Controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof

Information

  • Patent Grant
  • 9099214
  • Patent Number
    9,099,214
  • Date Filed
    Tuesday, December 11, 2012
    12 years ago
  • Date Issued
    Tuesday, August 4, 2015
    9 years ago
Abstract
A method includes providing a capability to control divergence of a coherent light beam having an axially symmetrical distribution of intensity thereof through an optical divergence controller, and directing an output of the optical divergence controller related to the controlled divergence of the coherent light beam onto a glass prism. The glass prism includes a planar shape onto which a pyramidal structure is formed. The method also includes controlling a distance between maxima of an output light field of the glass prism and intensity thereof through controlling the divergence of the coherent light beam through the optical divergence controller and/or varying a distance between the optical divergence controller and the glass prism, and utilizing the output light field of the glass prism in controlling microparticles in a microtechnology or a nanotechnology application.
Description
CLAIM OF PRIORITY

This patent application claims priority from Application Serial No. u20110312, titled DEVICE FOR FORMATION OF LIGHT FIELD WITH CELLULAR INTENSITY DISTRIBUTION IN TRANSVERSAL SECTION filed on Apr. 19, 2011.


FIELD OF TECHNOLOGY

This disclosure relates generally to controlling microparticles and, more particularly, to controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof.


BACKGROUND

Gradient light beams may be utilized for capturing and/or shifting of microparticles (e.g., influencing ensembles of micro-objects in microtechnology and/or nanotechnology applications with aims including but not limited to regulating movement and/or mixing thereof with regard to organic tissues as part of therapy and/or prophylaxis and influencing materials during localized laser processing). The mechanism of particle capturing may be based on aligning particle dipoles along the direction of a light field. When the light field contains a strong gradient, the particles may be attracted to a region of strongest electric field. The gradient may influence particles in a plane perpendicular to the axis of the light field.


When the longitudinal gradient force balances a dispersion force, the particles having higher refractive index than that of the environment may be captured and localized in intensity maxima of the light field. The particles having lower refractive index than that of the environment may be retracted in local intensity minima of the light field. Optical tweezers utilized for manipulating viruses and bacteria, inducing cellular synthesis in immunology and molecular genetics, capturing and shifting chromosomes, changing mobility of human spermatozoa and trans-membrane proteins etc. may be created based on the aforementioned principle. Gradient light fields may also be utilized for creating optical pumps, funnels and the like with an aim of filtrating particles and/or influencing living and non-living matter.


Devices utilized for forming gradient light fields may not allow for locally rounded intensity maxima to be formed. Although a Fresnel biprism allows formation of a static gradient light field in the form of parallel strips, the Fresnel biprism may not allow formation of a variable gradient light field in addition to not enabling formation of a light field having locally rounded intensity maxima.


An optical setup including a source of laser radiation, a telescope-collimator and a pyramid with four edges may enable formation of a gradient light field (e.g., a quadrabeam). However, the aforementioned gradient light field may be static, with a multitude of periodically distributed intensity maxima having same magnitudes in a transverse direction.


SUMMARY

Disclosed are a method, a device and/or a system of controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof.


In one aspect, a method includes providing a capability to control divergence of a coherent light beam having an axially symmetrical distribution of intensity thereof through an optical divergence controller, and directing an output of the optical divergence controller related to the controlled divergence of the coherent light beam onto a glass prism. The glass prism includes a planar shape onto which a pyramidal structure is formed. The glass prism is positioned such that the output of the optical divergence controller is incident on a planar surface of the planar shape or the pyramidal structure.


The method also includes controlling a distance between maxima of an output light field of the glass prism and intensity thereof through controlling the divergence of the coherent light beam through the optical divergence controller and/or varying a distance between the optical divergence controller and the glass prism, and utilizing the output light field of the glass prism in controlling microparticles in a microtechnology or a nanotechnology application.


