Optics: measuring and testing – By dispersed light spectroscopy – With sample excitation
Reexamination Certificate
2001-06-15
2003-05-20
Sikder, Mohammad (Department: 2872)
Optics: measuring and testing
By dispersed light spectroscopy
With sample excitation
C356S318000, C356S340000, C356S417000
Reexamination Certificate
active
06567164
ABSTRACT:
CROSS REFERENCE TO RELATED APPLICATIONS
This invention claims priority of the German patent applications 100 30 013.8 and 101 15 486.0 which are incorporated by reference herein.
FIELD OF THE INVENTION
The invention relates to an entangled-photon microscope having a light source and an objective. The invention furthermore relates to an confocal microscope.
BACKGROUND OF THE INVENTION
In scanning microscopy, a sample is illuminated with a light beam in order to observe the reflected or fluorescent light emitted by the sample. The focus of the illumination light beam is moved in an object plane with the aid of a controllable beam deflection device, generally by tilting two mirrors, the deflection axes usually being mutually perpendicular so that one mirror deflects in the x direction and the other deflects in the y direction. The mirrors are tilted, for example, with the aid of galvanometer control elements. The power of the light coming from the object is measured as a function of the position of the scanning beam. The control elements are usually equipped with sensors to ascertain the current mirror setting.
Especially in confocal scanning microscopy, an object is scanned with the focus of a light beam in three space dimensions.
A confocal scanning microscope generally comprises a light source, a focusing lens by which the light from the light source is focused onto a pinhole—the so-called excitation aperture, a beam splitter, a beam deflection device for beam control, a microscope lens, a detection aperture and the detectors for registering the detection or fluorescent light. The illumination light is usually input via a beam splitter. The fluorescent or reflected light coming from the object travels back via the beam deflection device to the beam splitter, and passes through the latter in order to be subsequently focused onto the detection aperture, behind which the detectors are located. Detection light which does not originate directly from the focus region takes a different light path and does not pass through the detection aperture, so that point information is obtained which leads to a three-dimensional image by sequential scanning of the object. A three-dimensional image is usually achieved through layer-by-layer imaging.
In two-photon scanning microscopy, the fluorescence photons that are detected are those attributed to a two-photon excitation process. Such an excitation process can occur whenever two protons of suitable wavelength meet at random in the sample within a narrow time window, namely the lifetime of the virtual intermediate state. The probability of such a quasi-simultaneous meeting is therefore dependent on the square of the photon density, so that high excitation light powers must be achieved in practice. In order to achieve high light powers, it is expedient to pulse the excitation light. This technique is widely known, and is employed both with femtosecond pulses (U.S. Pat. No. 5,034,613; Denk, Strickler, Webb) and with picosecond pulses (DE 44 14 940). Almost all the pulse lasers customarily used at present are mode-locked titanium-sapphire lasers (Ti:sapphire lasers) with pulse repetition rates of 75 MHz-100 MHz. Owing to the high light powers, the sample suffers undesirable bleaching and damage.
It is also customary in multiphoton microscopy, for example in a direct-light arrangement, to detect the fluorescent light on the condenser side without the detection light beam travelling to the detector via the scanning mirrors (non-descan arrangement). In order to achieve three-dimensional resolution, as in the descan arrangement, a detection aperture would be needed on the condenser side. In the case of two-photon or multiphoton excitation, however, the detection aperture can be omitted since the excitation probability in the regions neighbouring the focus is so low that virtually no fluorescent light comes from them. The vast majority of the fluorescent light to be detected therefore originates with high probability from the focus region, which obviates the need for further differentiation, using a detection aperture, between fluorescence photons from the focus region and fluorescence photons from the neighbouring regions.
U.S. Pat. No. 5,796,477 discloses an entangled-photon microscope, which has the advantages of multiphoton excitation but nevertheless avoids extremely high excitation light powers and the consequent disadvantages. Instead of photons which have been formed independently of one another, entangled photons are used to excite the sample.
To produce entangled photons, the said patent proposes a non-linear optical medium, which may be a crystal or a surface, in which two beams of entangled photons are formed by spontaneous parametric downconversion under illumination by a pump light beam. The two beams are guided together when focusing in the sample, and the optical lengths of the beam paths then need to be matched accurately to one another; in practice, this places great demands on the adjustment accuracy and mechanical stability.
During spontaneous parametric downconversion, or parametric fluorescence, two photons are emitted quasi-simultaneously in a two-photon cascade transition. Since these two photons are caused by the same event, i.e. the transition of an electronically excited state to the ground state, and the spin of the overall system (atom and radiation field) is conserved, the polarisation states of the two photons must be coupled together.
The photons find themselves in a so-called quantum-mechanically entangled state. The excitation probability of a fluorophore in the sample, when illuminating with entangled photons, is linearly dependent on the excitation light power rather than on the square of the excitation light power, as in the case of known two-photon excitation; this is because at the focus, entangled photons will in principle always coincide in terms of time and position if the boundary conditions are suitable.
The production of entangled photons using crystals is very inefficient. Furthermore, the known arrangement has the disadvantage that it is compulsory to form two or more beams of entangled photons, which need to be guided separately from one another in the sample such that they overlap at least partially.
SUMMARY OF THE INVENTION
It is an object of the invention to provide an entangled-photon microscope which provides an efficient illumination with entangled photons.
The object is achieved by an entangled-photon microscope comprising:
a light source, an objective, a microstructured optical element arranged between the light source and the objective, wherein entangled photons are produced.
It is a further object of the invention to provide an confocal microscope which provides an efficient illumination with entangled photons.
The object is achieved by a confocal microscope comprising:
a light source, an objective, a microstructured optical element arranged between the light source and the objective, wherein entangled photons are produced.
The invention has the advantage that entangled photons can be produced with higher efficiency than with the known means. The invention also has the advantage that the entangled photons do not need to be guided in spatially separate beams.
In a preferred configuration, the entangled-photon microscope contains a microstructured optical element which is constructed from a plurality of micro-optical structure elements which have at least two different optical densities. The micro-optical structure elements are preferably cannulas, webs, honeycombs, tubes or cavities.
A particularly preferred configuration is one in which the optical element contains a first region and a second region, the first region having a homogeneous structure and a microstructure comprising micro-optical structure elements being formed in the second region. It is also advantageous if the first region encloses the second region.
In another configuration, the microstructured optical element consists of adjacent glass or plastic material and cavities, and is configured as an optical fibre. Elements of this typ
Birk Holger
Engelhardt Johann
Storz Rafael
Foley & Lardner
Leica Microsystems Heidelberg GmbH
Sikder Mohammad
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