WO2006131840A2 - Method and apparatus for ultrasound drug delivery and thermal therapy with phase-convertible fluids - Google Patents
Method and apparatus for ultrasound drug delivery and thermal therapy with phase-convertible fluids Download PDFInfo
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- WO2006131840A2 WO2006131840A2 PCT/IB2006/051673 IB2006051673W WO2006131840A2 WO 2006131840 A2 WO2006131840 A2 WO 2006131840A2 IB 2006051673 W IB2006051673 W IB 2006051673W WO 2006131840 A2 WO2006131840 A2 WO 2006131840A2
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M37/00—Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin
- A61M37/0092—Other apparatus for introducing media into the body; Percutany, i.e. introducing medicines into the body by diffusion through the skin using ultrasonic, sonic or infrasonic vibrations, e.g. phonophoresis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K41/00—Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
- A61K41/0028—Disruption, e.g. by heat or ultrasounds, sonophysical or sonochemical activation, e.g. thermosensitive or heat-sensitive liposomes, disruption of calculi with a medicinal preparation and ultrasounds
- A61K41/0033—Sonodynamic cancer therapy with sonochemically active agents or sonosensitizers, having their cytotoxic effects enhanced through application of ultrasounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/22—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations
- A61K49/222—Echographic preparations; Ultrasound imaging preparations ; Optoacoustic imaging preparations characterised by a special physical form, e.g. emulsions, liposomes
- A61K49/223—Microbubbles, hollow microspheres, free gas bubbles, gas microspheres
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/22—Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
- A61B17/22004—Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for using mechanical vibrations, e.g. ultrasonic shock waves
- A61B2017/22005—Effects, e.g. on tissue
- A61B2017/22007—Cavitation or pseudocavitation, i.e. creation of gas bubbles generating a secondary shock wave when collapsing
- A61B2017/22008—Cavitation or pseudocavitation, i.e. creation of gas bubbles generating a secondary shock wave when collapsing used or promoted
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B8/00—Diagnosis using ultrasonic, sonic or infrasonic waves
- A61B8/12—Diagnosis using ultrasonic, sonic or infrasonic waves in body cavities or body tracts, e.g. by using catheters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B8/00—Diagnosis using ultrasonic, sonic or infrasonic waves
- A61B8/54—Control of the diagnostic device
- A61B8/546—Control of the diagnostic device involving monitoring or regulation of device temperature
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
- A61N7/02—Localised ultrasound hyperthermia
Definitions
- the present embodiments relate generally to medical ultrasound systems and more particularly, to a method and apparatus for ultrasound drug delivery and thermal therapy with phase-convertible fluids.
- Microbubbles typically contain a gas encapsulated by a protein, lipid or biodegradable polymer layer or a combination thereof. They have a typical size in the range of a few micrometers.
- Another class of ultrasound contrast agents is formed by liquid perfluorocarbon filled particles. Liquid perfluorocarbon filled particles are much smaller in size than microbubbles and only visible in the ultrasound field when they are accumulated.
- microbubble agents With a trend towards targeting and drug delivery, microbubble agents have been modified to include drugs.
- the bubbles can be imaged and subsequently cavitated to locally release drugs, dna, or for instance, a contrast agent for another modality.
- a problem with the gas-filled bubbles of the microbubble agents is their limited lifetime in the circulation. Accumulation at the region of interest (ROI) can take hours, while today's microbubbles persist for minutes. The breakdown pathway of these microbubbles is not always clear, but it can be anticipated that it may lead to release of drugs slowly at undesired locations. Accordingly, there exists a need for a more stable ultrasound assisted drug delivery strategy.
- Yet another problem with microbubbles is that they remain in the vasculature and therefore drug delivery can only take place in or from the vasculature.
- Focused ultrasound (FUS) therapy has been investigated to thermally coagulate pathological tissue in the treatment of benign and cancerous tumors in several organs systems.
