The embodiments described herein relate generally to endoscopic scanning methods and apparatus and, more particularly, to a photoacoustic endoscope that enables both photoacoustic imaging and ultrasonic imaging through the use of a rotatable reflector, such as a prism or a mirror.
Photoacoustic microscopy or computed tomography is an emerging imaging modality that has much potential for in vivo structural and functional imaging of biological tissues. It can produce spectroscopic optical absorption-based contrast images in optically scattering media such as human tissue while maintaining high spatial resolution (up to approximately 10 μm). In addition to the intrinsic contrast, by employing other biocompatible molecular contrast agents, such as organic dyes, quantum dots, or nano-particles, lesions can be profiled with molecular contrasts at high resolution.
Photoacoustic waves are generated by the instant thermal stress of biological tissue induced by an external energy supply, typically through a laser pulse although radiofrequency or microwave pulses may also be used. Even with weak light illumination, less than the ANSI safety limit (20 mJ/cm2 per laser pulse), detectable acoustic waves can be generated by the photoacoustic phenomenon, and cross-sectional or volumetric images of internal structures can be reconstructed by moving the illumination and detection points over the region of interest. To acquire the photoacoustic signal, typically a light delivering unit, a signal detection unit including an ultrasonic transducer, and a mechanical scanning unit are employed.
In one aspect, a reflection-mode photoacoustic endoscope is provided, including a tube, a light source configured to emit a light pulse suitable for photoacoustic imaging, an ultrasonic transducer configured to detect a response signal, and a light and acoustic reflector rotatable relative to the tube.
In another aspect, a reflection-mode photoacoustic endoscope is provided, including a light source configured to emit a light pulse, a signal detection or transmission unit configured to receive or emit an ultrasonic pulse, and a rotatable or scanning reflector configured to reflect the light pulse and the ultrasonic pulse into a target area of an object, and reflect a response signal to the signal detection unit. The response signal is one of a photoacoustic wave generated by the object responsive to the light pulse and an ultrasonic pulse echo generated by the object responsive to the ultrasonic pulse.
In another aspect, an endoscopy system is provided, including a reflection-mode photoacoustic endoscope, a data-acquisition system, and a data-analysis computer. The endoscope includes a light source configured to emit a light pulse, a signal detection or transmission unit configured to receive or emit an ultrasonic pulse, and a rotatable reflector configured to reflect the light pulse and the ultrasonic pulse into a target area of an object, and reflect a response signal to the signal detection unit. The response signal is one of a photoacoustic wave generated by the object responsive to the light pulse and an ultrasonic echo generated by the object responsive to the ultrasonic pulse. The data-acquisition system is configured to receive an electronic signal generated by the signal detection unit based on the response signal, and the data-analysis computer is configured to generate an image based on the electronic signal.
In another aspect, an endoscopy scanning method includes emitting a pulse, reflecting the pulse into an object using a rotatable mirror such that a response signal is emitted by the object responsive to the incident pulse, and reflecting the response signal, by the mirror, to a signal detection unit. The pulse is one of a light pulse and an ultrasonic pulse, and the response signal is one of a photoacoustic wave generated by the object in response to the light pulse and an ultrasonic echo generated by the object in response to the ultrasonic pulse. The method also includes generating an electronic signal based on the response signal, and generating an image based on the electronic signal.
The embodiments described herein may be better understood by referring to the following description in conjunction with the accompanying drawings.
While the making and using of various embodiments of the present invention are discussed in detail below, it should be appreciated that the present invention provides many applicable inventive concepts that can be embodied in a wide variety of specific contexts. The specific embodiments discussed herein are merely illustrative of specific ways to make and use the invention and do not delimit the scope of the invention.
To facilitate the understanding of the embodiments described herein, a number of terms are defined below. The terms defined herein have meanings as commonly understood by a person of ordinary skill in the areas relevant to the present invention. Terms such as “a,” “an,” and “the” are not intended to refer to only a singular entity, but rather include the general class of which a specific example may be used for illustration. The terminology herein is used to describe specific embodiments of the invention, but their usage does not delimit the invention, except as outlined in the claims.
To be consistent with the commonly used terminology, whenever possible, the terms used herein will follow the definitions recommended by the Optical Society of America (OCIS codes).
In some embodiments, the term “photoacoustic microscopy” refers generally to a photoacoustic imaging technology that detects pressure waves generated by light absorption in the volume of a material (such as biological tissue) and propagated to the surface of the material. In other words, photoacoustic microscopy is a method for obtaining three-dimensional images of the optical contrast of a material by detecting acoustic or pressure waves traveling from the object. The emphasis is on the micrometer scale image resolution.
In some embodiments, the term “photoacoustic tomography” also refers to a photoacoustic imaging technology that detects acoustic or pressure waves generated by light absorption in the volume of a material (such as biological tissue) and propagated to the surface of the material. The emphasis is sometimes on photoacoustic computed tomography, i.e., cross-sectional or three-dimensional photoacoustic imaging based on computer reconstruction, although the most general definition of photoacoustic tomography encompasses photoacoustic microscopy.
In some embodiments, the term “ultrasonography” refers generally to the conventional ultrasound pulse-echo imaging.
In some embodiments, the term “reflection mode” refers generally to the operation mode of a photoacoustic imaging system that detects pressure waves transmitted from the volume of their generation to the optical irradiation surface.
In some embodiments, the term “pulse-echo mode” refers generally to a scanning mode used to acquire A-line signals by detecting the amplitude of the backscattered echoes versus the time after transmission of the ultrasound pulse.
In some embodiments, the term “dark-field illumination” refers generally to an illumination method in photoacoustic microscopy, which is the opposite of bright-field illumination. By illuminating a target tissue at a low angle from the side, over a broad area having an annular shape, strong photoacoustic signal generation from the superficial surface above the focal zone of acoustic lens may be avoided or minimized.
In some embodiments, the term “photoacoustic waves” refers generally to pressure waves produced by light absorption.
In some embodiments, the term “time-resolved detection” refers generally to the recording of the time history of a pressure wave.
In some embodiments, the term “A-line” (“A” stands for amplitude) originates from the terminology of traditional ultrasonography, and it refers generally to a one-dimensional image along the depth direction. Here, the A-line is plotted with the acquired time-resolved photoacoustic signals versus the time after the launch of the light pulses.
In some embodiments, the term “B-scan” or “B-mode” (“B” stands for brightness) refers generally to a mechanical or electronic scanning mode that produces a two-dimensional image showing a cross section of tissue. Each line perpendicular to the scanning direction in the image represents an A-line, with the brightness of the signal being proportional to the amplitude of the photoacoustic signal.
In some embodiments, the term “piezoelectric detector” refers generally to detectors of acoustic waves utilizing the principle of electric charge generation upon a change of volume within crystals subjected to a pressure wave.
In some embodiments, the term “transducer array” refers generally to an array of ultrasonic transducers.
In some embodiments, the terms “focused ultrasonic detector,” “focused ultrasonic transducer,” and “focused piezoelectric transducer” refer generally to a curved ultrasonic transducer with a hemispherical surface or a planar ultrasonic transducer with an acoustic lens attached or an electronically focused ultrasonic array transducer.
