IP Library Granted Patent US 10,058,837
Granted Patent B2
US 10,058,837 · App. 13/392,520 · Granted Aug 28, 2018

Systems, methods, and devices for production of gas-filled microbubbles

Inventors: Mark A. Borden (Boulder, CO); Edward J. Swanson (New York, NY)
Assignee: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
B01J13/04A61K49/223
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,058,837
App. No.
13/392,520
Granted
Aug 28, 2018
Kind
B2
Abstract

Gas-filled microbubbles can be synthesized using a continuous flow chamber and a sonicator. The resulting microbubble solution can be size-sorted for a particular application, such as injection into a patient for gas delivery thereto. The microbubble solution may be concentrated to have greater than 50% volume gas while maintaining microbubble sizes below 10 μm. Control of the microbubble generation process can yield highly stable microbubbles. The microbubbles may retain over half of their original gas payload for over three weeks while exhibiting minimal change in microbubble size. The systems, methods, and devices described herein thus allow for continuous or batch-wise continuous production of gas-filled microbubbles that readily release their gas payload when introduced into an under-saturated or de-saturated solution.

Claims (22)

1. A microbubble generation system comprising:

a sonicator member;

a flow chamber surrounding a portion of the sonicator member so as to define a reaction volume between an interior surface of the flow chamber and the surrounded portion of the sonicator member,

the flow chamber having a first inlet, a second inlet, and a first outlet, configured to permit a lipid solution to flow into the reaction volume through the first inlet, and a gas to flow into the reaction volume through the second inlet, and further to permit microbubbles generated in the reaction volume to be removed from the first outlet,

an end of the sonicator member being arranged so as to deliver ultrasonic energy to an interface between the lipid solution and the gas in the reaction volume; and

a level sensor configured to detect a level of the lipid solution in the flow chamber;

a controller configured to control the lipid solution flow into the first inlet responsively to an output of the level sensor so as to maintain a location of said interface with respect to said end of the sonicator member such that the sonicator member is immersed in lipid solution to a level that is above an end of the sonicator member by no more than three times a gap between the end of the sonicator member and a wall of the flow chamber directly opposite the end of the sonicator member.

2. The microbubble generation system of claim 1 , further comprising a size separation module that sorts microbubbles removed from the reaction volume via the first outlet responsively to a size thereof,

wherein the size separation module is configured to isolate microbubbles having a diameter less than 10 μm from the micro bubbles removed from the reaction volume, and

the size separation module is configured to sort microbubbles using differential flotation.

3. The microbubble generation system of claim 2 , wherein the size separation module includes a container with movable partitions arranged at different locations therein, the partitions being configured to form isolated compartments in the container.

4. The microbubble generation system of claim 1 , further comprising a size separation module that sorts microbubbles removed from the reaction volume via the first outlet responsively to a size thereof,

wherein the size separation module includes a flexible bag and a machine with a plurality of clamps arranged at different locations along the bag,

the clamps being configured to clamp the flexible bag at their respective locations so as to form isolated compartments in the flexible bag,

the isolated compartments include first and second compartments for isolating micro bubbles of different size ranges,

the machine has a controller that is configured to first activate the clamps to isolate microbubbles of a predefined size range and subsequently isolate microbubbles that are compacted to predefined degree, and

the machine is configured to centrifuge the flexible bag.

5. The microbubble generation system of claim 4 , wherein the flexible bag includes at least one port, each port providing access to one of the isolated compartments in the flexible bag.

6. The microbubble generation system of claim 1 , further comprising a concentration module configured to concentrate the microbubbles,

wherein concentration module is configured to concentrate the microbubbles so as to have a concentration of at least 50% volume of gas, and

the concentration module includes one of a centrifuge and a dialyzer.

7. The microbubble generation system of claim 1 , wherein the first outlet is arranged at a lowest point of the reaction volume and opposite said end of the sonicator member in the reaction volume so as to define a gap therebetween.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 15, 2015
From: COLUMBIA UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 035908/0603 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2012
From: BORDEN, MARK A.; SWANSON, EDWARD J.
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 027942/0429 →
Continuity (3)
Provisional Application 61237892 · Aug 28, 2009
Provisional Application 61371332 · Aug 6, 2010
Related Publication 20120175305A1 · Jul 12, 2012
Cited By (1)
US 12,628,820