IP Library Granted Patent US 12,478,965
Granted Patent B2
US 12,478,965 · App. 17/340,581 · Granted Nov 25, 2025

Cavity acoustic transducer (CAT) for shear-induced cell transfection

Inventors: Abraham P. Lee (Irvine, CA); Mohammad Aghaamoo (Irvine, CA); Xuan Li (Irvine, CA); Neha Garg (Irvine, CA); Yu-Hsi Chen (Irvine, CA)
Assignee: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
B01L3/502761B01L3/502715B01L3/50273B01L3/502769C12N15/87B01L2200/0668B01L2200/18B01L2300/0645B01L2300/0809B01L2400/0415B01L2400/0436B01L2400/0439
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 12,478,965
App. No.
17/340,581
Granted
Nov 25, 2025
Kind
B2
Abstract

The present invention features the use of cavity acoustic transducers (CATs) to apply mechanical stimuli on cells. CATs utilize the generated acoustic microstreaming vortices to trap cells and apply tunable shear on them. The present invention may use such a portable, automated, and high throughput device for cell transfection.

Claims (33)

1 . A high-throughput transfection method, comprising:

a. providing a microfluidic platform ( 110 ) comprising a main microfluidic channel ( 120 ), and one or more cavity acoustic transducers (CATs) ( 130 ), wherein the one or more CATs ( 130 ) are dead-end channels coupled to the main microfluidic channel ( 120 ), wherein the microfluidic platform ( 110 ) is coupled to an external acoustic source ( 140 );

b. flowing a fluid ( 150 ) through the main microfluidic channel ( 120 ), wherein the fluid ( 150 ) intersects the CATs ( 130 ) to form one or more interfaces ( 180 ); and

c. applying acoustic energy to the CATs ( 130 ) via the external acoustic source ( 140 ) to oscillate the interfaces ( 180 ), wherein oscillating the interfaces ( 180 ) produces a plurality of microstreaming vortices ( 190 ) that causes shear-induced mechanical deformation.

2 . The method of claim 1 , additionally comprising:

a. providing an array of electrodes ( 200 ), the electrodes interdigitated with the microfluidic platform ( 110 ); and

b. applying a voltage to the electrodes ( 200 ) so as to achieve electroporation.

3 . The method of claim 1 , wherein the oscillation is controlled by a piezoelectric transducer (PZT) voltage.

4 . The method of claim 1 , wherein the CAT ( 130 ) induces pumping of the fluid ( 150 ), thereby eliminating a need for external pumping.

5 . The method of claim 1 , wherein the fluid ( 150 ) comprises a cell ( 160 ) and an exogenous material ( 170 ).

6 . The method of claim 1 , wherein a configuration of the CATs ( 130 ) is selected from a group comprising lateral to the main channel ( 120 ), above the main channel ( 120 ), below the main channel ( 120 ), and a combination thereof.

7 . The method of claim 1 , wherein the interfaces ( 180 ) comprise a gas-liquid interface, a liquid-liquid interface, a lipid membrane, a polymer membrane, a nano-particle membrane, or a combination thereof.

8 . A system ( 100 ) for delivery of an exogenous material, the system comprising:

a. a microfluidic platform ( 110 ) comprising a main microfluidic channel ( 120 ), and one or more cavity acoustic transducers (CATs) ( 130 ), wherein the one or more CATs ( 130 ) are dead-end channels coupled to the main microfluidic channel ( 120 ), wherein the microfluidic platform ( 110 ) is coupled to an external acoustic source ( 140 ); and

b. a fluid ( 150 ) disposed through the main microfluidic channel ( 120 ), wherein the fluid ( 150 ) intersects the CATs ( 130 ) to form one or more interfaces ( 180 );

wherein the CATs ( 130 ) are configured to oscillate the interfaces ( 180 ) to produce a plurality of microstreaming vortices ( 190 ) that causes shear-induced mechanical deformation.

9 . The system of claim 8 , wherein the system ( 100 ) additionally comprises an array of electrodes ( 200 ), the electrodes interdigitated with the microfluidic platform ( 110 ), and wherein the electrodes ( 200 ) are configured to promote electroporation ( 160 ) when a voltage is applied to the electrodes ( 200 ).