In some embodiments, the terms “transducer array” and “phase array transducer” refer generally to an array of piezoelectric ultrasonic transducers.
In some embodiments, the term “mirror” refers generally to any device capable of deflecting propagation axis light and/or ultrasound. Such a device may include a metal or dielectric angle mirror, off-axis spherical or parabolic mirror, prism, lens, or any combination thereof.
Minimally invasive tissue diagnosis via an endoscope has shown broad applicability in the medical imaging field. Ultrasonography based imaging catheters have become widely used, and have shown robust performance independently or in combination with video endoscopes. Unlike the video endoscope, ultrasonographic endoscopes enable the diagnosis of deeper areas of the organ wall. However, they have relatively poor contrast and are thus not best suited, for example, for detecting early stage cancer. To overcome this shortcoming, optical imaging modalities have been developed and are attracting much attention due to their advantages in contrast, safety, and portability. Recent studies have shown their potential and superiority over conventional ultrasonography in the early diagnosis of cancerous tissue. The endoscopic optical coherence tomographic (OCT) imaging technique shows much potential in terms of optical contrast and resolution. This technique also has the advantage of realizing a very tiny catheter probe with high scanning speed. However, its poor imaging depth (less than 1 mm) still remains a major limitation.
In at least some known medical imaging, optical modalities provide an optical contrast image. However, such optical modalities are fundamentally limited to poor spatial resolution at depths greater than one transport mean free path (e.g., ˜1 mm in most biological tissues) due to high optical scattering in tissue. For example, diffuse optical tomography (DOT) may produce tomographic images reaching regions up to several centimeters deep, but it is very poor in spatial resolution because diffused (scattered) light is employed. A main application for DOT is imaging the human brain and/or breast. However, DOT is inappropriate for endoscopic applications.
Further examples are endoscopic optical techniques that employ ballistic or quasi-ballistic photons, such as confocal endoscopy. Endoscopic optical and optical coherence tomographic (OCT) probes having various components and scanning mechanisms have been reported. However, while such techniques and/or probes are capable of imaging small objects with high resolution, they are still unsatisfactory in detecting cancerous tissue developed deeper than one transport mean free path below the surface.
In addition, ultrasonography may also be miniaturized for endoscopic diagnosis. This imaging modality takes advantage of high resolution and deep penetration characteristics of ultrasonic waves. Owing to the low scattering of ultrasound, compared to that of light in biological tissue, deep imaging may be achieved. During scanning, pulsed ultrasonic waves are sent to a region of interest, and reflected waves, or echoes, are recorded and reconstructed as a cross-sectional, e.g., B-scan, image or as a 3-D volumetric image. However, this technique has insufficient contrast because the mechanical properties of the early-stage abnormal tissue differ little from those of normal tissue.
Photoacoustic imaging modalities capitalize on two domains, i.e., imaging of optical contrast through light illumination, and deep imaging with high resolution by employing photoacoustically induced ultrasonic waves. For this reason, photoacoustic imaging technology is considered one of the most promising imaging modalities for biomedical applications. Its endoscopic realization in particular can make significant contributions to the medical imaging field.
In realizing a catheter probe for photoacoustic endoscopy, the size restriction is a most challenging issue. Among known endoscopic imaging modalities, two imaging systems are representative and related to the embodiments described herein. The first is an ultrasonic endoscopic catheter, and the second is an optical catheter probe employing optical coherence tomography. The ultrasonic endoscopic catheter captures a reflected signal from a region of interest after sending an ultrasonic pulse, which is referred to as the pulse-echo mode. The optical catheter probe employs a backscattered optical signal from a focused illumination. In order to produce a circular B-scan image, both systems use circumferential sector scanning, or radial scanning, with a scanning element, such as a focused ultrasonic transducer or optical lens, attached at the tip of a flexible shaft. If necessary, linear motion of the scanning element, which is referred to as pull-back, may be accomplished manually or automatically to acquire successive B-scan images, which are necessary for volumetric image composition. The required mechanical driving force is typically transmitted from the proximal end through a flexible shaft embedded in the inner part of the catheter. The electrical signal from the ultrasonic transducer (in the case of endoscopic ultrasonography) or the optical signal (in the case of endoscopic OCT) from the optical lens is transferred to the signal-receiving center through electromagnetic or optical coupling at the proximal end and finally reconstructed as a B-scan or volumetric image. This is the most widely utilized scanning mechanism because it can be fabricated with a very simple structure in restricted space. Such endoscopic probes can work separately as intravascular probes or jointed with video endoscopes through the instrument channels. In addition, such a scanner shows robust performance in terms of scanning speed, e.g., more than 30 Hz frame rate for B-scan, as well as flexibility in advancing toward the region of interest in the tissue. However, in using endoscopic probes, it is technically difficult to transmit both the impulse energy, whether the energy is an optical or electrical pulse, and the resultant response signal from a target through the rotating proximal end. This disjointed transmission mechanism deteriorates signal stability during rotational motion and worsens the signal-to-noise ratio as well. This issue would become more serious in a photoacoustic endoscope system because the induced signal from the photoacoustic phenomenon is weaker than that of conventional ultrasonographic endoscopes using the pulse-echo method. For this reason, more stable light delivery and photoacoustic signal transfer during scanning are essential in realizing the system. Additionally, the relatively high stiffness of the flexible shaft limits the endoscope's abilities, e.g., maneuverability, in imaging delicate tissues. Hereinafter, embodiments of a scanning mechanism and system configuration for the effective embodiment of a photoacoustic endoscope are disclosed.
Addressing this limitation, the embodiments described herein provide a photoacoustic endoscope, which is a hybrid imaging modality combining the strengths of two domains, optics and ultrasound. Since it is capable of producing optical absorption-based contrast images at challenging depths (1-5 mm) with high spatial resolution, it is superior in screening suspicious tissue at deeper regions. Moreover, the described system in accordance with the current invention is capable of producing double contrast images having different origins, i.e., an optical absorption based image and a pure ultrasound image based on the tissue's acoustic properties. The spectral behavior of optical absorption in the region of interest enables analysis of metabolism and offers rich information concerning the tissue. In addition, when used with appropriate biochemical markers for a specific disease, the embodiments described herein facilitate identifying tissue abnormalities more clearly.
The embodiments described herein may be used in the diagnosis of various tissue lesions that develop in internal organs. Its applicability lies in various organs and many duct structures, such as the lungs, esophagus, gastrointestinal tract, colon, or blood vessels. Most of all, it is expected to be especially useful in screening cancerous tissues, such as myogenic tumors of the esophagus, gastric cancer, pancreatic cancer, colon cancer and carcinoma of the common bile duct. Needless to say, in addition to its medical applications for human welfare, it can be applied to various types of animal study for research purposes.
