The present disclosure provides imaging agents that are useful for the detection and evaluation of heart conditions, such as myocardial infarction. Upon activation, the imaging agents of the present disclosure may be detected using an ultrasound imaging device.

A coupling agent composition is provided and includes a plurality of non-toxic components in an amount equal to or greater than 97 weight percent (wt %). The coupling agent composition includes a carrier of water, at least one water soluble polyol selected from the group consisting of propanediol, pentylene glycol, and butylene glycol in an amount of from about 1.0 to about 20.0 wt %, a thickening agent in an amount of about 0.05 to about 5.00 wt %, and a balance of incidental impurities.

Disclosed are articles, devices and systems providing a semi-rigid acoustic coupling medium for ultrasound diagnostic and treatment techniques. In some aspects, an acoustic coupling article includes a semi-rigid acoustic coupling medium (SACM) able to conform to a receiving body through deformation of the SACM body in order to propagate an acoustic signal within the SACM to and from the receiving body. In some embodiments, the SACM is configured in a shape having one or more attachment portions located at one end of an acoustic interface portion, such that the acoustic interface portion is operable to contact the receiving body to propagate the acoustic signal and the attachment portions are configured to be secured by an acoustic probe device to transmit and receive the propagated acoustic signal.

Acoustically activatable particles having low vaporization energy are disclosed. A particle of material includes a first substance that includes at least one component that has a boiling point below 25° C. at atmospheric pressure. A second substance, different from the first substance, encapsulates the first substance to create the particle. The particle has a core consisting of a liquid and is an activatable phase change agent. The second substance includes a polymeric brush layer to prevent aggregation and coalescence.

Provided herein are improved methods for preparing phospholipid formulations including phospholipid UCA formulations.

A hydrogel marker is placed under stress during its curing stage, in one embodiment, by application of an externally applied force. The stress may also be induced during or after the dehydration process. The direction of the externally applied force increases the length, width, depth, or radial extent of the marker. The elastic limit of the marker is exceeded when the external force is applied so that the marker substantially retains its stressed size and shape when the externally applied force is removed. When the stretched or otherwise deformed dehydrated marker is hydrated, it substantially returns to the configuration it had prior to its dehydration and prior to the application of the externally applied force.

The present disclosure provides imaging agents that are useful for the detection and evaluation of heart conditions, such as myocardial infarction. Upon activation, the imaging agents of the present disclosure may be detected using an ultrasound imaging device.

A thermo-responsive ultrasound coupling gel that contains a thermo-responsive polymer such as poly(n-isopropyl acrylamide), the gel having a phase shift at a temperature in the range of 32 to 35° C. such that the gel has a loss factor G″/G′ of >1 at <32° C. and a loss factor G″/G′ of <1 at >35° C. The gel can also contain at least one of a solvent and gelling agent. Methods and uses for the thermo-responsive ultrasound coupling gel in an ultrasound and/or ultrasound guided procedure.

A method of generating bubbles of a first fluid in a second fluid, the method comprising: flowing a stream of the second fluid through a microfluidic channel; injecting a stream of the first fluid into the microfluidic channel through an aperture such that bubbles of the first fluid form in the second fluid; and sonicating the microfluidic channel with ultrasound so as to cause the bubbles formed at the aperture to divide.

Couplers for ultrasound probes can have a solid coupler body and a probe attachment member that is secured to a coupler body. The probe attachment member may extend upwardly from the coupler body. The probe attachment member may frictionally and/or adhesively engage with an ultrasound probe, thereby attaching and/or holding the coupler body to an end of the ultrasound probe. The coupler body may include at least one open channel that that extends through the coupler body to define a fluid path. The at least one open channel may be sized to hold and/or contain a fluid and/or gel in and/or on the coupler body and only release the fluid and/or gel when a force is exerted at a top surface of the coupler body. A coupler may be provided in a package in an orientation and easy to use fashion that may aid in attaching the coupler to an end of an ultrasound probe.