In another aspect, an optical device includes an optical divergence controller to provide a capability to control divergence of a coherent light beam having an axially symmetrical distribution of intensity thereof, and a glass prism including a planar shape onto which a pyramidal structure is formed. The glass prism is positioned such that an output of the optical divergence controller is incident on a planar surface of the planar shape or the pyramidal structure. Controlling the divergence of the coherent light beam through the optical divergence controller and/or varying a distance between the optical divergence controller and the glass prism enables controlling a distance between maxima of an output light field of the glass prism and intensity thereof. The output light field of the glass prism is configured to be utilized in controlling microparticles in a microtechnology or a nanotechnology application.


In yet another aspect, an optical system includes an optical divergence controller to provide a capability to control divergence of a coherent light beam having an axially symmetrical distribution of intensity thereof, and a glass prism including a planar shape onto which a pyramidal structure is formed. The glass prism is positioned such that an output of the optical divergence controller is incident on a planar surface of the planar shape or the pyramidal structure. The optical system also includes an ensemble of microparticles.


Controlling the divergence of the coherent light beam through the optical divergence controller and/or varying a distance between the optical divergence controller and the glass prism enables controlling a distance between maxima of an output light field of the glass prism and intensity thereof. The output light field of the glass prism is configured to be utilized in controlling the ensemble of microparticles.


The methods and systems disclosed herein may be implemented in any means for achieving various aspects, and may be executed in a form of a machine-readable medium embodying a set of instructions that, when executed by a machine, cause the machine to perform any of the operations disclosed herein. Other features will be apparent from the accompanying drawings and from the detailed description that follows.





BRIEF DESCRIPTION OF THE DRAWINGS

The embodiments of this invention are illustrated by way of example and not limitation in the figures of the accompanying drawings, in which like references indicate similar elements and in which:



FIG. 1 is a schematic view of an optical system, according to one or more embodiments.



FIG. 2 is a ray diagram of a convergent beam incident on a glass prism of the optical system of FIG. 1, according to one or more embodiments.



FIG. 3 is a ray diagram of a divergent beam incident on the glass prism of the optical system of FIG. 1, according to one or more embodiments.



FIG. 4 is a perspective view of the glass prism of the optical system of FIG. 1.



FIG. 5 is a plot of a longitudinal distribution of a convergent cellular field as a function of distance between the glass prism and an optical divergence controller of the optical system of FIG. 1.



FIG. 6 is a plot of a longitudinal distribution of a divergent cellular field as a function of distance between the glass prism and an optical divergence controller of the optical system of FIG. 1.



FIG. 7 is a process flow diagram detailing the operations involved in controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof, according to one or more embodiments.





Other features of the present embodiments will be apparent from the accompanying drawings and from the detailed description that follows.


DETAILED DESCRIPTION

Example embodiments, as described below, may be used to provide a method, a device and/or a system of controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof. Although the present embodiments have been described with reference to specific example embodiments, it will be evident that various modifications and changes may be made to these embodiments without departing from the broader spirit and scope of the various embodiments.



FIG. 1 shows an optical system 100, according to one or more embodiments. In one or more embodiments, optical system 100 may include a laser source 102 and a telescope collimator 104 configured to form a collimated coherent beam of light with axially symmetrical distribution of intensity. In one or more embodiments, the collimated coherent beam of light may be directed onto an optical divergence controller 106 that is configured to control divergence of the collimated coherent beam of light. In one example embodiment, optical divergence controller 106 may be a spherical lens with varying focal distance. Depending on the adjustment of optical divergence controller 106, convergent or divergent light beams may be generated therefrom.


