IP Library Granted Patent US 10,525,436
Granted Patent B2
US 10,525,436 · App. 15/208,606 · Granted Jan 7, 2020

Neutralization and containment of redox species produced by circumferential electrodes

Inventors: Karl Maurer (Everett, WA); John J Cooper, Jr. (Seattle, WA); H Sho Fujii (Seattle, WA); Joseph Leonetti (Daly City, CA)
Assignee: CustomArray, Inc.
B01J19/0046B82Y30/00C25B3/10C25B9/06C25B11/02B01J2219/00527B01J2219/00529B01J2219/00576B01J2219/00585B01J2219/00596B01J2219/00641B01J2219/00653B01J2219/00659B01J2219/00675B01J2219/00713B01J2219/00722B01J2219/00725B01J2219/00731B01J2219/00736
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 10,525,436
App. No.
15/208,606
Granted
Jan 7, 2020
Kind
B2
Abstract

There is disclosed an electrode array architecture employing continuous and discontinuous circumferential electrodes. There is further disclosed a process for the neutralization of acid generated at anode(s) by base generated at cathode(s) circumferentially located to each other so as to confine a region of pH change. The cathodes can be displayed as concentric rings (continuous) or as counter electrodes in a cross pattern (discontinuous). In this way reagents, such as acid, generated in a center electrode are countered (neutralized) by reagents, such as base, generated at the corners or at the outer ring.

Claims (42)

1. A method for electrochemical oligomer synthesis on a dense electrode array comprising:

(a) providing a dense electrode array including a plurality of cells and a surface, where each cell of the plurality of cells includes an anode and a circumferential cathode, where each of the anodes are separately addressable electrodes, where a porous reaction layer is adsorbed to the surface, where the porous reaction layer is formed from one or more materials selected from the group consisting of a disaccharide, and a monosaccharide;

(b) contacting the porous reaction layer with a bathing solution; and

(c) bonding a first nucleotide having at least one protected chemical functional group to the porous reaction layer;

(d) conducting a deblocking step by addressing each active anode with a first current or a first voltage to generate an acid, where each active anode is surrounded by a cathode that is biased with a second current or a second voltage, where the cathode produces a base to neutralize the acid, where the cathode is separated from each active anode by an electrode margin, where an insulating material is present in the electrode margin, where the at least one protected chemical functional group is removed by the action of the acid forming at least one deprotected chemical functional group; and

(e) bonding a second nucleotide having at least one protected chemical functional group to the at least one deprotected chemical functional group.

2. The method of claim 1 , where step (d) addresses each active anode with the first current.

3. The method of claim 1 , where step (d) addresses the cathode with the second current.

4. The method of claim 1 , where at least two neighboring electrodes are arranged in a pattern selected from the group consisting of nearest neighbor, neighbor electrodes, border of neighbor electrodes, border of nearest-neighbor, one closest available electrode, and electrode that is not approach.

5. The method of claim 1 , where the insulating material is no more than 10 microns from the outer edge of each anode to the inner edge of the cathode.

6. A method for electrochemical oligomer synthesis on a dense electrode array comprising:

(a) providing a dense electrode array including a plurality of cells and a surface, where each cell of the plurality of cells includes an anode and a cathode, where the cathode forms an outer ring around each anode, where each of the anodes are separately addressable, where a porous reaction layer comprising a disaccharide and/or a monosaccharide is adsorbed to the surface;

(b) applying a bathing solution to the porous reaction layer;

(c) bonding a first nucleotide having at least one protected chemical functional group to the porous reaction layer;

(d) addressing one or more anodes with a first current or a first voltage to generate an acid;

(e) applying a second current or a second voltage to the cathode to generate a base, where the base neutralizes the acid, where the cathode is separated from each active anode by an electrode margin, where an insulating material is present in the electrode margin, where the at least one protected chemical functional group is removed by the action of the acid forming at least one deprotected chemical functional group; and

(f) bonding a second nucleotide having at least one protected chemical functional group to the at least one deprotected chemical functional group.

7. The method of claim 6 , where the thickness of the insulating material is between:

a lower limit of 10 microns; and

an upper limit of 50 microns.

8. The method of claim 6 , where an outer edge of the outer ring of a first cell is separated from an outer edge of the outer ring of a second cell by between:

a lower limit of 33 microns; and

an upper limit of 50 microns.

9. The method of claim 6 , where the cell diameter is 44 microns.

10. The method of claim 6 , where a center point of a first cell is separated from a center point of a second cell by 75 microns.

11. The method of claim 6 , where step (d) addresses each active anode with the first current.

12. The method of claim 6 , where step (e) applies the second current to the cathode.

13. A method for electrochemical oligomer synthesis on a dense electrode array comprising:

(a) providing a dense electrode array including a plurality of cells and a surface, where each cell of the plurality of cells includes a cathode and an anode, where the anode forms an outer ring around each cathode, where each of the cathodes are separately addressable, where a porous reaction layer comprising a disaccharide and/or a monosaccharide is adsorbed to the surface;

(b) applying a bathing solution to the porous reaction layer;

(c) bonding a first nucleotide having at least one protected chemical functional group to the porous reaction layer;

(d) addressing one or more cathodes with a first current or a first voltage to generate a base;

(e) applying a second current or a second voltage to the anode to generate an acid, where the acid neutralizes the base, where the anode is separated from each active cathode by an electrode margin, where an insulating material is present in the electrode margin, where the at least one protected chemical functional group is removed by the action of the acid forming at least one deprotected chemical functional group; and

(f) bonding a second nucleotide having at least one protected chemical functional group to the at least one deprotected chemical functional group.

14. The method of claim 13 , where the thickness of the insulating material is between:

a lower limit of 10 microns; and

an upper limit of 50 microns.

15. The method of claim 13 , where an outer edge of the outer ring of a first cell is separated from an outer edge of the outer ring of a second cell by between:

a lower limit of 33 microns; and

an upper limit of 50 microns.

16. The method of claim 13 , where the cell diameter is 44 microns.

17. The method of claim 13 , where a center point of a first cell is separated from a center point of a second cell by 75 microns.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2017
From: LEONETTI, JOSEPH
To: COMBIMATRIX CORPORATION
Reel/Frame 043815/0849 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2017
From: COMBIMATRIX CORPORATION
To: CUSTOMARRAY, INC.
Reel/Frame 044167/0517 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2017
From: COMBIMATRIX CORPORATION
To: CUSTOMARRAY, INC.
Reel/Frame 043311/0847 →
Continuity (2)
Division 11108078 · Apr 15, 2005
Related Publication 20160354751A1 · Dec 8, 2016
Cited By (1)
US 12,686,950