- focused ultrasound therapy can induce cavitation to mechanically destroy tissue
- the dominant opinion in the ultrasound therapy community has been to avoid cavitation and induce more predictable and controllable thermal damage with focused ultrasound.
- heating is used for treatment.
- thermal bioeffects are better characterized and controlled, yielding lesion sizes and shapes predicted by various models.
- FUS thermal ablation is performed with constant levels of ultrasound intensity, below the cavitation threshold, for durations of 1-30 seconds to raise the temperature at the focus to levels that denature protein.
- therapy in the thermal regime can be carefully monitored with thermometry techniques, most notably magnetic resonance imaging (MRI).
- MRI magnetic resonance imaging
- an ultrasound treatment includes applying ultrasound at a first energy level to a region of interest in a subject for activating a cavitation nucleation agent during a first portion of a treatment cycle.
- Ultrasound at a second energy level is applied to the region of interest during a second portion of the treatment cycle for implementing a desired thermal therapy in the presence of the cavitation nucleation agent activated during the first portion of the treatment cycle.
- the second energy level is at an energy level different from the first energy level.
- the method can be implemented by an ultrasound therapy treatment system, as well as in the form of a computer program product.
- Figure 1 is a partial block diagram view of an ultrasound therapy treatment system according to an embodiment of the present disclosure
- Figure 2 is a simplified schematic diagram view of therapeutic treatment of a target location with use of the ultrasound therapy treatment system according to an embodiment of the present disclosure
- Figure 3 is an exemplary timing diagram illustrating ultrasound therapy pressure versus time according to one embodiment of the present disclosure.
- Figure 4 contains pictoral views of (a) an MRI view showing a region of tissue with focus of a conventional therapeutic ultrasound heating exposure (no gas bubbles), (b) an MRI showing a region where heating is to occur, with bone just above a focal location, during gas-bubble enhanced heating according to an embodiment of the present disclosure, (c) an MRI temperature image showing heating as ultrasound reflects off the bone of the image of Figure 4(a) above the focal point, and (d) an MRI temperature image during a gas-bubble enhanced heating, post conversion of a corresponding phase-convertible agent, showing no heating above the focal point where the bone of Figure 4(b) might reflect energy, but does not, in view of the method according to the embodiments of the present disclosure.
- like reference numerals refer to like elements.
- the figures may not be drawn to scale.
- phase-convertible agents such as, perfluorocarbon-based solutions and emulsions can be safely injected into the blood stream. At normal body temperatures, these agents are in the liquid phase and can be synthesized with their boiling points lower than that of water.
- the method comprises using high intensity focused ultrasound to focally raise the acoustic pressure and/or temperature at a desired location.
- the method includes phase converting the phase-convertible agents to the gas phase and using the phase converted agents in the gas phase to enhance heating and heat- related biological effects.
- the phase-convertible agents could also be targeted to the sites of pathology, further localizing the focused ultrasound therapy.
- an ultrasound shielding effect of gas bubble layers could be used to protect critical anatomy during focused ultrasound therapy.
- heating-based focused ultrasound therapies in the presence of nanoparticles will ultimately reduce transducer power requirements, allow for the heating of larger areas, and better localize ultrasound energy deposition.
- the methods of therapeutic ultrasound with phase-convertible fluids overcome both the power disadvantages of inducing cavitation in tissue and the poor spatial control when heating in the presence of injected microbubble contrast agents.
- FIG. 1 is a block diagram view of an ultrasound therapy treatment system 10 according to an embodiment of the present disclosure.
- the ultrasound therapy treatment system 10 includes a control or base unit 12 configured for use with an ultrasound transducer probe 14, further for carrying out the ultrasound treatment methods as discussed herein according to the embodiments of the present disclosure.
- the probe 14 contains an ultrasound transducer 16.
- ultrasound transducer 16 comprises a high power ultrasound transducer.
- transducer 16 can comprise a single element or a phased array, wherein the choice between that of the single element or phased array is selected according to the requirements of a particular ultrasound treatment application.
- base unit 12 includes suitable control electronics for performing ultrasound therapy treatment as discussed herein.