In one or more embodiments, optical system 100 may include a glass prism 108 onto which the convergent or the divergent beam from optical divergence controller 106 is incident. In one example embodiment, glass prism 108 may include a rectangular cuboid onto which a square pyramid is formed. In one or more embodiments, a pyramidal surface of glass prism 108 may be a pure pyramid; alternately, the pyramidal surface may be a pyramid truncated on an edge thereof in a different manner (e.g., truncated on a square-shaped plane, a round-shaped plane, arbitrarily truncated). The shape(s) of glass prism 108 shown in FIG. 1, therefore, should not be considered limiting. In one example embodiment, glass prism 108 may be positioned such that the light beam is incident on a planar surface of the rectangular cuboid, with the square pyramid (an example shape) being along the direction of incidence; it should be noted that glass prism 108 may also be positioned such that the light beam is incident on a prism side thereof (and similarly for other variations of glass prism 108).


In one or more embodiments, when a convergent light beam is incident on glass prism 108, a convergent quadrabeam may be formed, with the convergent quadrabeam representing a cellular field in which the distance between maxima (or, cell period) decreases proportionally with distance. In one or more embodiments, when a divergent light beam is incident on glass prism 108, a divergent quadrabeam may be formed, with the divergent quadrabeam representing a cellular field in which the distance between maxima (or, cell period) increases with distance.


In one or more embodiments, through increasing divergence of the beam incident on glass prism 108 through optical divergence controller 106, the intensity of maxima of the cellular field and distances between maxima thereof (or, cell period) may be increased. Likewise, through decreasing divergence of the beam incident on glass prism 108 through optical divergence controller 106, the intensity of maxima of the cellular field and the distances between maxima thereof (or, cell period) may be decreased.


In one or more embodiments, with an increase in a width (or, dimension along the direction of incidence of the beam) of the square pyramid portion of glass prism 108, the distance between maxima of the cellular field (or, cell period) may increase. Likewise, with decrease in the width of the square pyramid portion of glass prism 108, the distance between maxima of the cellular field (or, cell period) may decrease. Thus, it may be possible to tune the distance between the maxima of the cellular field (or, cell period) through tuning divergence and/or through utilizing glass prisms (e.g., glass prism 108, or, another glass prism instead of glass prism 108) of varying widths.



FIG. 1 also shows a microscope 110 and a Charge Coupled Device (CCD) camera 112 to observe, register and/or investigate the cellular field. It is obvious that the aforementioned devices have been included merely for illustrative purposes, and that other devices within an experimental setup are within the scope of the exemplary embodiments. FIG. 2 shows a ray diagram of a convergent beam incident on glass prism 108, according to one or more embodiments. FIG. 3 shows a ray diagram of a divergent beam incident on glass prism 108, according to one or more embodiments. FIG. 4 shows a perspective view of glass prism 108, according to one or more embodiments.



FIG. 5 shows the longitudinal distribution of a convergent cellular field as a function of distance between glass prism 108 and optical divergence controller 106. As seen in FIG. 5, when the distance between glass prism 108 and optical divergence controller 106 is increased (from 10 mm to 50 mm to 90 mm), the distance between maxima in the intensity distribution across a transverse section of the convergent cellular field decreases. The beam incident on glass prism 108 may be more convergent as the distance between glass prism 108 and optical divergent controller 106 is increased, thereby contributing to the distance between maxima in the cellular field being reduced.



FIG. 6 shows the longitudinal distribution of a divergent cellular field as a function of distance between glass prism 108 and optical divergence controller 106. As seen in FIG. 6, when the distance between glass prism 108 and optical divergence controller 106 is increased (from 10 mm to 50 mm to 90 mm), the distance between maxima in the intensity distribution across a transverse section of the divergent cellular field increases. The beam incident on glass prism 108 may be more divergent as the distance between glass prism 108 and optical divergent controller 106 is increased, thereby contributing to the distance between maxima in the cellular field being increased.


Thus, in one or more embodiments, optical system 100 may allow for formation of a gradient light field with a cellular distribution of intensity in a transverse section thereof, the cellular distribution including a set of controllable periodically distributed intensity maxima. In one or more embodiments, the cell period of the cellular field may be controlled/regulated in an arbitrary plane perpendicular to an axis of symmetry thereof.


