IP Library Granted Patent US 11,884,976
Granted Patent B2
US 11,884,976 · App. 16/515,790 · Granted Jan 30, 2024

Resin composition and flow cells incorporating the same

Inventors: Timothy J. Merkel (San Diego, CA); Wayne N. George (London, GB); Andrew A. Brown (Cambridge, GB); Audrey Zak (San Diego, CA); Gianluca Andrea Artioli (Cambridge, GB); Julia Morrison (Grays, GB); Nikolai Romanov (Cambridge, GB); Lorenzo Berti (San Diego, CA); Graham Boud (San Diego, CA)
Assignees: Illumina, Inc.; Illumina Cambridge Limited
C12Q1/6874C08G77/442C08L33/04C08L63/00C09D153/00C09D163/00C12Q1/6876
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Quick Facts
Patent No.
US 11,884,976
App. No.
16/515,790
Granted
Jan 30, 2024
Kind
B2
Abstract

An example of a resin composition includes a free radical curable resin matrix including an acrylate and a siloxane, and a free radical photoinitiator. When cured, the resin composition has low or no autofluorescence when exposed to blue excitation wavelengths ranging from about 380 nm to about 480 nm or green excitation wavelengths ranging from about 510 nm to about 560 nm.

Claims (39)

1. A resin composition, comprising:

a free radical curable resin matrix including an acrylate and a siloxane, the free radical curable resin matrix being selected from the group consisting of 1,3-bis(3-methacryloxypropyl) tetramethyldisiloxane, tetramethyl tetrakis[3-acryloxypropyl]cyclotetrasiloxane, acryloxypropyl methylsiloxane homopolymer, and combinations thereof;

a free radical photoinitiator, the free radical photoinitiator being phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide;

an epoxy resin matrix; and

a photoacid generator.

2. A flow cell, comprising:

a substrate; and

a cured, patterned resin on the substrate, the cured, patterned resin including depressions separated by interstitial regions, and the cured, patterned resin having been formed from the resin composition of claim 1 .

3. The flow cell as defined in claim 2 , further comprising:

a polymer coating in the depressions; and

a primer grafted to the polymer coating.

4. A method of making a flow cell, comprising:

depositing the resin composition of claim 1 on a substrate;

nanoimprinting the deposited resin composition using a working stamp; and

curing the deposited resin composition to form a cured, patterned resin.

5. The resin composition as defined in claim 1 , wherein a weight % ratio of the epoxy resin matrix to the photoacid generator in the resin composition ranges from about 99.8:0.2 to about 90:10.

6. The resin composition as defined in claim 1 , wherein the epoxy resin matrix is selected from the group consisting of:

i) an epoxy functionalized polyhedral oligomeric silsesquioxane (POSS);

ii) trimethylolpropane triglycidyl ether:

iii) tetrakis(epoxycyclohexyl ethyl)tetramethyl cyclotetrasiloxane:

iv) a copolymer of (epoxycyclohexylethyl)methylsiloxane and dimethylsiloxane:

(wherein a ratio of m:n ranges from 8:92 to 10:90);

v) 1,3-bis[2-(3,4-epoxycyclohexyl) ethyl] tetramethyl disiloxane:

vi) 1,3-bis(glycidoxypropyl)tetramethyl disiloxane:

vii) combinations thereof.

7. The resin composition as defined in claim 1 , wherein the photoacid generator is selected from the group consisting of:

i) N-hydroxynaphthalimide triflate:

ii) triarylsulfonium hexafluorophosphate salts, mixed:

iii) triarylsulfonium hexafluoroantimonate salts, mixed:

iv) 1-naphthyl diphenylsulfonium triflate (NDS-TF):

v) (4-phenylthiophenyl)diphenylsulfonium triflate:

vi) bis-(4-methylphenyl)iodonium hexafluorophosphate:

vii) bis(4-tert-butylphenyl)iodonium hexafluorophosphate:

viii) (2-methylphenyl)(2,4,6-trimethylphenyl)iodonium triflate:

xi) bis(2,4,6-trimethylphenyl)iodonium triflate:

x) bis-(4-dedecylphenyl)iodonium hexafluoroantimonate salt:

xi) combinations thereof.

8. The resin composition as defined in claim 1 , further comprising a surfactant selected from the group consisting of a polyethylene sorbitol ester, a polyoxyethylene sorbitol ester, or octylphenol ethoxylate.

9. The resin composition as defined in claim 1 , further comprising a solvent selected from the group consisting of propylene glycol monomethyl ether acetate, toluene, dimethyl sulfoxide, and tetrahydrofuran.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2019
From: MERKEL, TIMOTHY J.; ZAK, AUDREY; BERTI, LORENZO; BOUD, GRAHAM
To: ILLUMINA, INC.
Reel/Frame 051081/0758 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2019
From: GEORGE, WAYNE N.; BROWN, ANDREW A.; ARTIOLI, GIANLUCA ANDREA; MORRISON, JULIA; ROMANOV, NIKOLAI
To: ILLUMINA CAMBRIDGE LIMITED
Reel/Frame 051081/0825 →
Continuity (2)
Provisional Application 62701228 · Jul 20, 2018
Related Publication 20200024661A1 · Jan 23, 2020
Cited By (3)
US 12,287,574 US 12,559,627 US 12,680,942