Such a configuration facilitates stable light delivery and stable signal detection, which means improvement of the SNR. Because the illumination optics 103 and ultrasonic detection element 105 (with the acoustic lens 104) do not participate in the mechanical scanning but remain static, possible technical issues in disjointed rotating coupling, i.e., light transfer to and signal reception from the proximal end of the rotating flexible shaft, may be avoided. Here, “static” does not mean the preclusion of the movement of the elements with the whole probe system. Rather, “static” means no relative movement in the distal end. Additionally, since this scanning mechanism does not preclude traditional pure ultrasonic imaging capability, i.e., pulse-echo mode, two forms of imaging can be performed and automatically co-registered for side-by-side displays and/or overlays. This scanning mechanism's simple structure permits fabrication of a tiny endoscopic probe, one small enough to perform not only independently but also with existing gastrointestinal fiber scopes through their instrument channels.
Since the mirror's oblique reflection surface serves as a signal transmitter as well as a scanning substitute, its surface must be made with an appropriate material for both light and ultrasonic wave reflection. From basic acoustic theory, one of ordinary skill in the art should understand that ultrasound rays, both longitudinal rays and shear rays, approaching the reflection surface of high acoustic impedance material at a large incidence angle are highly or totally reflected. Because of the high acoustic impedance difference between the scanning mirror 115 and its background medium (i.e., immersion medium) 101, the ultrasonic reflection from the mirror 115 is high even at small incidence angles. Therefore, the acoustic wave reflection mechanism of the present invention, i.e., using a scanning mirror having an oblique reflection surface, facilitates providing satisfactory propagation of ultrasonic waves, which is comparable to the conventional ultrasonographic endoscope system that directly rotates the detection element. In the exemplary embodiment, the inner part of the distal end is filled with an acoustically transparent liquid medium 101, such as water or mineral oil, to provide an acoustic impedance matching medium for ultrasonic wave propagation. In addition, in the exemplary embodiment, the optically transparent imaging window 116 is made with an ultrasound permeable material, and its area is determined according to its specific application. Instead of attaching an acoustic lens 104 having a concave surface to the ultrasonic transducer 105, the reflection surface of the scanning mirror 115 may be formed as a curved shape like a concave optical mirror to focus ultrasonic waves. In some embodiments, the scanning mirror 115 is formed with a parabolic shape in order to minimize aberration. In the exemplary embodiment, an array of ultrasonic transducers may replace the acoustic lens 104 and provide spatial focusing capability using synthetic aperture imaging. The ultrasonic sensing element 105 may be composed of various materials, forms, and/or types, such as piezo-polymer or piezoceramic, focused or unfocused, and single element or an array of many elements. It is desirable to have broad bandwidth for achieving high axial resolution. Typical endoscopic ultrasonographic imaging frequencies range from a few megahertz (MHz) to approximately 100.0 MHz. A PVDF film based transducer is also good for acoustic wave detection. In addition, optical detection methods, such as the Fabry-Perot interferometery, may replace the conventional piezoelectric effect based transducers. In some embodiments, in order to increase the electric signal transmission efficiency from the ultrasonic transducer 105 to the detection electronics 109, a preamplifier circuit is embedded into the catheter tube near the ultrasonic transducer 105.
Maintaining the aforementioned scanning concept shown in
The micromotor based scanning mechanism has several advantages over the conventional method utilizing a flexible shaft. It improves catheter flexibility, which means better maneuverability, and does not require rotational coupling of optical and electric signals thus improves the SNR of the system. Moreover, any kink in the endoscope's body would not affect the scanning mirror's movement, and a phase delay in the rotation of the scanning mirror would not occur, but it might when a flexible shaft is employed. In various embodiments, the configuration of the required elements may be varied for specific applications, as described hereinbelow.
The current system provides photoacoustic and conventional ultrasonic imaging simultaneously according to the aforementioned method and may be used for diagnostic, monitoring, or research purposes. In addition, this scanning mechanism and related imaging systems according to the present invention may replace or complement conventional planar (both in x and y-direction) scanning mode based photoacoustic imaging systems. The scanning mechanism may be realized as a co-operating probe with a video endoscope system, being small enough to be pulled through the instrument channel (around 2.7 mm) of the video endoscope. In addition, the current photoacoustic endoscope system may be used for diagnosis independently as a specialized gastro-endoscope or recto-scope. In this case, the probe diameter is equal or close to the body size of conventional video endoscopes, around 10 mm in diameter. Such a probe may incorporate an ultrasound preamplifier for improving SNR, angulation capability for probe steering, and a CCD camera for transmitting visual information during it maneuvers. To provide stable contact conditions between the endoscope and target tissues, the balloon contact or water immersion methods may be employed.
The main applications of the technology include, but are not limited to, in vivo imaging and diagnosis of various kinds of cancerous tissues in the gastrointestinal tract and plaques in blood vessels of humans. The present invention may use the spectral properties of intrinsic optical contrast to monitor blood oxygenation (oxygen saturation of hemoglobin), blood volume (total hemoglobin concentration), and/or the metabolic rate of oxygen consumption, which is referred to as functional imaging. It may also use the spectral properties of a variety of dyes or other contrast agents to obtain additional functional or molecular-specific information, i.e., molecular imaging. Since the acoustic property based contrast image supplied by the pure ultrasonic imaging capability is produced together with the photoacoustic image, plenty of diagnostic information may be provided to a practitioner synergistically.
Using the optical fiber illumination method shown in
In
In
Preserving the basic scanning concept shown in
In
In
In
Preserving the basic system configuration and scanning mechanism shown in
In
In
In the exemplary embodiment, the pulse induces the object to emit a response signal. If the pulse signal is a light pulse, the response signal is a photoacoustic wave. Alternatively, if the pulse signal is an ultrasonic pulse, the response signal is an ultrasonic pulse echo. The response signal is reflected 1103 by the mirror 115 to a signal detection unit that includes, for example, an acoustic lens 104 and an ultrasonic transducer 105. The signal detection unit generates 1104 an electronic signal based on the response signal and transmits the electronic signal to a data-acquisition system 205. Finally, a data-analysis computer 207 generates 1105 an image based on the electronic signal, for display to an operator.
As enumerated before, possible configurations for realizing photoacoustic endoscope systems were provided according to the current invention. There may be further alternatives with minor modifications of the associated elements, in their number, size, position, or replacement with equivalents. In addition, basic ideas provided by the embodiments shown in
It will be understood that the particular embodiments described herein are shown by way of illustration and not as limitations of the invention. The principal features of this invention may be employed in various embodiments without departing from the scope of the invention. Those of ordinary skill in the art will recognize numerous equivalents to the specific procedures described herein. Such equivalents are considered to be within the scope of this invention and are covered by the claims.
All of the compositions and/or methods disclosed and claimed herein may be made and/or executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of the embodiments included herein, it will be apparent to those of ordinary skill in the art that variations may be applied to the compositions and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit, and scope of the invention. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope, and concept of the invention as defined by the appended claims.