Exemplary embodiments may, therefore, allow for dosated (e.g., through laser) influence on ensembles of micro-objects (e.g., micro-particles) in microtechnology and nanotechnology applications as discussed above in the Background section. Referring back to FIG. 1, a sample 124 (e.g., micro-particles) may be placed (e.g., in a sample holder 122) such that particles of sample 124 are configured to interact with the gradient light field to be influenced thereby; in other words, sample 124 may be placed between glass prism 108 and microscope 110. In one example embodiment, sample holder 122 may be a cuvette; it should be noted that sample holder 122 may be made of various types of materials (e.g., glass). In one or more embodiments, sample holder 122 may/may not serve to shape the gradient light field.



FIG. 7 shows a process flow diagram detailing the operations involved in controlling microparticles through a light field having controllable intensity and periodicity of maxima thereof, according to one or more embodiments. In one or more embodiments, operation 702 may involve providing a capability to control divergence of a coherent light beam having an axially symmetrical distribution of intensity thereof through optical divergence controller 106. In one or more embodiments, operation 704 may involve directing an output of optical divergence controller 106 related to the controlled divergence of the coherent light beam onto glass prism 108. In one or more embodiments, glass prism 108 may include a planar shape onto which a pyramidal structure is formed.


In one or more embodiments, glass prism 108 may be positioned such that the output of optical divergence controller 106 is incident on a planar surface of the planar shape or the pyramidal structure. In one or more embodiments, operation 706 may involve controlling a distance between maxima of an output light field of glass prism 108 and intensity thereof through controlling the divergence of the coherent light beam through optical divergence controller 106 and/or varying a distance between optical divergence controller 106 and glass prism 108. In one or more embodiments, operation 708 may then involve utilizing the output light field of glass prism 108 in controlling microparticles in a microtechnology or a nanotechnology application.


Although the present embodiments have been described with reference to specific example embodiments, it will be evident that various modifications and changes may be made to these embodiments without departing from the broader spirit and scope of the various embodiments. Accordingly, the specification and drawings are to be regarded in an illustrative rather than a restrictive sense.

