Contact lens

Patent metadata

Field	Value
Publication number	US-12164182-B2
Application number	US-202117463574-A
Country	US
Kind code	B2
Filing date	Sep 1, 2021
Priority date	Sep 10, 2020
Publication date	Dec 10, 2024
Grant date	Dec 10, 2024

Abstract

The present disclosure provides a contact lens comprising a first colourant which is a blue-blocking colourant having an absorption maximum (λ max ) in the range of from 415 nm to 455 nm and a second colourant, wherein the second colourant is a polymerizable dye having an absorption maximum (λ max ) in the range of from 470 nm to 600 nm, and optionally also comprising a third colourant which is a colourant having an absorption maximum in the range of from greater than 600 nm to 800 nm. A method of making the lens is also provided.

First claim

The invention claimed is:

1. A contact lens comprising a polymeric matrix formed from the polymerization of a polymerizable composition comprising one or more monomers, a first colourant which is a blue-blocking colourant having an absorption maximum (λ max ) in the range of from 415 nm to 455 nm and a second colourant, wherein the second colourant is a polymerizable dye having an absorption maximum (λ max ) in the range of from 470 nm to 600 nm, wherein the first colourant and the second colourant are present in the contact lens, and the second colourant balances the colour of the first colourant such that the contact lens is colourless, grey or blue.

2. The contact lens as claimed in claim 1 in which the second colourant is an anthraquinone dye.

3. The contact lens as claimed in claim 1 in which the second colourant is a dye and contains a chromophore and at least one polymerizable group wherein each polymerizable group is connected to the chromophore by a linking group.

4. The contact lens as claimed in claim 1 in which the second colourant is a dye of formula (1)
Ch-(L-X m ) n   (1)

where Ch is a chromophore, L is a linking group or heteroatom, X is a polymerizable group, m is from 1 to 3 and n is from 1 to 3.

5. The contact lens as claimed in claim 4 in which m=1 and the linking group L is —N(H)—R 1 —, —SR 1 — or —OR 1 — where R 1 is a divalent hydrocarbylene group, which is substituted or unsubstituted by one or more heteroatoms.

6. The contact lens as claimed in claim 4 in which the linking group L comprises a C6 to C14 aryl group, a C1 to C20 alkyl group, or a C7 to C20 aryl-alkyl group.

7. The contact lens as claimed in claim 4 in which the chromophore Ch is an anthraquinone chromophore which comprises from 1 to 3 substituents selected from —F, —Cl, —Br, —I, —OR 2 , —SR 2 , —R 2 , —NO 2 , —CN, —NCO, —NCS, —C(═O)R 2 , —C(═O)OR 2 , —NH 2 , —C(═O)NHR 2 , —C(═O)N(R 2 ) 2 , where each R 2 is independently H or C1 to C20 hydrocarbyl.

8. The contact lens as claimed in claim 1 in which the second colourant is a dye is according to formula (2)

where a and b can each be from 0 to 3 provided that 0≤(a+b)≤3; each A is independently selected from —F, —Cl, —Br, —I, —OR 2 , —SR 2 , —R 2 , —NO 2 , —CN, —NCO, —NCS, —C(═O)R 2 , —C(═O)OR 2 , —NR 2 2 , —C(═O)NHR 2 , —C(═O)N(R 2 ) 2 , where each R 2 is independently H or C1 to C20 hydrocarbyl; c and d can each be from 0 to 3 provided that 1≤(c+d)≤3; L is a divalent linking group; and X is a polymerizable group.

9. The contact lens as claimed in claim 1 in which the second colourant is a dye is according to formula (3) or formula (4):

10. The contact lens as claimed in claim 1 in which the second colourant has an absorption maximum (λ max ) in the range of from 500 nm to 600 nm.

11. The contact lens as claimed in claim 1 in which the first colourant is present in the contact lens in an amount of from about 20 ppm to about 1000 ppm on a dry basis and/or the second colourant is present in the contact lens in an amount of from about 20 ppm to about 1000 ppm on a dry basis.

12. The contact lens as claimed in claim 1 in which the polymerizable composition comprises a total amount of siloxane monomer of about 20 wt. % to about 60 wt. % based on the total weight of all polymerizable ingredients in the polymerizable composition.

13. The contact lens as claimed in claim 1 in which the polymerizable composition comprises a total amount of hydrophilic vinyl-containing monomer of about 20 wt. % to about 60 wt. % based on the total weight of all polymerizable ingredients in the polymerizable composition.

14. The contact lens as claimed in claim 1 which is a hydrogel contact lens.

15. The contact lens as claimed in claim 1 in which the first colourant and the second colourant are autoclave stable such that they do not change colour or intensity of colour upon autoclaving of the contact lens.

16. A packaged contact lens comprising a sealed package containing a packaging solution and a contact lens as claimed in claim 1 .

17. The contact lens as claimed in claim 1 wherein the polymerizable composition further comprises a third colourant that is present in the contact lens, the third colourant being a colourant having an absorption maximum in the range of from above 600 nm but no higher than 800 nm, and the second colourant and third colourant balance the colour of the first colourant such that the contact lens is colourless, grey or blue.

18. The contact lens as claimed in claim 17 in which the third colourant is present in the contact lens in an amount of from about 20 ppm to about 300 ppm on a dry basis.

19. A method of making a contact lens comprising the steps of polymerizing a polymerizable composition comprising one or more monomers, a first colourant which is a blue-blocking colourant having an absorption maximum (λ max ) in the range of from 415 nm to 455 nm and a second colourant, wherein the second colourant is a polymerizable dye having an absorption maximum (λ max ) in the range of from 470 nm to 600 nm,
in a mould to form a lens-shaped polymerization product comprising a polymeric matrix, wherein the second colourant balances the colour of the first colourant such that the contact lens is colourless, grey or blue.

20. The method as claimed in claim 19 which also includes the step of hydrating the lens-shaped polymerization product to form a hydrogel contact lens.

21. The method as claimed in claim 19 which also includes the step of immersing the polymerization product or the hydrogel contact lens in a package containing a packaging solution, sealing the package, and sterilizing the sealed package.

22. The method as claimed in claim 19 wherein the polymerizable composition further comprises a third colourant which is a colourant having an absorption maximum in the range of from above 600 nm but no higher than 800 nm, and the second colourant and the third colourant balance the colour of the first colourant such that the contact lens is colourless, grey or blue.

Assignees

• Coopervision Int Ltd

Inventors

• Broad Robert Andrew
• Liu Yuwen
• Mitchell William

Classifications

• G02C7/108

  Colouring materials · CPC title

• G02B1/043 Primary

  Contact lenses · CPC title

• C09B1/5035

  only amino and hydroxy groups · CPC title

• C09B1/205

  Dyes with an unsaturated C on the N atom attached to the nucleus (C=O and C=S, C09B1/36) · CPC title

• B29K2105/0032

  Pigments, colouring agents or opacifiyng agents · CPC title