It will be understood by those of skill in the art that information and signals may be represented using any of a variety of different technologies and techniques (e.g., data, instructions, commands, information, signals, bits, symbols, and chips may be represented by voltages, currents, electromagnetic waves, magnetic fields or particles, optical fields or particles, or any combination thereof). Likewise, the various illustrative logical blocks, modules, circuits, and algorithm steps described herein may be implemented as electronic hardware, computer software, or combinations of both, depending on the application and functionality. Moreover, the various logical blocks, modules, and circuits described herein may be implemented or performed with a general purpose processor (e.g., microprocessor, conventional processor, controller, microcontroller, state machine or combination of computing devices), a digital signal processor (“DSP”), an application specific integrated circuit (“ASIC”), a field programmable gate array (“FPGA”) or other programmable logic device, discrete gate or transistor logic, discrete hardware components, or any combination thereof designed to perform the functions described herein. Similarly, steps of a method or process described herein may be embodied directly in hardware, in a software module executed by a processor, or in a combination of the two. A software module may reside in RAM memory, flash memory, ROM memory, EPROM memory, EEPROM memory, registers, hard disk, a removable disk, a CD-ROM, or any other form of storage medium known in the art. Although preferred embodiments of the present invention have been described in detail, it will be understood by those skilled in the art that various modifications can be made therein without departing from the spirit and scope of the invention as set forth in the appended claims.
A controller, computing device, or computer, such as described herein, includes at least one or more processors or processing units and a system memory. The controller typically also includes at least some form of computer readable media. By way of example and not limitation, computer readable media may include computer storage media and communication media. Computer storage media may include volatile and nonvolatile, removable and non-removable media implemented in any method or technology that enables storage of information, such as computer readable instructions, data structures, program modules, or other data. Communication media typically embody computer readable instructions, data structures, program modules, or other data in a modulated data signal such as a carrier wave or other transport mechanism and include any information delivery media. Those skilled in the art should be familiar with the modulated data signal, which has one or more of its characteristics set or changed in such a manner as to encode information in the signal. Combinations of any of the above are also included within the scope of computer readable media.
The embodiments described herein relate to a concurrent optical excitation and ultrasonic detection that scans an object with motion of a single element (mirror). A mirror serves three purposes: it is a moving scanning substitute, and it reflects both light to be delivered to the target tissue and ultrasonic waves received from the target. It enables object scanning similarly to a universal catheterized medical imaging device while maintaining the illumination optics and ultrasonic detection element stationary. Additionally, the employment of a micromotor for the rotation of the scanning mirror and/or other active scanning techniques enables a more simplified system that eliminates flexible shafts thus improving catheter flexibility and does not use rotational coupling of optical and electric signals thus improving the signal to noise ratio of the system. The system effectively positions the required illumination optical unit and facilitates performing photoacoustic imaging as well as conventional pure ultrasonic imaging. It thereby enables production of double contrasts based on acoustic properties and optical absorption properties, making it desirable for the characterization of tissue abnormalities such as tumors. Similarly, pure optical imaging such as confocal microscopy and optical coherence tomography can be incorporated for multi-modality imaging. By utilizing a strong magnetic coupler with the micromotor, the required rotational force may be transmitted to the mirror effectively without direct mechanical connection, which enables diverse variations in the configuration of the components.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims.
This application is a continuation application of U.S. patent application Ser. No. 13/143,832, filed Jul. 8, 2011, which is a 35 U.S.C. § 371 national stage application of PCT Application No. PCT/US2010/020488, filed Jan. 8, 2010, which claims the benefit of U.S. Provisional Patent Application No. 61/143,668 filed Jan. 9, 2009, the contents of which are hereby incorporated by reference in their entirety.
This invention was made with government support under grant R01 NS46214, awarded by the U.S. National Institutes of Health. The government has certain rights in the invention.
Number | Name | Date | Kind |
---|---|---|---|
4029756 | Gaafar | Jun 1977 | A |
4127318 | Determann et al. | Nov 1978 | A |
4255971 | Rosencwaig | Mar 1981 | A |
4267732 | Quate | May 1981 | A |
4375818 | Suwaki | Mar 1983 | A |
4385634 | Bowen | May 1983 | A |
4430897 | Quate | Feb 1984 | A |
4462255 | Guess et al. | Jul 1984 | A |
4468136 | Murphy et al. | Aug 1984 | A |
4489727 | Matsuo et al. | Dec 1984 | A |
4546771 | Eggleton et al. | Oct 1985 | A |
4596254 | Adrian et al. | Jun 1986 | A |
4740081 | Martens et al. | Apr 1988 | A |
4802461 | Cho | Feb 1989 | A |
4802487 | Martin et al. | Feb 1989 | A |
4809703 | Ishikawa et al. | Mar 1989 | A |
4850363 | Yanagawa | Jul 1989 | A |
4860758 | Yanagawa et al. | Aug 1989 | A |
4869256 | Kanno et al. | Sep 1989 | A |
4921333 | Brody et al. | May 1990 | A |
4995396 | Inaba et al. | Feb 1991 | A |
5070455 | Singer et al. | Dec 1991 | A |
5083549 | Cho et al. | Jan 1992 | A |