Claims
  • 1. An optical device comprising: a laser source;a telescope collimator in an optical path immediately following the laser source to form a collimated coherent light beam having an axially symmetrical distribution of intensity thereof;an optical divergence controller in an optical path immediately following the telescope collimator to provide a capability to control divergence of the collimated coherent light beam; anda glass prism including a planar shape onto which a pyramidal structure is formed, the glass prism being positioned in an optical path immediately following the optical divergence controller such that an output of the optical divergence controller is incident on one of a planar surface of the planar shape and the pyramidal structure,wherein at least one of: controlling the divergence of the collimated coherent light beam through the optical divergence controller and varying a distance between the optical divergence controller and the glass prism enables controlling a distance between maxima of an output light field of the glass prism and intensity thereof,wherein the output light field of the glass prism is configured to be utilized in controlling microparticles in one of a microtechnology and a nanotechnology application, the microparticles being configured to be placed as part of a sample within a sample holder in an optical path immediately following the glass prism.
  • 2. The optical device of claim 1, wherein the optical divergence controller is a spherical lens with varying focal distance.
  • 3. The optical device of claim 1, further comprising at least one of a microscope and a CCD camera to at least one of observe, register and investigate the output light field of the glass prism.
  • 4. The optical device of claim 1, wherein the output light field of the glass prism is configured to be utilized to allow for dosated laser influence on ensembles of the microparticles.
  • 5. An optical system comprising: a laser source;a telescope collimator in an optical path immediately following the laser source to form a collimated coherent light beam having an axially symmetrical distribution of intensity thereof;an optical divergence controller in an optical path immediately following the telescope collimator to provide a capability to control divergence of the collimated coherent light beam;a glass prism including a planar shape onto which a pyramidal structure is formed, the glass prism being positioned in an optical path immediately following the optical divergence controller such that an output of the optical divergence controller is incident on one of a planar surface of the planar shape and the pyramidal structure; andan ensemble of microparticles as part of a sample within a sample holder in an optical path immediately following the glass prism,wherein at least one of: controlling the divergence of the collimated coherent light beam through the optical divergence controller and varying a distance between the optical divergence controller and the glass prism enables controlling a distance between maxima of an output light field of the glass prism and intensity thereof, andwherein the output light field of the glass prism is configured to be utilized in controlling the ensemble of microparticles.
  • 6. The optical system of claim 5, wherein the optical divergence controller is a spherical lens with varying focal distance.
