Provided is a method for treating metastatic disease or any other tumor that cannot easily or readily localized or localized at all using immersion mechanotherapy. The method includes providing a vessel containing an amount of medium for immersing at least a portion of a subject, and applying one or more programmed cycles of ultrasound waves to the subject through the medium for a pre-determined period of time. Also provided is a device for implementing the immersion mechanotherapy.

A method of changing the volume of an intra-bilayer membrane space of at least one bilayer membranous structure of a target tissue. The method comprises providing at least one characteristic of a target tissue having at least one bilayer membranous structure, selecting an acoustic energy transmission pattern set to change a volume of an intra-bilayer membrane space of a bilayer membrane of the at least one bilayer membranous structure according to the at least one characteristic, and applying acoustic energy on the target tissue according to the selected acoustic energy transmission pattern.

Various approaches for focusing an ultrasound transducer include introducing at least one transient acoustic reflector located in proximity to at least one target region; generating multiple sonications to the at least one target region; measuring a reflection signal of each of the sonications off the at least one transient acoustic reflector; selecting the measured reflection signals, and based at least in part on the selected reflection signals, adjusting a parameter value associated with at least one of the transducer elements so as to improve an ultrasound focus at the target region.

Provided are products of manufacture and methods for the removal and/or destruction of a biofilm in situ, e.g., a gastro-luminal biofilm, and for the treatment or amelioration of biofilm-associated diseases, infections and conditions, including and GI luminal infections. Provided are devices and apparatus, and methods for using them, for the removal, disruption and/or destruction of a biofilm in situ, e.g., a gastro-luminal biofilm. In alternative embodiments, provided are devices and apparatus, and methods, for enhancing biofilm dissolving or disrupting agents, or for administering biofilm dissolving or disrupting agents, where in alternative embodiments the biofilm comprises a gastro-luminal ‘unstirred layer’, adherent layer or gastro-luminal mucus layer; or the biofilm comprises a matrix or a DNA-containing layer, or alternatively the biofilm comprises a polysaccharide gastro-luminal peripheral layer.

An improved method for MRI-guided sonosensitized focused ultrasound treatment of malignant tissue is disclosed herein.

A method for performing spectral analysis and determining a safety marker includes an assembly via which: regularly, during shot Bb, at a series of times ta, the variation as a function of time in the spectral lines corresponding to the subharmonic and ultra-harmonic frequencies of a received acoustic-response signal of the microbubbles is measured, and the variation as a function of time, over the times ta, in a safety marker is determined and quantified, the safety marker being defined, at each time ta, by a number MDDa equal to the ratio of the sum of the areas of the spectral lines, measured at the time ta and corresponding to the subharmonic and/or ultra-harmonic frequencies of the received acoustic-response signal of the microbubbles, to the sum of the areas of the spectral lines, measured at the first time t1 and corresponding to the subharmonic and/or ultra-harmonic frequencies of the acoustic-response signal of the microbubbles. A system for performing spectral analysis and determining a safety marker implements said method.

A method is provided for achieving transfection of host cells using sonoporation. An acoustic radiation generator is positioned in acoustic coupling relationship with respect to a reservoir containing host cells to be transfected, exogenous material to be incorporated into the host cells, and a cell-compatible fluid medium. The acoustic radiation generator is activated to generate acoustic radiation and direct the acoustic radiation into the reservoir in a manner effective to enable transfection of the host cells with the exogenous material.

Transcutaneous, ultrasound-mediated methods for administering compound(s) to subject tissue(s) are provided. Examples involve positioning an occluding device in a vessel such that the blockage is adjacent to target tissue; engaging the device to occlude outflow from a region adjacent to the tissue; administering compound(s) to the vessel such that it is substantially retained adjacent to the target tissue; determining the location of the compound and/or a detectable adjunct compound optionally administered with the compound, using diagnostic ultrasound, radiography, or fluorography; administering therapeutic ultrasound energy transcutaneously to mediate delivery of the compound across the vessel wall and into adjacent target tissue.

Methods and systems are provided for treating target cells in a target tissue. The method comprises: determining frequency and magnitude of a periodic force to be applied to the target cells to trigger a mechanically-induced apoptotic process in the target cells; and generating a sequence of programmed cycles of waves to the target tissue to apply the periodic forces to the target cells for a period of time. In some cases, the frequency, magnitude and the period of time are determined based at least in part on the type of target cells or mechanical properties of the target cells.

The present invention is directed to methods for treating neurodegenerative diseases and/or improving cognitive function, in particular those associated with protein oligomers, aggregates or deposits, using acoustic energy, such as ultrasound. An 5 example of such a neurodegenerative disease is Alzheimer's disease. The present invention provides a method of improving cognitive function and/or memory in an individual with impaired memory and/or executive function, the method including the steps of identifying a region of the brain of the individual to be treated with acoustic energy, applying a clinically safe level of acoustic energy to the region, thereby 10 saturating or substantially saturating the region with acoustic energy, thereby improving memory in the individual.