 allows variation in intensity and frequency of the selected group of frequencies, simply and easily, in a consistent and repeatable manner.
The microscope of the invention delivers improved performance when second diffraction grating 75 is used in addition to the first diffraction grating 50, or the alternatives shown in Figures 2-4. However, at least some of the advantages of the present invention may be obtained in a microscope having the second diffraction grating 75 only, or the first diffraction grating 50 (or its alternatives shown in Figures 2-4) only. Alternative sources of light and means for varying the frequencies and/or intensities of a light beam to those described may also be envisaged and fall within the scope of this application.
Example An example of a microscope according to the present invention, suitable for use in viewing biological subjects (such as paramecium, of typical size 100 microns in a sample of pond water is as follows: Reflective diffraction grating 50: 1,000 lines/mm Transmission diffraction grating 75: 600 lines/mm Condenser : Abbe 1.2NA (Numerical Aperture) Objective: Beck lOx 0.25NA Eyepieces: lOx and 20x HUZERNN types Microscope: Beck 47 monocular compound microscope Light source: 40W tungsten incandescent lamp.
In a particular set-up, the angles'a'and'b'may be fixed such that (a+b) =90 . Using the above-described example reflective diffraction grating, an angle of 32 will provide a green/yellow spectrum part towards the condenser 20. A variation of angle'a'of +/-2 will produce a change on the range of frequencies of light entering the condenser.
Although the present invention has been described with reference to certain particular embodiments, the present invention may be applied to other types of microscope.
The inventor has found the present invention to be applicable to many types of transmission optical microscopes. The method of using a microscope according to the present invention may be applied to any type of subject under observation.
The invention may be usefully applied to dark-field or phase contrast microscopes. A dark field microscope may include an opaque disk with an annular aperture, within the condenser. This prevents any light 77 (Figs. 5A, 5B) from entering the objective, the subject being illuminated only by per includes an opaque disk with an annular aperture in each of the condenser and the objective. By applying the modifications according to the present invention, a phase contrast improved image may be produced, corresponding to each of the selected frequencies. Phase contrast techniques have hitherto been applied only to monochromatic imaging.
By rearranging the various components of the microscope, a reflective type of microscope may be provided, in which the subject is illuminated from the same side as it is observed through the objective. The second diffraction grating 75, if used, will be placed in the path of illumination, before the subject. For such improved reflective microscopes, as for the transmission microscopes, at least some of the advantages of the present invention may be obtained in a microscope having the second diffraction grating 75 only, or the first diffraction grating 50 (or its alternatives shown in Figures 2-4) only.

Claims (26)

  1. CLAIMS: 1. A microscope comprising an illumination source for illuminating a subject, the illumination source comprising : -a source of polychromatic light; -means for selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another, to provide non-white, polychromatic light for illuminating a subject.
  2. 2. A method of operating a microscope comprising the steps of: -providing a source of polychromatic light; -selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another to provide non-white, polychromatic light; -illuminating a subject with the non-white, polychromatic light.
  3. 3. A method of manufacturing a microscope comprising the steps of: -providing a source of polychromatic light; -providing means for selecting a combination of frequencies from among the frequencies of the polychromatic light at selected respective relative intensities to one another to provide non-white, polychromatic light; -providing means for illuminating a subject with the non-white, polychromatic light.
  4. 4. A microscope or method according to any preceding claim wherein the polychromatic light from the source contains a plurality of frequencies, at predetermined fixed respective relative intensities to one another.
  5. 5. A microscope or method according any preceding claim in which the frequencies of the selected combination of frequencies bear a known or determinable intensity ratio to one another.
  6. 6. A microscope or method according to any preceding claim in which the selected frequencies can be varied.
  7. 7. A method or microscope according to any preceding claim in which the respective relative intensities of the selected frequencies in the light for illuminating a subject can be varied.
  8. 8. A microscope or method according to any preceding claim in which an aperture is provided, through which the selected frequencies pass.
  9. 9. A microscope or method according to claim 8 in which a variable size aperture which can be adjusted in size is provided to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
  10. 10. A microscope or method according to any preceding claim in which at least one diffraction grating is used for selecting, at least in part, the selected frequencies at the selected relative intensities.
  11. 11. A microscope or method according to claim 10 in which the at least one diffraction grating is illuminated by the source of polychromatic light.
  12. 12. A microscope or method according to claim 10 or claim 11 in which at least one diffraction grating is a reflective diffraction grating.
  13. 13. A microscope or method according to claim 10 or claim 11 or claim 12 in which at least one diffraction grating is a transmission diffraction grating.
  14. 14. A microscope according to any of claims 10-13 in which an angle of incidence of illumination of one or more diffraction grating (s) may be varied, so as to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
  15. 15. A microscope according to any of claims 10-14 in which an angle of orientation of one or more diffraction grating (s) with respect to the subject may be varied, so as to vary the selection of the selected combination of frequencies and/or the selected respective relative intensities.
  16. 16. A microscope or method according to any preceding claim in which a prism is used for selecting, at least in part, the selected frequencies at the selected relative intensities.
  17. 17. A microscope or method according to claim 16 in which the prism is illuminated by the source of polychromatic light.
  18. 18. A microscope or method according to any preceding claim in which the selected combination of frequencies comprises a continuous part of a frequency spectrum.
  19. 19. A microscope or method according to any preceding claim in which the source of polychromatic light is a source of white light.
  20. 20. A microscope or method according to any preceding claim in which the source of polychromatic light comprises an incandescent light bulb.
  21. 21. A microscope according to any preceding claim further comprising a transmission diffraction grating placed in the path of the non-white polychromatic light, before the subject.
  22. 22. A microscope according to claim 21 in which the transmission diffraction grating is located in a plane substantially perpendicular to the path of the non-white polychromatic light.
  23. 23. A microscope according to any preceding claim wherein the illumination source further comprises a condenser located for focusing the non-white polychromatic light onto the subject.
  24. 24. A microscope substantially as described and/or as illustrated in the accompanying drawings.
  25. 25. A method for operating a microscope substantially as described and/or as illustrated in the accompanying drawings.
  26. 26. A method for manufacturing a microscope substantially as described and/or as illustrated in the accompanying drawings.
GB9824483A 1998-11-09 1998-11-09 A microscope,a method for manufacturing a microscope and a method for operating a microscope Expired - Fee Related GB2343527B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB9824483A GB2343527B (en) 1998-11-09 1998-11-09 A microscope,a method for manufacturing a microscope and a method for operating a microscope