  • 7. The optical system of claim 5, further comprising at least one of a microscope and a CCD camera to at least one of observe, register and investigate the output light field of the glass prism.
US Referenced Citations (186)
Number Name Date Kind
3160696 Gamo Dec 1964 A
3808550 Ashkin Apr 1974 A
4623930 Oshima et al. Nov 1986 A
4630184 Ferrero Dec 1986 A
4710817 Ando Dec 1987 A
4759628 Tatsuno et al. Jul 1988 A
4979221 Perryman et al. Dec 1990 A
5021854 Huth Jun 1991 A
5157473 Okazaki Oct 1992 A
5198660 Yokoyama et al. Mar 1993 A
5212382 Sasaki et al. May 1993 A
5262871 Wilder et al. Nov 1993 A
5301240 Stockum et al. Apr 1994 A
5308976 Misawa et al. May 1994 A
5363190 Inaba et al. Nov 1994 A
5412422 Yamada et al. May 1995 A
5448056 Tsuruta Sep 1995 A
5467128 Yates et al. Nov 1995 A
5468954 Furukawa Nov 1995 A
5557542 Asahina et al. Sep 1996 A
5565915 Kindo et al. Oct 1996 A
5631704 Dickinson et al. May 1997 A
5650643 Konuma Jul 1997 A
5665959 Fossum et al. Sep 1997 A
5705807 Throngnumchai et al. Jan 1998 A
5708471 Okumura Jan 1998 A
5754690 Jackson et al. May 1998 A
5777669 Uwatoko et al. Jul 1998 A
5841126 Fossum et al. Nov 1998 A
5892541 Merrill Apr 1999 A
5923369 Merrill et al. Jul 1999 A
5978025 Tomasini et al. Nov 1999 A
6028300 Rhoads et al. Feb 2000 A
6078037 Booth, Jr. Jun 2000 A
6115065 Yadid-Pecht et al. Sep 2000 A
6118482 Clark et al. Sep 2000 A
6130423 Brehmer et al. Oct 2000 A
6130713 Merrill Oct 2000 A
6157016 Clark et al. Dec 2000 A
6181375 Mitsui et al. Jan 2001 B1
6236449 Tanitsu May 2001 B1
6248990 Pyyhtiä et al. Jun 2001 B1
6282028 Waibel et al. Aug 2001 B1
6297488 Beraldin et al. Oct 2001 B1
6330030 O'Connor Dec 2001 B1
6359274 Nixon et al. Mar 2002 B1
6366312 Crittenden Apr 2002 B1
6476864 Borg et al. Nov 2002 B1
6580454 Perner et al. Jun 2003 B1
6587145 Hou Jul 2003 B1
6603607 Matsui et al. Aug 2003 B2
6631022 Kihira et al. Oct 2003 B1
6633028 Fowler Oct 2003 B2
6633335 Kwon et al. Oct 2003 B1
6677996 Chung et al. Jan 2004 B1
6735072 Liao May 2004 B2
6825936 Metcalfe et al. Nov 2004 B2
6831263 Skurnik et al. Dec 2004 B2
6873282 Murphy Mar 2005 B1
6884982 Beusch Apr 2005 B2
6909462 Shinotsuka et al. Jun 2005 B1
6927433 Hynecek Aug 2005 B2
6927796 Liu et al. Aug 2005 B2
6972795 Etoh et al. Dec 2005 B1
6977685 Acosta-Serafini et al. Dec 2005 B1
6982403 Yang et al. Jan 2006 B2
7053947 Sohn May 2006 B2
7115963 Augusto et al. Oct 2006 B2
7126838 Koizumi et al. Oct 2006 B2
7205522 Krymski Apr 2007 B2
7233350 Tay Jun 2007 B2
7245250 Kalayeh Jul 2007 B1
7262402 Niclass et al. Aug 2007 B2
7277129 Lee Oct 2007 B1
7280221 Wei Oct 2007 B2
7286174 Weale et al. Oct 2007 B1
7319423 Augusto et al. Jan 2008 B2
7319486 Shinotsuka Jan 2008 B2
7324146 Kanai Jan 2008 B2
7391004 Takashima et al. Jun 2008 B2
7426036 Feldchtein et al. Sep 2008 B2
7466429 de Groot et al. Dec 2008 B2
7483058 Frank et al. Jan 2009 B1
7502107 Mohanty et al. Mar 2009 B2
7504616 Nakamura et al. Mar 2009 B2
7522288 de Groot Apr 2009 B2
7547872 Niclass et al. Jun 2009 B2
7593651 Nicholls et al. Sep 2009 B2
7598998 Cernasov et al. Oct 2009 B2
7619674 Han et al. Nov 2009 B2
7623173 Nitta et al. Nov 2009 B2
7626624 Fraenkel et al. Dec 2009 B2
7696463 Kamiyama Apr 2010 B2
7697051 Krymski Apr 2010 B2
7701499 Barnea et al. Apr 2010 B2
7718953 Prather et al. May 2010 B2
7728893 Kagawa et al. Jun 2010 B2
7795650 Eminoglu et al. Sep 2010 B2
7847846 Ignjatovic et al. Dec 2010 B1
7858917 Stern et al. Dec 2010 B2
7868665 Tumer et al. Jan 2011 B2
7889355 de Lega et al. Feb 2011 B2
7911520 Shigematsu et al. Mar 2011 B2
7940317 Baxter May 2011 B2
