Perforated tissue matrix
US-2024408277-A1 · Dec 12, 2024 · US
US2015306562A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2015306562-A1 |
| Application number | US-201514792877-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 7, 2015 |
| Priority date | Apr 2, 2010 |
| Publication date | Oct 29, 2015 |
| Grant date | — |
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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.
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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.
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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