5107844 | Kami et al. | Apr 1992 | A |
5115814 | Griffith et al. | May 1992 | A |
5125410 | Misono et al. | Jun 1992 | A |
5140463 | Yoo et al. | Aug 1992 | A |
5170793 | Takano et al. | Dec 1992 | A |
5207672 | Roth et al. | May 1993 | A |
5227912 | Ho et al. | Jul 1993 | A |
5305759 | Kaneko et al. | Apr 1994 | A |
5320106 | Tanaka et al. | Jun 1994 | A |
5321501 | Swanson et al. | Jun 1994 | A |
5331466 | Van Saarloos | Jul 1994 | A |
5345938 | Nishiki et al. | Sep 1994 | A |
5373845 | Gardineer et al. | Dec 1994 | A |
5414623 | Lu et al. | May 1995 | A |
5445155 | Sieben | Aug 1995 | A |
5465722 | Fort et al. | Nov 1995 | A |
5506975 | Onodera | Apr 1996 | A |
5546947 | Yagami et al. | Aug 1996 | A |
5546948 | Hamm et al. | Aug 1996 | A |
5615675 | O'Donnell et al. | Apr 1997 | A |
5635784 | Seale | Jun 1997 | A |
5651366 | Liang et al. | Jul 1997 | A |
5713356 | Kruger | Feb 1998 | A |
5718231 | Dewhurst et al. | Feb 1998 | A |
5836872 | Kenet et al. | Nov 1998 | A |
5840023 | Oraevsky et al. | Nov 1998 | A |
5860934 | Sarvazyan | Jan 1999 | A |
5913234 | Julliard et al. | Jun 1999 | A |
5971998 | Russell et al. | Oct 1999 | A |
5991697 | Nelson et al. | Nov 1999 | A |
6055097 | Lanni et al. | Apr 2000 | A |
6102857 | Kruger | Aug 2000 | A |
6104942 | Kruger | Aug 2000 | A |
6108576 | Alfano et al. | Aug 2000 | A |
6111645 | Tearney et al. | Aug 2000 | A |
6134003 | Tearney et al. | Oct 2000 | A |
6216025 | Kruger | Apr 2001 | B1 |
6233055 | Mandella et al. | May 2001 | B1 |
6282011 | Tearney et al. | Aug 2001 | B1 |
6292682 | Kruger | Sep 2001 | B1 |
6309352 | Oraevsky et al. | Oct 2001 | B1 |
6341036 | Tearney et al. | Jan 2002 | B1 |
6379325 | Benett et al. | Apr 2002 | B1 |
6405069 | Oraevsky et al. | Jun 2002 | B1 |
6413228 | Hung et al. | Jul 2002 | B1 |
6421164 | Tearney et al. | Jul 2002 | B2 |
6432067 | Martin et al. | Aug 2002 | B1 |
6466806 | Geva et al. | Oct 2002 | B1 |
6485413 | Boppart et al. | Nov 2002 | B1 |
6490470 | Kruger | Dec 2002 | B1 |
6498942 | Esenaliev et al. | Dec 2002 | B1 |
6498945 | Alfheim et al. | Dec 2002 | B1 |
6501551 | Tearney et al. | Dec 2002 | B1 |
6564087 | Pitris et al. | May 2003 | B1 |
6567688 | Wang | May 2003 | B1 |
6626834 | Dunne et al. | Sep 2003 | B2 |
6633774 | Kruger | Oct 2003 | B2 |
6654630 | Zuluaga et al. | Nov 2003 | B2 |
6658279 | Swanson et al. | Dec 2003 | B2 |
6694173 | Bende et al. | Feb 2004 | B1 |
6701181 | Tang et al. | Mar 2004 | B2 |
6751490 | Esenaliev et al. | Jun 2004 | B2 |
6764450 | Yock | Jul 2004 | B2 |
6831781 | Tearney et al. | Dec 2004 | B2 |
6833540 | MacKenzie et al. | Dec 2004 | B2 |
6839496 | Mills et al. | Jan 2005 | B1 |
6846288 | Nagar et al. | Jan 2005 | B2 |
6877894 | Vona et al. | Apr 2005 | B2 |
6937886 | Zavislan | Aug 2005 | B2 |
6956650 | Boas et al. | Oct 2005 | B2 |
7072045 | Chen et al. | Jul 2006 | B2 |
7198778 | Achilefu et al. | Apr 2007 | B2 |
7231243 | Tearney et al. | Jun 2007 | B2 |
7245789 | Bates et al. | Jul 2007 | B2 |
7266407 | Li et al. | Sep 2007 | B2 |
7322972 | Viator et al. | Jan 2008 | B2 |
7357029 | Falk | Apr 2008 | B2 |
7382949 | Bauma et al. | Jun 2008 | B2 |
7917312 | Wang et al. | Mar 2011 | B2 |
8016419 | Zhang et al. | Sep 2011 | B2 |
8025406 | Zhang et al. | Sep 2011 | B2 |
8397573 | Kobayashi | Mar 2013 | B2 |
8416421 | Wang et al. | Apr 2013 | B2 |
8454512 | Wang | Jun 2013 | B2 |
8764666 | Chen et al. | Jul 2014 | B2 |
9351705 | Wang | May 2016 | B2 |
20010052979 | Treado et al. | Dec 2001 | A1 |
20020176092 | Deck | Nov 2002 | A1 |
20030097066 | Shelby et al. | May 2003 | A1 |
20030160957 | Oldham et al. | Aug 2003 | A1 |
20030160967 | Houston et al. | Aug 2003 | A1 |
20040039379 | Viator et al. | Feb 2004 | A1 |
20040082070 | Jones et al. | Apr 2004 | A1 |
20050015002 | Dixon et al. | Jan 2005 | A1 |
20050143664 | Chen et al. | Jun 2005 | A1 |
20050154313 | Desilets et al. | Jul 2005 | A1 |
20050217381 | Falk | Oct 2005 | A1 |
20060055936 | Yun et al. | Mar 2006 | A1 |
20060058614 | Tsujita | Mar 2006 | A1 |
20060122516 | Schmidt et al. | Jun 2006 | A1 |
20060181791 | Van Beek et al. | Aug 2006 | A1 |
20060184042 | Wang et al. | Aug 2006 | A1 |
20060235299 | Martinelli | Oct 2006 | A1 |
20060264717 | Pesach et al. | Nov 2006 | A1 |
20070088206 | Peyman et al. | Apr 2007 | A1 |
20070213590 | Squicciarini | Sep 2007 | A1 |
20070213618 | Li et al. | Sep 2007 | A1 |
20070282200 | Johnson et al. | Dec 2007 | A1 |
20070299341 | Wang et al. | Dec 2007 | A1 |
20080088838 | Raicu et al. | Apr 2008 | A1 |
20080173093 | Wang et al. | Jul 2008 | A1 |
20080177183 | Courtney | Jul 2008 | A1 |
20080230717 | Ashkenazi et al. | Sep 2008 | A1 |
20090024038 | Arnold | Jan 2009 | A1 |
20090088631 | Dietz et al. | Apr 2009 | A1 |
20090116518 | Patel et al. | May 2009 | A1 |
20090138215 | Wang et al. | May 2009 | A1 |
20100079768 | Wang et al. | Apr 2010 | A1 |
20100245766 | Zhang et al. | Sep 2010 | A1 |
20100245769 | Zhang et al. | Sep 2010 | A1 |
20100245770 | Zhang et al. | Sep 2010 | A1 |
20100249562 | Zhang et al. | Sep 2010 | A1 |
20100268042 | Wang et al. | Oct 2010 | A1 |
20100285518 | Viator et al. | Nov 2010 | A1 |
20100309466 | Lucassen et al. | Dec 2010 | A1 |
20110021924 | Sethuraman et al. | Jan 2011 | A1 |
20110071402 | Masumura | Mar 2011 | A1 |
20110098572 | Chen | Apr 2011 | A1 |
20110122416 | Yang et al. | May 2011 | A1 |
20110201914 | Wang et al. | Aug 2011 | A1 |
20110282181 | Wang et al. | Nov 2011 | A1 |
20110282192 | Axelrod et al. | Nov 2011 | A1 |
20120070817 | Wang et al. | Mar 2012 | A1 |
20120204648 | Wang et al. | Aug 2012 | A1 |
20120275262 | Song et al. | Nov 2012 | A1 |
20120307250 | Wang et al. | Dec 2012 | A1 |
20130199299 | Wang et al. | Aug 2013 | A1 |
20130245406 | Wang et al. | Sep 2013 | A1 |
20140009808 | Wang et al. | Jan 2014 | A1 |
20140142404 | Wang et al. | May 2014 | A1 |
Number | Date | Country |
---|---|---|
0012262 | Jun 1980 | EP |
1493380 | Jan 2005 | EP |
H05126725 | May 1993 | JP |
2000292416 | Oct 2000 | JP |
2009068977 | Apr 2009 | JP |
2010017426 | Jan 2010 | JP |
2006111929 | Oct 2006 | WO |
2007148239 | Dec 2007 | WO |
2008062354 | May 2008 | WO |
2008100386 | Aug 2008 | WO |
2009055705 | Apr 2009 | WO |
2010048258 | Apr 2010 | WO |