7956912 Berezin Jun 2011 B2
7999945 Zara Aug 2011 B2
8026471 Itzler Sep 2011 B2
8077328 Scheibengraber et al. Dec 2011 B2
8089036 Manabe Jan 2012 B2
8089522 Choi et al. Jan 2012 B2
8093624 Renzi et al. Jan 2012 B1
8107290 Lee et al. Jan 2012 B2
8120687 Nishino et al. Feb 2012 B2
8126677 de Groot et al. Feb 2012 B2
8338773 Eldesouki et al. Dec 2012 B2
8405038 Bouhnik et al. Mar 2013 B2
8408034 Ishihara et al. Apr 2013 B2
8410416 Eldesouki et al. Apr 2013 B2
8426797 Aull et al. Apr 2013 B2
8462248 Berezin Jun 2013 B2
8471750 Rogers et al. Jun 2013 B2
8471895 Banks Jun 2013 B2
8531566 Cieslinski Sep 2013 B2
8564785 Newbury et al. Oct 2013 B2
8570421 Okada et al. Oct 2013 B2
8587697 Hussey et al. Nov 2013 B2
8587709 Kawahito et al. Nov 2013 B2
8619168 Choi et al. Dec 2013 B2
8653435 Eldesouki Feb 2014 B2
8665342 Al-Salem et al. Mar 2014 B2
8785831 Krymski Jul 2014 B2
8829409 Wadsworth Sep 2014 B2
20010030277 Rhoads Oct 2001 A1
20010052941 Matsunaga et al. Dec 2001 A1
20020024058 Marshall et al. Feb 2002 A1
20030010896 Kaifu et al. Jan 2003 A1
20030103212 Westphal et al. Jun 2003 A1
20030193771 Liao Oct 2003 A1
20040058553 Tanaka Mar 2004 A1
20040189999 De Groot et al. Sep 2004 A1
20040243656 Sung et al. Dec 2004 A1
20050012033 Stern et al. Jan 2005 A1
20050248675 Hashimoto et al. Nov 2005 A1
20060044451 Liang et al. Mar 2006 A1
20060131480 Charbon et al. Jun 2006 A1
20060131484 Peting Jun 2006 A1
20060175529 Harmon et al. Aug 2006 A1
20060231742 Forsyth Oct 2006 A1
20060245071 George et al. Nov 2006 A1
20070022110 Suda et al. Jan 2007 A1
20070084986 Yang et al. Apr 2007 A1
20080106603 Whitehead et al. May 2008 A1
20080230723 Tanaka et al. Sep 2008 A1
20080231339 Deschamps Sep 2008 A1
20080252762 Iwamoto et al. Oct 2008 A1
20080279441 Matsuo et al. Nov 2008 A1
20090182528 de Groot et al. Jul 2009 A1
20090244971 Lee et al. Oct 2009 A1
20090256735 Bogaerts Oct 2009 A1
20100026838 Belenky et al. Feb 2010 A1
20100181491 Karim et al. Jul 2010 A1
20100182011 Prescher et al. Jul 2010 A1
20100204459 Mason et al. Aug 2010 A1
20100213353 Dierickx Aug 2010 A1
20100245809 Andreou et al. Sep 2010 A1
20100270462 Nelson et al. Oct 2010 A1
20100271517 De Wit et al. Oct 2010 A1
20100315709 Baer Dec 2010 A1
20110017918 Baeumer et al. Jan 2011 A1
20110090385 Aoyama et al. Apr 2011 A1
20110188120 Tabirian et al. Aug 2011 A1
20110249148 Prescher et al. Oct 2011 A1
20110260039 Fowler Oct 2011 A1
20120056078 Eldesouki et al. Mar 2012 A1
20120057059 Eldesouki et al. Mar 2012 A1
20120057152 Eldesouki et al. Mar 2012 A1
20120091324 Grund Apr 2012 A1
20120113252 Yang et al. May 2012 A1
20120138774 Kelly et al. Jun 2012 A1
20120229669 Okada et al. Sep 2012 A1
20130057945 Ueno et al. Mar 2013 A1
20130068928 Eldesouki et al. Mar 2013 A1
20130094030 Sherif et al. Apr 2013 A1
20130135486 Wan May 2013 A1
20130168535 Eldesouki Jul 2013 A1
20140097329 Wadsworth Apr 2014 A1
Foreign Referenced Citations (13)
Number Date Country
202048982 Nov 2011 CN
0451852 Oct 1991 EP
1041637 Oct 2000 EP
1104178 May 2001 EP
1148348 Oct 2001 EP
9918717 Apr 1999 WO
2005069040 Jul 2005 WO
2007043036 Apr 2007 WO
20081511155 Dec 2008 WO
2009042901 Apr 2009 WO
2009115956 Sep 2009 WO
2010124289 Oct 2010 WO
2013105830 Jul 2013 WO
Non-Patent Literature Citations (16)
Entry
Ryzhevich, A., et al., “Application of Ring Laser Fields for Microstructures Creation,” Nonlinear Phenomena in Complex Systems vol. 14, No. 3 (Nov. 2011).