10 . The system of claim 8 , wherein the oscillation is controlled by a piezoelectric transducer (PZT) voltage.

11 . The system of claim 8 , wherein the CAT ( 130 ) is configured to induce pumping of the fluid ( 150 ), thereby eliminating the need for external pumping.

12 . The system of claim 8 , wherein the fluid ( 150 ) comprises a cell ( 160 ) and the exogenous material.

13 . The system of claim 8 , wherein a configuration of the CATs ( 130 ) is selected from a group comprising lateral to the main channel ( 120 ), above the main channel ( 120 ), below the main channel ( 120 ), and a combination thereof.

14 . The system of claim 8 , wherein the interfaces ( 180 ) comprise a gas-liquid interface, a liquid-liquid interface, a lipid membrane, a polymer membrane, a nano-particle membrane, or a combination thereof.

15 . A high-throughput transfection method, comprising:

a. providing a microfluidic platform ( 110 ) comprising a main microfluidic channel ( 120 ), and one or more cavity acoustic transducers (CATs) ( 130 ), wherein the one or more CATs ( 130 ) are dead-end channels coupled to the main microfluidic channel ( 120 ), wherein the microfluidic platform ( 110 ) is coupled to an external acoustic source ( 140 );

b. providing an array of electrodes ( 200 ), the electrodes interdigitated with the microfluidic platform ( 110 );

c. flowing a fluid ( 150 ) through the main microfluidic channel ( 120 ), wherein the fluid ( 150 ) intersects the CATs ( 130 ) to form one or more interfaces ( 180 );

d. applying acoustic energy to the CATs ( 130 ) via the external acoustic source ( 140 ) to oscillate the interfaces ( 180 ), wherein oscillating the interfaces ( 180 ) produces a plurality of microstreaming vortices ( 190 ) that causes shear-induced mechanical deformation; and

e. applying a voltage to the electrodes ( 200 ) so as to achieve electroporation, wherein the electrodes are capable of at least a first mode and a second mode, wherein the first mode achieves generation of pores and the second mode achieves widening of said pores generated in the first mode.

16 . The method of claim 15 , wherein the oscillation is controlled by a piezoelectric transducer (PZT) voltage.

17 . The method of claim 15 , wherein the CAT ( 130 ) induces pumping of the fluid ( 150 ), thereby eliminating the need for external pumping.

18 . The method of claim 15 , wherein the fluid ( 150 ) comprises a cell ( 160 ) and an exogenous material.

19 . The method of claim 15 , wherein a configuration of the CATs ( 130 ) is selected from a group comprising lateral to the main channel ( 120 ), above the main channel ( 120 ), below the main channel ( 120 ), and a combination thereof.

20 . The method of claim 15 , wherein the interfaces ( 180 ) comprise a gas-liquid interface, a liquid-liquid interface, a polymer membrane, a nano-particle membrane, or a combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2024
From: LEE, ABRAHAM P.; AGHAAMOO, MOHAMMAD; LI, XUAN; GARG, NEHA; CHEN, YU-HSI
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 069665/0416 →
Continuity (3)
Continuation In Part 16547152 · Aug 21, 2019
Provisional Application 62720829 · Aug 21, 2018
Related Publication 20210291185A1 · Sep 23, 2021
References Cited (7)
US 9517465B2 · Patel et al. · 2016 [cited by applicant]
US 11052395B2 · Lee · 2021 [cited by examiner]
US 20180016539A1 · Ding et al. · 2018 [cited by applicant]
WO WO2016077761A1 · 2016 [cited by applicant]
Tovar et al. “Lateral cavity acoustic transducer.” Twelfth International Conference on Miniaturized Systems for Chemistry and Life Sciences Oct. 12-16, 2008, San Diego, California, USA. 1384-1386. [cited by applicant]
Garg, N. et al. Whole-Blood Sorting. Enrichment and in situ Immunolabeling of Cellular Subsets Using Acoustic Microstreaming. Microsystems & Nanoengineering. Feb. 26, 2018, vol. 4.17085. DOI:10.1038/micronano.2017.85. [cited by applicant]
Nivedita et al., A high throughput microfluidic platform for size-selective enrichment of cell populations in tissue and blood samples, 2017, Ananlyst, 2558-2569 (Year: 2017). [cited by applicant]