IP Library › Granted Patent US 10,695,737
Granted Patent B2
US 10,695,737 · App. 15/643,732 · Granted Jun 30, 2020

Patterning device

Inventors: Jeroen Lammertyn (Neerijse, BE); Daan Witters (Geetbets, BE)
Assignee: Katholieke Universiteit Leuven, K.U.Leuven R&D
B01J19/0046B01L3/502707B01L3/502792B01J2219/0065B01J2219/00382B01J2219/00387B01J2219/00619B01L2200/0668B01L2200/0673B01L2200/142B01L2300/0636B01L2300/0816B01L2300/161B01L2400/043B01L2400/0427B82Y30/00
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Quick Facts
Patent No.
US 10,695,737
App. No.
15/643,732
Granted
Jun 30, 2020
Kind
B2
Abstract

A novel miniaturized and highly automated method for the controlled printing of large arrays of nano- to femtoliter droplets is presented by actively transporting mother droplets over hydrophilic-in-hydrophobic micropatches. The proposed technology consists of single plate or double-plate devices where mother droplets can be actuated and hydrophilic-in-hydrophobic micropatches on one or both plates of the device where nano- to femtoliter droplets are printed. Due to the selective wettability of the more wettable hydrophilic micropatches in a hydrophobic matrix, large nano- to femtoliter droplet arrays are created when mother droplets are transported over these arrays. The parent droplets can be moved by different droplet actuation principles, for example, by using the principle of electrowetting-on-dielectric droplet actuation. We propose another method that uses two plates that are placed on top of each other while being separated by a spacer. One plate is dedicated to confirming and guiding of parent droplets by using hydrophilic patches in a hydrophobic matrix, while the other plate contains hydrophilic-in-hydrophobic arrays dedicated to the printing of nano- to femtoliter droplets. When the plate dedicated to parent droplet guiding is rotated over the plate dedicated to printing of nano- to femtoliter droplets, nano- to femtoliter droplets are dispensed inside the hydrophilic-in-hydrophobic array due to their selective wettability. All these proposed methods allow the parent droplets to be moved over the hydrophilic-in-hydrophobic arrays many times, providing unique advantages for performing bio-assays or miniaturized materials synthesis in nano- to femtoliter sized droplets. Upon the controlled evaporation of the dispensed droplets of solution, large arrays of the printed material can be generated on an automated way in seconds of time on a very flexible way. The method disclosed herein provides a distinct nano- to femtoliter droplet printing technique for a wide variety of applications such as protein- or cell-based bio-assays or printing of crystalline structures, suspensions of nanoparticles or components for microelectronics.

Claims (41)

1. A system for printing an array of liquid droplets, the system comprising:

a droplet actuation mechanism comprising at least one plate having a plurality of actuation electrodes; and

a hydrophobic surface having an array of microwells therein, each microwell having a volume from 10 −15 liters to 10 −9 liters;

wherein the plurality of actuation electrodes are configured to transport a parent droplet along a path proximate a region of the array of microwells to form an array of liquid droplets, wherein each liquid droplet corresponds to a microwell in the region proximate the path and has a volume from 10 −15 liters to 10 −9 liters.

2. The system of claim 1 , wherein the actuation electrodes are configured to transport the parent droplet by electrowetting-on-dielectric based droplet actuation.

3. The system of claim 1 , wherein the hydrophobic surface comprises a fluoropolymer.

4. The system of claim 1 , further comprising a hydrophilic layer underlying the hydrophobic surface.

5. The system of claim 4 , wherein the hydrophilic layer comprises a dielectric layer.

6. The system of claim 1 , wherein each microwell has a diameter of 1 to 1000 micrometers.

7. The system of claim 1 , wherein at least one of the microwells is configured to include a fluorophore resulting from a polymerase chain reaction.

8. The system of claim 1 , further comprising the array of liquid droplets, wherein at least one liquid droplet of the array of liquid droplets includes at least one microbead disposed therein.

9. The system of claim 8 , wherein the at least one microbead is configured to capture a biomolecule to undergo a digital enzyme-linked immunosorbent assay.

