Adjustable chromophore compounds and materials incorporating such compounds

US2015306562A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2015306562-A1
Application numberUS-201514792877-A
CountryUS
Kind codeA1
Filing dateJul 7, 2015
Priority dateApr 2, 2010
Publication dateOct 29, 2015
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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The present invention is directed to adjustable chromophore compounds and materials (e.g., ophthalmic lens materials) incorporating those compounds. The adjustable chromophore compounds include a chemical moiety that structurally changes upon exposure to predetermined electromagnetic radiation (e.g., two photon radiation) as well as lens materials, particularly intraocular lens materials that incorporate those compounds.

First claim

Opening claim text (preview).

1 - 21 . (canceled) 22 . A method of adjusting a lens, the method comprising: providing a lens having a compound of the formula: B—X; wherein: i) B is a base chromophore compound; and ii) X is an adjustable chemical moiety; exposing the compound B—X to predetermined electromagnetic radiation thereby forming the compound: B—C; wherein: i) the compound B—C provided greater light absorption than the compound B—X; and ii) the remaining chemical moiety (C) includes a conjugated double bond. 23 . A method as in claim 22 wherein the base chromophore compound is selected from the group consisting of benzotriazoles, benzophenones, azo dyes and cinnamate esters. 24 . A method as in claim 23 wherein the base chromophore compound is a benzotriazole. 25 . A method as in claim 23 wherein the compound B—C absorbs a significant amount of UV light, blue light or both. 26 . A method as in claim 25 wherein the compound B—C absorbs a significant amount of blue light. 27 . A method as in claim 23 wherein the adjustable chemical moiety X is a cyclic moiety. 28 . A method as in claim 23 wherein the adjustable chemical moiety X is dicyclopentadiene. 29 . A method as in claim 22 wherein: i) the lens is formed of a polymeric material; ii) the adjustable chromophore compound is distributed within the polymeric material; and iii) the polymeric material can absorb light at progressively greater wavelengths as greater amounts of the compound B—C are formed from the adjustable compound B—X. 30 . A method as in claim 29 further comprising: implanting the lens within an eye of an individual wherein the step of exposing the compound B—X to the predetermined electromagnetic radiation to form the compound B—C occurs after implanting of the lens in the eye. 31 . A method of adjusting a lens, the method comprising: providing a lens having a compound of the formula: B—X or B—C as part of the reactive system: B—X⇄B—C wherein: i) B is a base chromophore compound; ii) X is an adjustable chemical moiety that forms remaining chemical moiety (C) upon exposure to first predetermined electromagnetic radiation thereby forming the compound B—C; iii) the compound B—C provides greater light absorption than the compound B—X; and iv) the remaining chemical moiety (C) includes a conjugated double bond; and v) the compound B—C forms the compound B—X upon exposure to second predetermined electromagnetic radiation either with or without the aid of a separable group (S)and exposing either: i) the compound B—X to the first predetermined electromagnetic radiation to form the compound B—C; or ii) the compound B—C to the second predetermined electromagnetic radiation to form the compound B—X. 32 . A method as in claim 31 wherein the base chromophore compound is selected from the group consisting of benzotriazoles, benzophenones, azo dyes and cinnamate esters. 33 . A method as in claim 32 wherein the base chromophore compound is a benzotriazole. 34 . A method as in claim 31 wherein the compound B—C absorbs a significant amount of blue light. 35 . A method as in claim 32 wherein the adjustable chemical moiety X is a cyclic moiety. 36 . A method as in claim 35 wherein the adjustable chemical moiety X is dicyclopentadiene.

Assignees

Inventors

Classifications

  • Sunlight; Visible light · CPC title

  • Contact lenses · CPC title

  • with aryl radicals directly attached in position 2 · CPC title

  • condensed with carbocyclic rings · CPC title

  • for reconstruction of eye parts, e.g. intraocular lens, cornea · CPC title

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What does patent US2015306562A1 cover?
The present invention is directed to adjustable chromophore compounds and materials (e.g., ophthalmic lens materials) incorporating those compounds. The adjustable chromophore compounds include a chemical moiety that structurally changes upon exposure to predetermined electromagnetic radiation (e.g., two photon radiation) as well as lens materials, particularly intraocular lens materials that i…
Who is the assignee on this patent?
Novartis Ag
What technology area does this patent fall under?
Primary CPC classification A61L27/50. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Oct 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).