Ultrasound Microbubble Binding Dynamics Analysis

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Solution Overview

Problem

Current ultrasound-based targeted molecular imaging techniques face challenges in distinguishing specific from non-specific microbubble binding in blood vessel environments, requiring control groups and lengthy procedures due to the inability to differentiate between desirable and undesirable binding signals, which limits detection specificity and increases procedure time.

Innovation Solution

A system and method that analyze microbubble binding dynamics under modulated acoustic radiation force (ARF) to differentiate specific from non-specific binding, using a model for microbubble response to a modulated ARF pulse sequence and extracting parameters from echo data to determine the ratio of residual to saturated signal magnitude, allowing for real-time detection independent of control populations.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If control groups are used to estimate non-specific adhesion background, then measurement precision of specific binding is improved, but device complexity and procedure time increase due to requiring multiple microbubble populations and extended imaging periods

Engineering Contradiction:
Improvespecific binding detection accuracyVSAvoidprocedure complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent extracts and eliminates the control group requirement by using acoustic radiation force to selectively remove non-specifically bound microbubbles from the imaging region. This allows specific binding detection without requiring separate control populations, directly resolving the contradiction between measurement precision and procedure complexity

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

Acoustic radiation force serves as an intermediary mechanism that differentiates specific from non-specific binding. By applying controlled acoustic forces, the system selectively detaches non-specifically bound microbubbles while leaving specifically bound microbubbles attached, enabling direct measurement of specific binding without control groups

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If control groups are used to differentiate specific from non-specific binding, then measurement precision is improved, but loss of time increases due to requiring 20-30 minutes for microbubble clearance between injections

Engineering Contradiction:
Improvebinding specificity detectionVSAvoidprocedure time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent enables continuous imaging and measurement by using acoustic radiation force to clear non-specific microbubbles in place, eliminating the need to stop imaging for microbubble clearance periods. This maintains continuous useful action throughout the procedure, resolving the time loss contradiction

Inventive Principle:
Principle #20Continuity of useful action

Solution Approach 2:

The acoustic radiation force rapidly clears non-specific microbubbles in seconds rather than requiring 20-30 minute clearance periods. This rushes through the clearance step that previously caused significant time loss, while maintaining measurement precision

Inventive Principle:
Principle #21Skipping (Rushing through)

3Productivity

If acoustic radiation force is applied to increase binding efficacy, then productivity of targeted delivery is improved, but object-generated harmful factors increase due to non-specific molecular binding that creates false positive signals

Engineering Contradiction:
Improvetargeted delivery efficacyVSAvoidnon-specific binding signal
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The patent applies dynamic, modulated acoustic radiation force that can be adjusted in real-time. By controlling the timing and intensity of acoustic pulses, the system enhances specific binding while selectively removing non-specifically bound microbubbles, converting a static binding problem into a dynamic controllable process

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The patent converts the harmful effect of non-specific binding into a beneficial diagnostic tool. By applying acoustic radiation force, non-specifically bound microbubbles are selectively detached and identified as background signal, while specifically bound microbubbles remain attached. This transforms the previously harmful false positive signal into a measurable parameter that confirms specific binding

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables enhanced detection of targeted microbubble adhesion in real-time, reducing procedure time and improving specificity by accurately distinguishing specific from non-specific binding without the need for control groups, thereby improving the accuracy of targeted molecular imaging.

Implementation Method 1

acoustic radiation force (ARF) can be applied

Methodology Applied
Scientific EffectAcoustic radiation force: Acoustic Radiation Pressure

Implementation Method 2

echo data reflected from a region of interest

Methodology Applied
Scientific EffectEcho: Echo

Data Source

PatentUS9949722B2System and method for binding dynamics of targeted microbubbles
Publication Date: 2018.04.24 UNIV OF VIRGINIA PATENT FOUND
  • US9949722B2 patent drawing
  • US9949722B2 patent drawing
  • US9949722B2 patent drawing

AI summary

An ultrasound system and method that can include: a receive beamformer configured to receive signals from a transducer; a processor coupled to the receive beamformer, the processor configured to: analyze echo data reflected from a region of interest, the echo data elicited by a transmitted pulse sequence; using the echo data, determine a central tendency of a signal magnitude from regions of adherent microbubbles over time within the region of interest; determine a time series of the signal magnitude; using the time series, determine an initial signal magnitude parameter; obtain a saturated signal parameter and a residual signal parameter using the time series; and determine a relative indication of information indicative of the residual signal magnitude versus the saturated signal magnitude.