Classifications

• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B21/00—Microscopes
  • G02B21/0004—Microscopes specially adapted for specific applications
  • G02B21/002—Scanning microscopes
  • G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
  • G02B21/0032—Optical details of illumination, e.g. light-sources, pinholes, beam splitters, slits, fibers
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B21/00—Microscopes
  • G02B21/0004—Microscopes specially adapted for specific applications
  • G02B21/002—Scanning microscopes
  • G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
  • G02B21/0052—Optical details of the image generation
  • G02B21/0072—Optical details of the image generation details concerning resolution or correction, including general design of CSOM objectives
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B21/00—Microscopes
  • G02B21/06—Means for illuminating specimens

Definitions

• the invention relates to a structured illumination system for three-dimensional microscopy of a sample.
• the illumination of the sample is structured by a movable grid.
• Such structuring allows an improvement in the axial resolution of the system compared to a so-called conventional microscope but it does not improve the lateral resolution.
• the invention more particularly relates to a structured illumination system for three-dimensional microscopy of a sample comprising:
• beam generation means arranged to generate coherent light beams
• an objective having a rear focal plane, the objective being arranged so that the sample is likely to be positioned in the objective focusing plane;
• the illumination system 1 comprises a light source 2, a diffraction grating 3 forming the beam generation means, the diffraction grating 3 being coupled to a filter 7 so as to generate only two coherent diffracted light beams 4a and 4b from the light source 2, a lens 5 arranged to focus the coherent beams 4a and 4b in the rear focal plane PFA of a microscope objective 6, a sample 18 being positioned in the focus plane PMP of the objective 6.
• the coherent beams 4a and 4b are diffracted beams having symmetrical orders p and
• An object of the invention is to improve the axial resolution in such a structured illumination system for three-dimensional microscopy of a sample.
• this document uses a simple grid to generate the diffracted beams, and it does not describe how axial displacement of the sample is performed for axial measurements.
• An object of the invention is to provide a structured illumination system for three-dimensional microscopy of a sample to improve the axial resolution compared to a conventional illumination system.
• the original approach underlying the invention is to simulate the axial displacement of the sample without mechanical displacement.
• Another object of the invention is to provide a structured illumination system for the three-dimensional microscopy of a sample for improving both the axial resolution and the lateral resolution with respect to a conventional illumination system. That is to say to achieve axial resolutions of the order of 0.3 micrometers, and lateral resolutions of the order of 0.1 microns.
• Another object of the invention is to achieve such performance while maintaining an acquisition rate compatible with the study of dynamic phenomena, that is to say greater than or equal to 1 Hertz.
• the beam generating means comprises a spatial light modulator programmed to diffracting a light signal so as to generate at least two coherent diffracted beams not symmetrical with respect to the optical axis of the objective, the spatial light modulator comprising a calculator arranged to apply a constant phase term to each of said at least two coherent beams not symmetrical with respect to the optical axis.
• the sample is illuminated by coherent but non-coherent beams. symmetrical in the axial direction. Therefore, it is possible, by a modification of the distance between the objective and the sample or an axial displacement of the illumination in the sample, to use this non-symmetry, in particular from the difference in illumination between two axial positions of the sample. This thus makes it possible to improve the axial resolution with respect to the Gustaffson et al. mentioned above, and in particular to obtain an axial resolution of less than 0.3 micrometers. According to the invention, this axial displacement is simulated by means of the spatial light modulator by applying a phase term to each of the coherent beams. Thus, the measurement does not require any mechanical displacement and the mechanical losses are therefore reduced.
• the two beams that are not symmetrical with respect to the optical axis of the objective are in particular diffracted diffraction beams of n and p diffraction order with n + p different from 0.
• the lateral resolution maintained around 0.1 micrometers, as in the Gustaffson et al. above.
• a three-dimensional structuring of the illumination has thus been realized, which makes it possible to carry out an axial coding of the illumination in addition to the lateral coding known per se.
• the beam generating means may comprise a light source capable of generating a light signal.