- base unit 12 can comprise a computer as discussed further herein.
- Ultrasound transducer probe 14 couples to base unit 12 via a suitable connection, for example, an electronic cable, a wireless connection, or other suitable means.
- Figure 2 is a simplified schematic diagram view of ultrasound therapy treatment of a target location with use of the ultrasound treatment system 10 according to an embodiment of the present disclosure.
- ultrasound transducer 16 produces ultrasound energy 18 that is focused at a target location 20 in response to an activation signal from base unit 12.
- the focal point of the ultrasound energy can be adjusted as needed, for example by a repositioning of the probe 14 with respect to the target location 20 and/or through appropriate activation signals from base unit 12, according to the requirements of a particular ultrasound treatment application.
- Target location 20 is disposed in a region of interest within tissue 22 of a subject to be treated according to the methods of the present disclosure.
- tissue 22 may comprise any tissue within a human body or within an animal body.
- one or more contrast agents according to the embodiments of the present disclosure can be administered by injecting fluid using an intravenous (IV) or a site injection, as indicated by reference numeral 24.
- IV intravenous
- 24 site injection
- the intravenous can be administered distal from the region of interest, whereas, the injection can be administered proximate the region of interest.
- Figure 3 is an exemplary timing diagram illustrating ultrasound therapy pressure versus time according to one embodiment of the present disclosure.
- An initial high pressure, short duration phase conversion pulse 32 is used to focally create gas bubbles in response to phase-conversion of the nucleation cavitation agent.
- Pulse 34 comprises an immediately following heating exposure that makes use of the focally created gas bubbles to provide a gas-bubble enhanced heating exposure, the gas-bubble enhanced heating exposure providing a desired treatment to tissue 22 at the target location 20.
- the first pulse 32 corresponds to a first phase and the second pulse 34 corresponds to a second phase.
- pulse 32 occurs between times tl and t2 and pulse 34 occurs between times t2 and t3.
- Activation of the transducer 16 produces pulse 32, 34, and any other pulses, in response to appropriate activation signals from base unit 12.
- the transducer 16 could be activated with use of an intermittent pulsing scheme to allow for reperfusion.
- the intermittent pulsing scheme could include a first pulse for phase conversion, a second pulse for heating, an off period or period of no pulse to allow for new particles to flow into the treatment plane, and then repeating the intermittent pulsing scheme with the first pulse, the second pulse, and the off period of no pulse, for as many repetitions as may be desired for a given treatment plan.
- Figure 4 contains pictoral views of various images as discussed in the following.
- an MRI view shows a region of rabbit tissue with an X indicating the focus of a conventional therapeutic ultrasound heating exposure with no gas bubbles. Above and to the left of the focus in Figure 4(a) are bone structures, the bone structures appearing white.
- an MRI view shows a region where heating is to occur with bone just above a focal location, during gas-bubble enhanced heating according to an embodiment of the present disclosure.
- an MRI temperature image shows heating above the focal point as ultrasound reflects off the bone of the image of Figure 4(a).
- Figure 4(d) shows an MRI temperature image captured during a gas-bubble enhanced heating, post conversion of a corresponding phase-convertible agent.
- the image shows no heating above the focal point where the bone of Figure 4(b) might reflect energy, but does not, in view of the method according to the present embodiments.
- the gas-bubble is created by cavitation via a very high- pressure pulse, for example, pulse 32 of Figure 3.
- the method of gas-bubble enhanced ultrasound heating includes the use of biological safe, injectable phase- convertible fluids to gain the benefit of reducing therapeutic power requirements while maintaining tight spatial control of the ultrasound heating. Furthermore, the method provides benefits as outlined herein above.
- the method includes choosing a material configured to enhance the production of gas at the focus of a therapeutic ultrasonic transducer.
- the criteria for a correct choice of material involves the selection of a bulk material to be phase converted, a method of delivery (particle-like or homogeneous solution), characteristics of the delivery mechanism, and an appropriate concentration.