10. The system of claim 8 , wherein the at least one microbead has a paramagnetic attraction toward the array of microwells.

11. The system of claim 1 , wherein the hydrophobic surface is curved.

12. The system of claim 1 , wherein the at least one plate comprises a first plate and a second plate, the droplet actuation mechanism further comprising a spacer separating the first plate from the second plate.

13. The system of claim 12 , wherein the plurality of actuation electrodes are disposed on at least one of the first plate and the second plate.

14. The system of claim 12 , wherein the first plate is spaced from the second plate a distance of 1 to 1000 micrometers.

15. The system of claim 12 , further comprising an oil disposed between the first plate and the second plate to reduce or prevent evaporation of the parent droplet.

16. The system of claim 1 , wherein the array of microwells is configured to form the array of liquid droplets for at least one of an immunological assay, a digital enzyme-linked immunosorbent assay, and digital polymerase chain reaction.

17. The system of claim 1 , wherein the hydrophobic surface comprises a nucleic acid library joined thereto by at least one hybridization probe.

18. The system of claim 1 , further comprising a dielectric layer disposed on the plurality of actuation electrodes.

19. A system for printing an array of liquid droplets, the system comprising:

a droplet actuation mechanism comprising: a first plate, a second plate, and a spacer separating the first plate from the second plate, both the first plate and second plate having a plurality of actuation electrodes disposed thereon; and

a hydrophobic surface having an array of microwells therein, each microwell having a volume from 10 −15 liters to 10 −9 liters;

wherein the plurality of actuation electrodes are configured to transport a parent droplet along a path proximate a region of the array of microwells to form an array of liquid droplets, and

wherein each liquid droplet corresponds to a microwell in the region proximate the path and has a volume from 10 −15 liters to 10 −9 liters.

20. A system for printing an array of liquid droplets, the system comprising:

a droplet actuation mechanism comprising at least one plate having a plurality of actuation electrodes; and

a hydrophobic surface having an array of microwells therein, each microwell having a volume from 10 −15 liters to 10 −9 liters;

wherein the plurality of actuation electrodes are configured to transport a parent droplet along a path proximate a region of the array of microwells to form the array of liquid droplets,

wherein each liquid droplet corresponds to a microwell in the region proximate the path and has a volume from 10 −15 liters to 10 −9 liters, and

wherein at least one liquid droplet of the array of liquid droplets includes at least one microbead disposed therein.

21. The system of claim 20 , wherein the at least one microbead is configured to capture a biomolecule to undergo a digital enzyme-linked immunosorbent assay.

22. The system of claim 20 , wherein the at least one microbead has a paramagnetic attraction toward the array of microwells.

23. A system for printing an array of liquid droplets, the system comprising:

a droplet actuation mechanism comprising at least one plate having a plurality of actuation electrodes;

a fluid reservoir in fluid communication with the droplet actuation mechanism; and

a hydrophobic surface having an array of microwells therein, each microwell having a volume from 10 −15 liters to 10 −9 liters; and

wherein the plurality of actuation electrodes are configured to transport a parent droplet along a path proximate a region of the array of microwells to form an array of liquid droplets,

wherein the parent droplet is generated from the fluid reservoir, and

wherein each liquid droplet corresponds to a microwell in the region proximate the path and has a volume from 10 −15 liters to 10 −9 liters.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2017
From: LAMMERTYN, JEROEN; WITTERS, DAAN
To: KATHOLIEKE UNIVERSITEIT LEUVEN, K.U.LEUVEN R&D
Reel/Frame 042930/0818 →
Priority Claims (3)
GB 1201277.9 · Jan 24, 2012 · national
GB 1218994.0 · Oct 23, 2012 · national
GB 1218995.7 · Oct 23, 2012 · national
Continuity (4)
Continuation 14374499
Provisional Application 61725268 · Nov 12, 2012
Provisional Application 61592399 · Jan 30, 2012
Related Publication 20180015437A1 · Jan 18, 2018
Cited By (1)
US 12,730,300