• the beam generating means can be arranged to generate three coherent beams, at least two coherent beams among the three coherent beams being unsymmetrical with respect to the optical axis of the objective.
• the generation of these three coherent beams makes it possible to obtain a structuring of the field symmetrical with respect to the optical axis of the objective and a gain of a factor of two in axial resolution with respect to a lighting with only two coherent beams not symmetrical.
• the beam generation means are arranged so that the three coherent beams generated by diffraction correspond to two diffracted beams of symmetrical diffraction orders and to a zero diffraction order beam.
• the symmetric order beams N and N form, with the zero diffraction order beam, two pairs of beams that are not symmetrical with respect to the optical axis that can be used in the context of the invention.
• the two diffracted beams of diffraction order symmetric diffraction orders can be chosen such that the intensity of the zero diffraction order beam is equal to four times the intensity of one of the order diffracted beams.
• symmetrical diffraction Indeed, it is demonstrated that the improvement of the axial resolution is the best in this case.
• the beams Io and IN are non-symmetrical with respect to the optical axis of the lens. Similarly, the beams I 0 and L N are unsymmetrical with respect to the optical axis of the objective.
• the light signal received from the source 9 it is possible to position a not shown afocal device between the source 9 and the spatial light modulator 10 so as to widen the signal bright, for example five to ten times.
• a sample 14 for example in the form of a fluorescent point object, is positioned in the PMP focusing plane of the objective 12 of the microscope 13 at which the three diffracted beams IN, IN and Io interfere.
• the system 8 described above allows a three-dimensional structuring of the illumination to the sample 14.
• the use of three diffraction orders reveals a Talbot effect in the field transmitted by the objective.
• the spatial light modulator 10 is programmed so as to laterally shift the interference pattern generated by the three diffracted beams in the objective focusing plane.
• This programming makes it possible to simulate a lateral displacement of a diffraction grating generating the three diffracted beams without the modulator physically moving.
• the position of the fluorescent point object is measured in a manner known per se by combining several images or their Fourier transform for different real or simulated positions of the diffraction grating, for example by difference between the intensity the fluorescence received for two real or simulated positions of the diffraction grating.
• the optical distance between the sample 14 and the objective 12 is modified.
• a piezoelectric plate 15 positioned at the level of the sample. 14 or axially moving the objective 12.
• the path of the light beams is illustrated by the illumination system according to the invention.
• the light source 9 generates a light signal in the form of a plane wave 22.
• This plane wave is diffracted by means of beam generation 21 for generating only three diffraction orders lo, IN and IN.
• These beam generation means correspond to the spatial light modulator 10 described with reference to FIG. 2.
• the diffracted beams I 0 , IN and LN are still plane waves.
• the focusing means 19, for example corresponding to a lens or achromatic doublet 19 described above converge these beams towards the back focal plane PFA of the objective 12 of microscope 13. In this way, the beams lo, IN and N L interfere in the PMP focusing plane in the form of plane waves and measurements relating to a sample 14 positioned in the PMP focusing plane can be realized.
• Beam generating means for generating three coherent beams that interfere at the objective focus plane have been described above.
• the effect of improving the axial resolution is then optimal for beams IN, IN and lo, the orders N and -N being chosen as before so that
• the system 8 described above can also easily fit on an existing microscope 13, in parallel with the existing illumination system.
• the microscope 13 may be an existing microscope with an existing objective 12, and the illumination system is adapted so that the beams IN, IN and Io are focused in the PFA rear focal plane of the objective 12.
• a new microscope having a improved resolution allowing full field observation.

Landscapes

• Physics & Mathematics (AREA)
• Chemical & Material Sciences (AREA)
• Analytical Chemistry (AREA)
• General Physics & Mathematics (AREA)
• Optics & Photonics (AREA)
• Microscoopes, Condenser (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=39432831

Family Applications (1)

Country Status (5)

Families Citing this family (7)

Family Cites Families (36)

• 2007
  • 2007-10-18 FR FR0707299A patent/FR2922658B1/fr not_active Expired - Fee Related
• 2008
  • 2008-10-17 US US12/738,573 patent/US8289622B2/en not_active Expired - Fee Related
  • 2008-10-17 WO PCT/FR2008/001469 patent/WO2009090341A2/fr not_active Ceased
  • 2008-10-17 EP EP08870802A patent/EP2201420A2/de not_active Withdrawn
  • 2008-10-17 JP JP2010529427A patent/JP2011501214A/ja active Pending

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events