“Applications of ring laser fields for microstructure creation”, Nonlinear Pnenomeno In Complex Systems, vol. 14, No. 3, Nov. 2011 by Anatol Ryzhevich et al. (p. 1) http://www.j-npcs.org/abstracts/vol2011/v14no3/v14no3p236.html.
“A 4M Pixel CMOS Image Sensor for High Speed Image Capture”, P. Donegan et al. (pp. 4), Dec. 2005.
“A CMOS image sensor for high-speed imaging”, IEEE Xplore—Digital Library, 2000 by Stevanovic, N. et al (p. 1) http://ieeexplore.ieee.org/xpl/articleDetails.jsp?tp=&arnumber=839710&url=http%3A%2F%2Fieeexplore.ieee.org%2Fxpls%2Fabs—all.jsp%3Farnumber%3D839710, Feb. 2000.
“Fast Model-Free Super-Resolution Using a Two-Sensor Camera”, Techtransfer, University of Michigan by Andrew Yagle (p. 1), Dec. 2014, http://inventions.umich.edu/technologies/4806—fast-model-free-super-resolution-using-a-two-sensor-camera.
Design and characterization of ionizing radiation-tolerant CMOS APS image sensors up to 30 Mrd (SI) total dose, Nuclear Science, IEEE Xplore Digital Library, vol. 48, Issue 6, Dec. 2001 by EI-Sayed EID et al. (p. 1) http://ieeexplore.ieee.org/xpl/articleDetails.jsp?tp=&arnumber=983133&url=http%3A%2F%2Fieeexplore.ieee.org% 2Fxpls%2Fabs all.isp%3Farnumber%3D983133.
“Spatial speckle correlometry in applications to tissue structure monitoring”, ResearchGate, Applied Optics, vol. 36, Issue 22, 1997 by D. A. Zimnyakov et al. (p. 1) Sep. 1997 http://www.researchgate.net/ publication/5593616 Spatial speckle correlometry in applications to tissue structure monitori.
“Integrated CMOS Sensors for Fluorescence Spectroscopy and Imaging”, ResearchGate, Nov. 2009 by Munir Ei-Desouki et al. (p. 1) http://www.researchgate.net/ publication/249653851 Integrated CMOS Sensors for Fluorescence Spectroscopy and Imaging.
“Applications of ring laser fields for microstructure creation”, Nonlinear Pnenomena in Complex Systems, vol. 14, No. 3, Nov. 2011 by Anatol Ryzhevich et al. (p. 1) http://www.j-npcs.org/abstracts/vol2011/v14no3/v14no3p236.html.
“A CMOS Active Pixel Image Sensor with In-pixel CDS for High-Speed Cameras”, Jan. 17, 2004 by Toru Inoue et al. (8 pages) http://www.photron.com/whitepapers/a%20CMOS%20Active%20Pixel%201mage%20Sensor%20with%201n-pixel% 20CDS%20for%20Hidh-Speed%20Cameras.pdf.
“Miniature endoscope for simultaneous optical coherence tomography and laser-induced fluorescence measurement”, Applied Optics, vol. 43, No. 1, Jan. 1, 2004 by Alexandre R. Tumlinson et al. (9 pages) http://www2.engr.arizona.edu/˜bmeoptics/papers/Miniatureendoscope.pdf.
“CMOS Active-Pixel Sensor With In-Situ Memory for Ultrahigh-Speed Imaging”, ResearchGate, Jul. 2011 by M.M. ElDesouki et al. (1 page) http://www.researchgate.net/publication/224184430—CMOS—Active-Pixel—Sensor—Withi—In- Situ Memory for Ultrahigh-Speed Imaging.
“A 4M Pixel CMOS Image Sensor for High Speed Image Capture”, P. Donegan et al. (4 pages) Dec 2005.
“A CMOS image sensor for high-speed imaging”, IEEE Xplore—Digital Library, 2000 by Stevanovic, N. et al. (1 pages) http://ieeexplore.ieee.org/xpl/articleDetails.jsp?tp=&arnumber=839710&url=http%3A%2F%2Fieeexplore.ieee.org% 2Fxpls%2Fabs—all.jsp%3Farnumber%3D839710 Feb 2000.
“Ultra-High-Speed Image Signal Accumulation Sensor,” sensors, 2010 by Takeharu Goji Etoh et al. (Page 12) Apr. 2010.
“Fast Model-Free Super-Resolution Using a Two-Sensor Camera”, Techtransfer, University of Michigan by Andrew Yagle (p. 1) published No. later than Dec. 2014 http://inventions.umich.edu/technologies/4806fast-model-free-super-resolution-using-a-two-sensor-camera.
Related Publications (1)
Number Date Country
20130099108 A1 Apr 2013 US