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9824483A GB2343527B (en) 1998-11-09 1998-11-09 A microscope,a method for manufacturing a microscope and a method for operating a microscope

Publications (3)

Publication Number Publication Date
GB9824483D0 GB9824483D0 (en) 1999-01-06
GB2343527A true GB2343527A (en) 2000-05-10
GB2343527B GB2343527B (en) 2002-09-18

Family

ID=10842073

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9824483A Expired - Fee Related GB2343527B (en) 1998-11-09 1998-11-09 A microscope,a method for manufacturing a microscope and a method for operating a microscope

Country Status (1)

Country Link
GB (1) GB2343527B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3710091A (en) * 1971-01-27 1973-01-09 J Holcomb Fiber optic illuminator apparatus for scientific instruments
EP0327425A1 (en) * 1988-01-27 1989-08-09 Commissariat A L'energie Atomique Method for optical scanning microscopy in confocal arrangement with large depth of field and apparatus to perform this method
WO1995030919A1 (en) * 1994-05-09 1995-11-16 The Regents Of The University Of California Illuminator elements for conventional light microscopes

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3186296A (en) * 1960-12-09 1965-06-01 Richard T Erban Method and apparatus for microscopic inspection using colored illumination
US3895854A (en) * 1973-10-18 1975-07-22 Coulter Electronics Chromatic method and apparatus for conducting microscopic examinations at a plurality of magnifications
DE8802996U1 (en) * 1988-02-04 1988-06-09 Leica Industrieverwaltung Gmbh, 35578 Wetzlar Adjustable lighting device for uniform illumination of an image field

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3710091A (en) * 1971-01-27 1973-01-09 J Holcomb Fiber optic illuminator apparatus for scientific instruments
EP0327425A1 (en) * 1988-01-27 1989-08-09 Commissariat A L'energie Atomique Method for optical scanning microscopy in confocal arrangement with large depth of field and apparatus to perform this method
WO1995030919A1 (en) * 1994-05-09 1995-11-16 The Regents Of The University Of California Illuminator elements for conventional light microscopes

Also Published As

Publication number Publication date
GB2343527B (en) 2002-09-18
GB9824483D0 (en) 1999-01-06

Similar Documents

Publication Publication Date Title
US4852985A (en) Illuminating device for microscopes
CA2286009C (en) Optical instrument having a variable optical filter
US6563113B1 (en) Microscope, especially a fluorescence microscope, particularly a stereo fluorescence microscope
US6025956A (en) Incident-light fluorescence microscope
JP4108970B2 (en) Total reflection fluorescence microscope with white light source
US6924930B2 (en) Microscope illumination device
JPH11218690A (en) Microscope with vertical fluorescent illuminating optical system
US7480046B2 (en) Scanning microscope with evanescent wave illumination
US20040120034A1 (en) Illumination apparatus for microscope and image processing apparatus using the same
US3895854A (en) Chromatic method and apparatus for conducting microscopic examinations at a plurality of magnifications
WO1999012068A1 (en) Transmission illuminator for microscopes
US20080151226A1 (en) Method for analyzing a sample and microscope for evanescently illuminating the sample
Bancroft et al. Light microscopy
US6850358B2 (en) Scanning microscope and optical element
US20040252379A1 (en) Microscope having at least one beam splitter and a scattered light reducing device
US20030161039A1 (en) Illumination system for microscopy and observation or measuring method using the same
JP2002098899A (en) Fluorescent microscope
EP1218789B1 (en) A microscope, a method for manufacturing a microscope and a method for operating a microscope
GB2343527A (en) A microscope and a method of manufacturing and operating such a microscope
JP4642178B2 (en) Infrared microscope and observation tube used therefor
US10067059B2 (en) Device for simultaneous fluorescence contrasting effect in transmitted light and reflected light
JP5583515B2 (en) Laser microscope illumination device and laser microscope
JP2004012702A (en) Vertical illuminator for fluorescent observation and fluorescent microscope provided therewith
JPH06230200A (en) Sofy x-ray microscope
NL2019089B1 (en) Polarization microscope

Legal Events

Date Code Title Description
732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20111109