- An important aspect of the method, and corresponding design of such a system, is that the bulk material (or corresponding particles) be in a non-gaseous state at body temperature.
- the introduction of prescribed focused ultrasound energy instigates a phase change in the bulk material from solid/liquid to gas.
- the method further comprises use of perfluorocarbon-filled nanoparticles / microparticles that are in the liquid state at body temperature.
- the perfluorocarbon includes perfluorocarbon having a boiling point in a temperature range that is attainable through the introduction of focused ultrasound.
- the perfluorocarbon-filled nanoparticles / microparticles can comprise encapsulated particles or free droplets.
- the particular encapsulation is one selected to help control the onset of cavitation.
- common methods of encapsulation are through lipid layers and polymer shells.
- the choice of the size of the particles will depend on the application, with particles of appropriate size being chosen for their accessibility to a targeted vasculature, as well as to the size of the particles post-phase conversion.
- the embodiments of the present disclosure can also include the use of homogeneous solution as might occur, for example, in blood substitutes.
- One of the common methods of providing a blood substitute is to use a perfluorocarbon liquid.
- any or all of these agents may be coupled to an agent that binds to a specific target in the body.
- the agent may include an antibody to AlphaV-Beta3 integrin, which binds to areas of neo-vasculature as found in a tumor. By introducing an injection of the solution or fluid, one might also expect to cavitate or phase-convert this liquid with the use of focused ultrasound.
- the phased converted gas bubbles obtained via post conversion of a corresponding phase-convertible agent and provided by the various embodiments of the method of the present disclosure will have ultrasound- shielding effects. That is, the phase converted gas bubbles could also be used to protect tissues or vital anatomy beyond a gas layer during focused ultrasound therapy. Accordingly, the method further comprises creating shielding layers during therapy by phase-converting the fluid at the focus. In other words, the method includes ablating tissue at the ultrasound focus and protecting tissue beyond the ultrasound focus ( Figure 4).
- the phase-convertible liquid agent is injected intravascularly. Alternatively, the phase-convertible liquid agent can be injected in the vicinity of the treatment zone.
- FIG. 2 illustrates one example of a complete ultrasound exposure profile.
- phase-convertible liquid agent is injected intravascularly or in the vicinity of the treatment zone. After a period of time required for binding of the agent to the target location, focused ultrasound of sufficient energy is used to phase-convert the liquid into gas at the desired treatment location. Immediately following conversion, lower-pressure heating exposures focused at or below the phase- conversion focus are used to ablate or heat the treatment region in the presence of the phase-converted gas bubbles.
- Figure 3 illustrates one example of a complete ultrasound exposure profile.
- targeting is used to increase the amount of fixed phase-convertible agent at the desired treatment so that less power maybe required during both the phase-conversion and heating time periods.
- the initial phase conversion will be used to shield structures in a region beyond the therapeutic focus.
- the phase-convertible liquid agent is injected intravascularly or in the vicinity of the treatment zone. Focused ultrasound of sufficient energy is used to phase-convert the liquid into gas at the desired shielding location or locations.
- the phase-convertible liquid is selected so as to provide gas that can remain in the gas phase for a desired time duration at the shielding location or locations, subsequent to conversion of the liquid into gas. Then, focused ultrasound of sufficient energy is used to phase-convert the liquid into gas at the desired treatment location.
- the phase-convertible liquid is also selected so as to provide gas that can remain in the gas phase for a desired time duration at the treatment location, subsequent to conversion of the liquid into gas.
- shielding may be applied at a prescribed distance from the treatment zone.
- shielding proximate the treatment location provides protection of distal regions from heating effects originating at the treatment location. Such heating effects originating at the treatment location may be undesirable at the distal region or regions.
- the protected distal region corresponds to a region located on an opposite side of the shielding locations away from the treatment location.
- the embodiments described herein can be used in any application in which focused ultrasound is used to thermally ablate tissue.
- the embodiments can also be used in any applications where low temperature heating is desired for a bioeffect.