2010080991 | Jul 2010 | WO |
2011091360 | Jul 2011 | WO |
2011127428 | Oct 2011 | WO |
2013086293 | Jun 2013 | WO |
Entry |
---|
Zharov et al., “In vivo photoacoustic flow cytometry for monitor of circulating single cancer cells and contrast agents,” Optics Letters, 31(24): 3623-3625 (2006). |
Zou et al., “BOLD response to visual stimulation in survivors of childhood cancer,” NeuroImage, 24(1): 61-69 (2005). |
International Search Report and Written Opinion from Application Serial No. PCT/US2008/081167, dated Apr. 22, 2009 (7 pages). |
International Search Report and Written Opinion from Application Serial No. PCT/US2009/061435, dated Mar. 29, 2010 (10 pages). |
International Search Report and Written Opinion from Application Serial No. PCT/US2010/020488, dated Aug. 31, 2010 (11 pages). |
International Search Report and Written Opinion from Application Serial No. PCT/US2011/022253, dated Sep. 22, 2011 (8 pages). |
International Search Report and Written Opinion from Application Serial No. PCT/US2011/031823, dated Dec. 26, 2011 (8 pages). |
International Search Report and Written Opinion from Application Serial No. PCT/US2012/068403, dated Mar. 19, 2013 (10 pages). |
Extended European Search Report from European Application Serial No. 08842292.8, dated Dec. 17, 2013 (8 pages). |
Office Action from related U.S. Appl. No. 11/625,099, dated Nov. 1, 2010 (11 pages). |
Office Action from related U.S. Appl. No. 11/625,099, dated Apr. 20, 2010 (11 pages). |
Office Action from related U.S. Appl. No. 12/254,643, dated Aug. 6, 2010 (9 pages). |
Notice of Allowance from related U.S. Appl. No. 12/254,643, dated Nov. 22, 2010 (8 pages). |
Office Action from related U.S. Appl. No. 12/568,069, dated Dec. 21, 2012 (10 pages). |
Office Action from related U.S. Appl. No. 12/568,069, dated Mar. 29, 2012 (10 pages). |
Office Action from related U.S. Appl. No. 12/568,069, dated Sep. 18, 2012 (14 pages). |
Notice of Allowance from related U.S. Appl. No. 12/568,069, dated Feb. 22, 2013 (7 pages). |
Office Action from related U.S. Appl. No. 12/739,589, dated Jul. 19, 2012 (9 pages). |
Notice of Allowance from related U.S. Appl. No. 12/739,589, dated Feb. 5, 2013 (9 pages). |
Office Action from related U.S. Appl. No. 13/125,522, dated Jan. 22, 2013 (8 pages). |
Office Action from related U.S. Appl. No. 13/125,522, dated May 23, 2013 (10 pages). |
Office Action from related U.S. Appl. No. 13/125,522, dated Jul. 17, 2014 (10 pages). |
Office Action from related U.S. Appl. No. 13/369,558, dated Jun. 20, 2014 (10 pages). |
Notice of Allowance from related U.S. Appl. No. 13/369,558, dated Jul. 29, 2014 (7 pages). |
Office Action from related U.S. Appl. No. 13/450,793, dated Jun. 5, 2013 (20 pages). |
Office Action from related U.S. Appl. No. 13/450,793, dated Nov. 22, 2013 (22 pages). |
Office Action from related U.S. Appl. No. 13/450,793, dated Mar. 24, 2014 (22 pages). |
Office Action from related U.S. Appl. No. 13/450,793, dated Aug. 1, 2014 (21 pages). |
Office Action from related U.S. Appl. No. 13/574,994, dated Mar. 17, 2014 (9 pages). |
Office Action from related U.S. Appl. No. 13/574,994, dated Aug. 26, 2014 (10 pages). |
Office Action from related U.S. Appl. No. 13/637,897, dated Aug. 1, 2014 (7 pages). |
Nakajima et al., “Three-dimensional analysis and classification of arteries in the skin and subcutaneous adipofascial tissue by computer graphics imaging,” Plastic and Reconstructive Surgery, 102(3): 748-760 (1998). |
Nelson et al., “Imaging gliblastoma multiforme,” Cancer Journal, 9(2): 134-145 (2003). |
Niederhauser et al., “Combined Ultrasound and Optoacoustic System for Real-Time High-Contrast Vascular Imaging in Vivo,” IEEE Transactions on Medical Imaging, 24(4): 436-440 (2005). |
Oraevsky et al., “Laser Optoacoustic Tomography of Layered Tissues: Signal Processing,” Proceedings of SPIE, 2979: 59-70 (1997). |
Oraevsky et al., “Ultimate Sensitivity of Time-Resolved Opto-Acoustic Detection,” In Biomedical Optoacoustics, Proceedings of SPIE, 3916: 228-239 (2000). |
Oraevsky et al., “Optoacoustic Tomography,” Biomedical Photonics Handbook, CRC Press LLC, USA, pp. 1-40 (2003). |
Oraevsky et al., “Laser opto-acoustic imaging of the breast: detection of cancer angiogenesis,” Proceedings of SPIE, 3597: 352-363 (1999). |
Petrov et al., “Optoacoustic, Noninvasive, Real-Time, Continuous Monitoring of Cerebral Blood Oxygenation: An In Vivo Study in Sheep,” Anesthesiology, 102(1): 69-75 (2005). |
Potter et al., “Capillary diameter and geometry in cardiac and skeletal muscle studied by means of corrosion casts,” Microvascular Research, 25(1): 68-84 (1983). |
Robert et al., “Fabrication of focused poly (vinylidene fluoride-trifluoroethylene) P (VDF-TrFE) copolymer 40-50 MHz ultrasound transducers on curved surfaces,” Journal of Applied Physics, 96(1): 252-256 (2004). |
Saager et al., “Direct characterization and removal of interfering absorption trends in two-layer turbid media,” Journal of the Optical Society of America A, 22(9): 1874-1882 (2005). |
Savateeva et al., “Noninvasive detection and staging of oral cancer in vivo with confocal optoacoustic tomography,” Proceedings of SPIE, 3916: 55-66 (2000). |
Schmidt et al., “A 32-channel time-resolved instrument for medical optical tomography,” Review of Scientific Instruments, 71(1): 256-265 (2000). |
Schroeter et al., “Spontaneous slow hemodynamic oscillations are impaired in cerebral microangiopathy,” Journal of Cerebral Blood Flow & Metabolism, 25(12): 1675-1684 (2005). |
Sethuraman et al., “Development of a combined intravascular ultrasound and photoacoustic imaging system,” Proceedings of SPIE, 6086: 60860F.1-60860F.10 (2006). |
Sethuraman et al., “Intravascular photoacoustic imaging of atherosclerotic plaques: ex vivo study using a rabbit model of atherosclerosis,” Proceedings of SPIE, 6437: 643729.1-643729.9 (2007). |
Sheth et al., “Columnar Specificity of Microvascular Oxygenation and Volume Responses: Implications for Functional Brain Mapping,” Journal of Neuroscience, 24(3): 634-641 (2004). |
Shmueli et al., “Low-frequency fluctuations in the cardiac rate as a source of variance in the resting-state fMRI BOLD signal,” NeuroImage, 38(2): 306-320 (2007). |