- the applications may include, but are not limited to, FDA approved HIFU devices for ablation of abdominal tumors, thermally activated gene therapy, thermally induced drug delivery, HIFU devices approved in Europe for prostate cancer, and future applications for treating brain tumors.
- FDA approved HIFU devices for ablation of abdominal tumors thermally activated gene therapy
- thermally induced drug delivery thermally induced drug delivery
- HIFU devices approved in Europe for prostate cancer and future applications for treating brain tumors.
- the method according to the embodiments of the present disclosure would reduce transducer and driving system power requirements and complexity such that ultrasound-heating therapy might be possible with unfocused transducers similar to conventional imaging transducers geometries.
- intracavitary application can be improved as transducer size-related power limitations may be overcome.
- focused ultrasound can be used to deposit energy at a region of interest.
- phase conversion of a liquid into a gas can be established at the ROI.
- the liquid such as a fluorinated liquid with a relatively low boiling point, but a boiling point above 37°C
- a shell such as a shell of a biodegradable polymer
- the shell will break up, gas escapes, and drug delivery or effective thermal treatment can take place.
- bubbles that have a gaseous core at body temperature these particles have a much better lifetime in the circulation.
- phase shift "emulsions" the liquids used in the embodiments of the present disclosure have the advantage that they will become liquid again after cooling down to body temperature, avoiding the formation of large gas bubbles in the circulation.
- phase conversion For local drug delivery, it is desirable to have an agent that has a phase conversion above body temperature and below the boiling point of water. Perfluorocarbons have, compared to corresponding alkanes, relatively low boiling points.
- perfluoro- octane has a boiling point of 99°C and per-fluoro heptane has a boiling point of 80°C. If the heat of evaporation is low compared to that of water, cavitation can be achieved using ultrasound, especially with therapeutic ultrasound transducers. Having a boiling point above body temperature also leads to condensation once the ultrasound is stopped and the temperature in the ROI decreases again. As a result, the risk of formation of uncontrollable large gas bubbles is therefore minimized.
- Imaging Perfluorocarbon containing nanoparticles have been imaged by Wickline, when accumulated on fibrin. Contrary to microbubbles, perfluorocarbon containing nanoparticles could not be detected when flowing in the vasculature.
- the method includes using bigger particles, thereby making imaging easier.
- the perfluorocarbon containing nanoparticles can be imaged using Fluor MRI.
- thermal therapy Upon phase conversion, gas bubbles appear that give a high acoustic signal and that can be imaged using suitable measuring techniques, for instance detecting harmonics or using phase inversion.
- phase-converted gas bubbles increases dramatically the local tissue absorption at the site of the gas bubbles. Accordingly, the first pulse of the therapy beam is used to phase convert, then CW (continuous wave) ultrasound is used to heat at the desired treatment area. From studies, it has been shown that up to three (3) times larger lesions for equivalent ultrasound power when microbubbles are present can be achieved at the thermal focus. Accordingly, ultrasound power can be dropped and similar lesion size obtained when phase-converted microbubbles from the phase-convertible liquid are present. Another significant advantage of phase-converted microbubbles from the phase-convertible liquid at the focus region when thermal heating is intiated is that temperature rise occurs much faster.
- Liquid perfluorocarbon containing particles can be prepared using emulsion methods.
- the shell forming material for instance biodegradable polymers such as polylactic acid, poly glycolic acid, polycaprolacton mixtures or copolymers thereof are dissolved in a suitable solvent.
- the perfluorocarbon is added and mixed well into the polymer solution.
- an emulsion in water is made by pouring the fluorocarbon containing polymer solution in an aqueous solution.
- the aqueous solution may contain a stabilizer, an often used stabilizer is poly vinyl alcohol.
- the emulsion can be processed to obtain the desired size distribution by standard emulsification and filtration methods.
- a stabilizer added to the aqueous phase a block copolymer having a hydrophilic block can be used as one of the polymers employed to make the shell of the particles.
- a common choice for this hydrophilic block is poly ethylene oxide, which has the advantage that it delays the uptake of the particle by the RES.
- a pegylated chain can be used as a starting point for the synthesis of a targeted agent.
- drop-by-drop emulsification methods such those using cross-flow filtration, liquid jets are preferred.
- the solvent for the polymer has to be removed. Often a solvent is chosen that has a fairly low boiling point or a reasonable solubility is the aqueous phase. As a consequence, the emulsion droplets will shrink. As the polymer will become insoluble upon removal of the solvent, it will form a shell and the remaining liquid will form the core of the particle.
- Lipophilic drugs can be incorporated using the emulsification procedure described above.
- a solution of the drug in oil with a very high boiling point (the oil should not be cavitated) can be added to the polymer solution. At sufficiently low initial concentrations, this does not affect the solubility of the polymer.
- An example of a drug that can be incorporated using this route is paclitaxel.
- Hydrophilic drugs or dna require a different preparation procedure.
- double emulsion techniques have to be used.
- a small amount water containing the drug or the dna is emulsified with the polymer solution and the perfluororcarbon.
- This first emulsion is subsequently poured into an aqueous phase not containing the drug, as is known for a double emulsion preparation of a cavitation nucleation agent.
- An interesting hydrophilic drug is adenosine that is used in making stress echo's. Examples:
- the embodiments of the present disclosure also include computer software or a computer program product.
- the computer program product includes a computer readable media having a set of instructions for carrying out the method of the ultrasound treatment as described and discussed herein.
- the computer readable media can include any suitable computer readable media for a given ultrasound diagnostic/therapeutic imaging system application.
- the computer readable media may include a network communication media. Examples of network communication media include, for example, an intranet, the Internet, or an extranet.
- the embodiments of the present disclosure can also be applied to any phase-convertible nucleation cavitation agent having a boiling point above 100 degrees C. Such an instance might be useful if the system locally lowers the pressure with ultrasound thereby affecting the corresponding agent's published boiling point. Furthermore, locally in a focused region of interest, the system can heat the region of interest to above 100 degrees C for the phase conversion. Furthermore, embodiments of the present disclosure may also be used in non- intra- venous manners, for example, via intra-mascular or even intracavity (such as, in the uterus) where larger particles for the phase-convertible neucleation cavitation agents can be used. In such an instance, the particle size can be greater than 10 microns.
- any reference signs placed in parentheses in one or more claims shall not be construed as limiting the claims.
- the word “comprising” and “comprises,” and the like, does not exclude the presence of elements or steps other than those listed in any claim or the specification as a whole.
- the singular reference of an element does not exclude the plural references of such elements and vice- versa.
- One or more of the embodiments may be implemented by means of hardware comprising several distinct elements, and/or by means of a suitably programmed computer. In a device claim enumerating several means, several of these means may be embodied by one and the same item of hardware.
- the mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to an advantage.
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EP06765709A EP1904179A2 (en) | 2005-06-07 | 2006-05-25 | Method and apparatus for ultrasound drug delivery and thermal therapy with phase-convertible fluids |
JP2008515330A JP5340728B2 (en) | 2005-06-07 | 2006-05-25 | Method and apparatus for ultrasonic drug delivery and thermal treatment with phase variable fluid |
US11/914,777 US8932239B2 (en) | 2005-06-07 | 2006-05-25 | Method and apparatus for ultrasound drug delivery and thermal therapy with phase-convertible fluids |
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US68800805P | 2005-06-07 | 2005-06-07 | |
US60/688,008 | 2005-06-07 |
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US (1) | US8932239B2 (en) |
EP (1) | EP1904179A2 (en) |
JP (1) | JP5340728B2 (en) |
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JP5340728B2 (en) | 2013-11-13 |
CN101291705A (en) | 2008-10-22 |
EP1904179A2 (en) | 2008-04-02 |
JP2008541975A (en) | 2008-11-27 |
US8932239B2 (en) | 2015-01-13 |
US20080200845A1 (en) | 2008-08-21 |
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