Siphanto et al., “Imaging of Small Vessels Using Photoacoustics: An In Vivo Study,” Lasers in Surgery and Medicine, 35(5): 354-362 (2004). |
Song et al., “Fast 3-D dark-field reflection-mode photoacoustic microscopy in vivo with a 30-MHz ultrasound linear array,” Journal of Biomedical Optics, 13(5): 054028.1-054028.5 (2008). |
Song et al., “Section-illumination photoacoustic microscopy for dynamic 3D imaging of microcirculation in vivo,” Optics Letters, 35(9): 1482-1484 (2010). |
Steinbrink et al., “Illuminating the BOLD signal: combined fMRI-fNIRS studies,” Magnetic Resonance Imaging, 24(4): 495-505 (2006). |
Stern, MD., “In vivo evaluation of microcirculation by coherent light scattering,” Nature, 254(5495): 56-58 (1975). |
Tam, A.C., “Applications of photoacoustic sensing techniques,” Reviews of Modern Physics, 58(2): 381-431 and Figs. 16, 26 and 32 (1986). |
Tearney et al., “Scanning single-mode fiber optic catheter-endoscope for optical coherence tomography,” Optics Letters, 21(7): 543-545 (1996). |
Tran et al., “In vivo endoscopic optical coherence tomography by use of a rotational microelectromechanical system probe,” Optics Letters, 29(11): 1236-1238 (2004). |
Van Essen et al., “An Integrated Software Suite for Surface-based Analyses of Cerebral Cortex,” Journal of the American Medical Informatics Association, 8(5): 443-459 (2001). |
Viator et al., “Design and testing of an endoscopic photoacoustic probe for determination of treatment depth after photodynamic therapy,” Proceedings of SPIE in Biomedical Optoacoustics II, 4256: 16-27 (2001). |
Wang et al., “Ballistic 2-D Imaging Through Scattering Walls Using an Ultrafast Optical Kerr Gate,” Science, 253(5021):769-771 (1991). |
Wang et al., “MCML—Monte Carlo modeling of light transport in multi-layered tissues,” Computer Methods and Programs in Biomedicine, 47(2): 131-146 (1995). |
Wang et al., “Noninvasive laser-induced photoacoustic tomography for structural and functional in vivo imaging of the brain,” Nature Biotechnology, 21(7): 803-806 (2003). |
Wang et al., “Three-dimensional laser-induced photoacoustic tomography of mouse brain with the skin and skull intact,” Optics Letters, 28(19): 1739-1741 (2003). |
Wang et al., “Noninvasive photoacoustic angiography of animal brains in vivo with near-infrared light and an optical contrast agent,” Optics Letters, 29(7): 730-732 (2004). |
Wang et al., “Biomedical Optics, Principles and Imaging,” 2007, Wiley-Interscience, A John Wiley & Sons, Inc., Hoboken, New Jersey, US (7 pages). |
Wang, L. V., “Multiscale photoacoustic microscopy and computed tomography,” Nature Photonics, 3(9): 503-509 (2009). |
Wang et al., “Intravascular Photoacoustic Imaging”, IEEE J Quantum Electronics, 16(3): 588-599 (2010). |
Xu et al., “Photoacoustic imaging in biomedicine,” Review of Scientific Instruments, 77(4): 041101.1-041101.22 (2006). |
Xu et al., “Time Reversal Ultrasound Modulated Optical Tomography Using a BSO Phase Conjugate Mirror,” poster presented at SPIE Conference 7177 on Jan. 26, 2009; 3 pgs. |
Yadlowsky et al., “Multiple scattering in optical coherence microscopy,” Applied Optics, 34(25): 1699-5707 (1995). |
Yang et al., “Optical coherence and Doppler tomography for monitoring tissue changes induced by laser thermal therapy—An in vivo feasibility study,” Review of Scientific Instruments, 74(1): 437-440 (2003). |
Yang et al., “Novel biomedical imaging that combines intravascular ultrasound (IVUS) and optical coherence tomography (OCT),” IEEE International Ultrasonics Symposium, Beijing, China, Nov. 2-5, 2008, pp. 1769-1772. |
Yao et al., “Monte Carlo simulation of an optical coherence tomography signal in homogeneous turbid media,” Physics in Medicine & Biology, 44(9): 2307-2320 (1999). |
Yaqoob et al., “Methods and application areas of endoscopic optical coherence tomography,” Journal of Biomedical Optics, 11(6): 063001.1-063001.19 (2006). |
Yodh et al., “Spectroscopy and Imaging With Diffusing Light,” Physics Today, 48(3): 34-40 (1995). |
Yodh et al., “Functional Imaging with Diffusing Light,” Biomedical Photonics Handbook, 2003, Chapter 21, CRC Press, Boca Raton (45 pgs). |
Zeff et al., “Retinotopic mapping of adult human visual cortex with high-density diffuse optical tomography,” Proceedings of the National Academy of Sciences, 104(29): 12169-12174 (2007). |
Zemp et al., “Realtime photoacoustic microscopy in vivo with a 30-MHz ultrasonic array transducer,” Optics Express, 16(11): 7915-7928 (2008). |
Zhang et al., “Intrinsic Functional Relations Between Human Cerebral Cortex and Thalamus,” J Neurophysiology, 100(4): 1740-1748 (2008). |
Zhang et al., “Functional photoacoustic microscopy for high-resolution and noninvasive in vivo imaging,” Nature Biotechnology, 24(7): 848-851 (2006). |
Zhang et al., “In vivo imaging of subcutaneous structures using functional photoacoustic microscopy,” Nature Protocols, 2(4): 797-804 (2007). |
Ai et al., “Spectral-domain optical coherence tomography: Removal of autocorrelation using an optical switch,” Applied Physics Letters, 88(11): 111115-1 to 111115-3 (2006). |
Allen et al., “Pulsed near-infrared laser diode excitation system for biomedical photoacoustic imaging,” Optics Letters, 31(23): 3462-3464 (2006). |
Bell, Alexander Graham “On the Production and Reproduction of Sound by Light,” American Journal of Sciences, Third Series, 20(118): 305-324 (1880). |
Calasso et al., “Photoacoustic Point Source,” Physical Review Letters, 86(16): 3550-3553 (2001). |
Cannata et al., “Development of a 35-MHz Piezo-Composite Ultrasound Array for Medical Imaging,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 53(1): 224-236 (2006). |
Cheong et al., “A review of the optical properties of biological tissues,” IEEE J. Quantum Electronics, 26(12): 2166-2185 (1990). |
D'Andrea et al., “Time-resolved optical imaging through turbid media using a fast data acquisition system based on a gated CCD camera,” Journal of Physics D: Applied Physics, 36(14): 1675-1681 (2003). |
De Boer et al., “Improved signal-to-noise ratio in spectral-domain compared with time-domain optical coherence tomography,” Optics Letters, 28(21): 2067-2069 (2003). |
Diebold et al., “Photoacoustic “Signatures” of Particulate Matter: Optical Production of Acoustic Monopole Radiation,” Science, 250(4977): 101-104 (1990). |
Diebold et al., “Photoacoustic Monopole Radiation in One, Two, and Three Dimensions,” Physical Review Letters, 67(24): 3384-3387 and Figs. 1 and 2 (1991). |
Dunn et al., “Transport-based image reconstruction in turbid media with small source-detector separations,” Optics Letters, 25(24): 1777-1779 (2000). |
Ermilov et al., “Laser optoacoustic imaging system for detection of breast cancer,” Journal of Biomedical Optics, 14(2): 024007-024007-14 (2009). |
Erpelding et al., “Sentinel Lymph Nodes in the Rat: Noninvasive Photoacoustic and US Imaging with a Clinical US System,” Radiology, 256(1): 102-110 (2010). |
Fan et al., “Development of a laser photothermoacoustic frequency-swept system for subsurface imaging: Theory and experiment,” Journal of Acoustical Society of America, 116(6): 3523-3533 (2004). |
Fang et al., “Photoacoustic Doppler Effect from Flowing Small Light-Absorbing Particles,” Physical Review Letters, 99(18): 184501-184501-4 (2007). |
Fercher et al., “Measurement of intraocular distances by backscattering spectral interferometry,” Optics Communications, 117(1-2): 43-48 (1995). |
Foster et al., “Advances in Ultrasound Biomicroscopy,” Ultrasound in Medicine and Biology, 26(1): 1-27 (2000). |
Gibson et al., “Recent advances in diffuse optical imaging,” Physics in Medicine and Biology, 50(4): R1-R43, (2005). |
Guittet et al., “In vivo high-frequency ultrasonic characterization of human dermis,” IEEE Transactions on Biomedical Engineering, 46(6): 740-746 (1999). |
Hebden et al., “Enhanced time-resolved imaging with a diffusion model of photon transport,” Optics Letters, 19(5): 311-313 (1994). |
Hee et al., “Femtosecond transillumination tomography in thick tissues,” Optics Letters, 18(13): 1107-1109 (1993). |
Hillman et al., “Laminar optical tomography: demonstration of millimeter-scale depth-resolved imaging in turbid media,” Optics Letters, 29(14): 1650-1652 (2004). |
Hoelen et al., “Three-dimensional photoacoustic imaging of blood vessels in tissue,” Optics Letters, 23(8): 648-650 (1998). |
Hu et al., “Label-free photoacoustic ophthalmic angiography,” Optics Letters, 35(1): 1-3 (2010). |
Huang et al., “Optical Coherence Tomography,” Science, New Series, 254(5035): 1178-1181 (1991). |
Huber et al., “Three-dimensional and C-mode OCT imaging with a compact, frequency swept laser source at 1300 nm,” Optics Express, 13(26): 10523-10538 (2005). |
Karamata et al., “Multiple scattering in optical coherence tomography. I. Investigation and modeling,” Journal Optical Society of America, 22(7): 1369-1379 (2005). |
Kim et al., “In Vivo Molecular Photoacoustic Tomography of Melanomas Targeted by Bioconjugated Gold Nanocages,” ACS Nano, 4(8): 4559-4564 (2010). |
Kolkman et al., “In vivo photoacoustic imaging of blood vessels using an extreme-narrow aperture sensor,” IEEE Journal on Selected Topics in Quantum Electronics, 9(2): 343-346 (2003). |
Kruger et al., “Photoacoustic ultrasound (PAUS)—Reconstruction tomography,” Medical Physics, 22(10): 1605-1609 (1995). |
Kruger et al., “Thermoacoustic computed tomography—technical considerations,” Medical Physics, 26(9): 1832-1837 (1999). |
Kruger et al., “Breast Cancer in Vivo: Contrast Enhancement with Thermoacoustic CT at 434 MHz—Feasibility Study,” Radiology, 216(1): 279-283 (2000). |
Kruger et al., “Thermoacoustic computed tomography using a conventional linear transducer array,” Medical Physics, 30(5): 856-860 (2003). |
Kruger et al., “Thermoacoustic Molecular Imaging of Small Animals,” Molecular Imaging, 2(2): 113-123 (2003). |
Ku et al., “Scanning thermoacoustic tomography in biological tissue,” Medical Physics, 27(5): 1195-1202 (2000). |
Ku et al., “Scanning microwave-induced thermoacoustic tomography: Signal, resolution, and contrast,” Medical Physics, 28(1): 4-10 (2001). |
Ku et al., “Multiple-bandwidth photoacoustic tomography,” Physics in Medicine & Biology, 49(7): 1329-1338 (2004). |
Ku et al., “Deeply penetrating photoacoustic tomography in biological tissues enhanced with an optical contrast agent,” Optics Letters, 30(5): 507-509 (2005). |
Ku et al., “Imaging of tumor angiogenesis in rat brains in vivo by photoacoustic tomography,” Applied Optics, 44(5): 770-775 (2005). |
Ku et al., “Thermoacoustic and Photoacoustic Tomography of Thick Biological Tissues Toward Breast Imaging,” Technology in Cancer Research & Treatment, 4(5): 559-566 (2005). |
Leitgeb et al., “Performance of fourier domain vs. time domain optical coherence tomography,” Optics Express, 11(8): 889-894 (2003). |
Li et al., “Optical coherence computed tomography,” Applied Physics Letters, 91(14): 141107-141107-3 (2007). |
Li et al., “Simultaneous Molecular and Hypoxia Imaging of Brain Tumors In Vivo Using Spectroscopic Photoacoustic Tomography,” Proceedings of the IEEE, 96(3): 481-489 (2008). |
Manohar et al., “Initial Results of in vivo non-invasive cancer imaging in the human breast using near-infrared photoacoustics,” Optics Express, 15(19): 12277-12285 (2007). |
Maslov et al., “In vivo dark-field reflection-mode photoacoustic microscopy,” Optics Letters, 30(6): 625-627 (2005). |
Maslov et al., “Optical-resolution photoacoustic microscopy for in vivo imaging of single capillaries,” Optical Letters, 33(9): 929-931 (2008). |
Maslov et al., “Photoacoustic imaging of biological tissue with intensity-modulated continuous-wave laser,” Journal of Biomedical Optics, 13(2): 024006-024006-5 (2008). |
Mishra et al., “Development and comparison of the DTM, the DOM and the FVM formulations for the short-pulse laser transport through a participating medium,” International Journal of Heat & Mass Transfer, 49(11-12): 1820-1832 (2006). |
Morgner et al., “Spectroscopic optical coherence tomography,” Optics Letters, 25(2): 111-113 (2000). |
Murray et al., “High-sensitivity laser-based acoustic microscopy using a modulated excitation source,” Applied Physics Letters, 85(14): 2974-2976 (2004). |
Number | Date | Country | |
---|---|---|---|
20160235305 A1 | Aug 2016 | US |
Number | Date | Country | |
---|---|---|---|
61143668 | Jan 2009 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13143832 | US | |
Child | 15141189 | US |