IP Library Granted Patent US 10,105,350
Granted Patent B2
US 10,105,350 · App. 15/125,558 · Granted Oct 23, 2018

Cosmetic preservatives as therapeutic corneoscleral tissue cross-linking agents

Inventors: David Choohyun Paik (Cheltenham, PA); Stephen Lewis Trokel (New York, NY)
Assignee: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
A61K31/4166A61K31/115A61K31/4178A61K33/00C07K14/78
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 10,105,350
App. No.
15/125,558
Granted
Oct 23, 2018
Kind
B2
Abstract

A method of cross-linking collagen present in a collagenous tissue comprising contacting the collagenous tissue with an amount of a formaldehyde releasing agent effective to crosslink the collagen is provided. A method of inhibiting loss of structural integrity of a collagenous tissue during transplantation-related transport comprising contacting the collagenous tissue with an amount of a formaldehyde releasing agent effective to inhibit loss of structural integrity of the collagenous tissue is also provided. A composition for ophthalmic administration comprising a formaldehyde releasing agent, sodium bicarbonate, and ophthalmically suitable carriers or excipients is also provided. Finally, a method of altering the refractive power of a cornea comprising contacting the cornea with a formaldehyde releasing agent so as to effect cross-linking in the cornea and thereby alter the refractive power of the cornea is provided.

Claims (11)

1. A method of cross-linking collagen present in a collagenous tissue comprising contacting the collagenous tissue with an amount of a formaldehyde releasing agent effective to cross-link the collagen, wherein the formaldehyde releasing agent is 1-(phenylmethoxy)-methanol, N-hydroxymethyl-N-(1,3-di(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl)-N′-hydroxy-methylurea, 1,3-dimethylol-5,5-dimethyl-hydantoin, N,N′-methylenebis[N-[3-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl]]-urea, sodium hydroxymethyl glycinate, 5-bromo-5-nitro-1,3-dioxane, 2-bromo-2-nitropropane-1,3-diol, 3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane,1-(3-chloro-2-propen-1-yl)-chloride(1:1), 4,5-dihydroxy-1,3-dimethyl-2-Imidazolidinone, 4,5-dihydroxy-1,3-bis(hydroxymethyl)-2-Imidazolidinone, tetrahydro-1,3-bis(hydroxymethyl)-2(1H)-pyrimidinone, tetrahydro-1,3,4,6-tetrakis(hydroxymethyl)-imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, polyoxymethylene urea, 4,4-dimethylyoxazolidine, 7a-ethyldihydro-1H,3H,5H-oxazolo[3,4-c]oxazole, 4,5-dihydroxy-1,3-bis(hydroxymethyl)-2-imidazolidinone methylated, dimethylhydantoin formaldehyde resin, 4,5-dihydroxy-1,3-bis(hydroxymethyl)-2-imidazolidinone, 1,3-bis(hydroxymethyl)-2-imidazolidinone, N,N′-bis(hydroxymethyl)-urea, 1,3-ethyleneurea, (Z)-3-(bis(2-hydroxyethyl)amino)-2-(2-hydroxyethyl-(hydroxymethyl)amino) prop-2-en-1-ol, 1,3,5-trietethyl-1,3,5-tiazinane, 4,5-dihydroxy-2-imidazolidinone, 1-(hydroxymethyl)-5,5-dimethyl-2,4-Imidazolidinedione, 1,3,5,7-tetraazatricyclo[3.3.1.13,7]decane, 4,4′-methylenebis-morpholine, 2-chloro-N-(hydroxymethyl)-acetamide, N-(hydroxymethyl)-urea, polyoxymethylene melamine, 1,1′-[methylenebis(oxymethylene)]bis-benzene, 1,6-dihydroxy-2-5-dioxahexane (1,1′-[1,2-ethanediylbis(oxy)]bis-methanol, 2,4-imidazolidinedione, hydroxymethyl-5-5-dimethyl-2-4-imidazolidinedione, 3-hydroxymethyl-5-5-dimethylimidazolidine-2,4-dione, dimethoxy-methane, N-methylolethanolamine, 1H,3H,5H-oxazolo[3,4-c]oxazole-7a(7H)-methanol, Bioban N-95 (mixture of 5-methyl-1-aza-3,7-dioxabicyclo[3.3.0]octane, 5-hydroxymethoxymethyl-1-aZa-3,7-diox abicyclo[3.3.0]octane, and higher hydroxyalkoxymethyl oligomers), 5-methyl-1-aza-3,7-dioxabicyclo[3.3.0]octane, 4,4-dimethyl-oxazolidine, 4-ethyl-2-(1-methylethyl)-oxazolidine, 2-(hydroxymethyl)-2-nitro-1,3-propanediol, diethylamine/2-methyl-2 nitro-1,3-propanediol, dimethylamine-2-methyl-2-nitro-1,3-propanediol, pyrrolidine/2-methyl 2-nitro-1,3-propanediol, 2-furfural/2-methyl 2-nitro-1,3-propanol, N-hydroxy-2-propanamine, N-hydroxy-1-propanamine, N-hydroxy-ethanamine, N-hydroxy-2-methyl-2-propanamine, N-hydroxy-cyclohexanamine, N-ethyl-N-hydroxy-ethanamine, 1,1′-[methylenebis(oxy)]bis[2-methyl-2-nitro-(9CI)]-propane, hydroxylamine (HA) nitrone, N-ethylhydroxylamine (EHA) nitrone, N-propylhydroxylamine (PHA) nitrone, N-t-butyl hydroxylamine (tBuHA) nitrone, Cyclohexanedicarboxaldehyde (CHDA)-bis-isopropylhydroxylamine (IPHA) nitrone, N-benzyl hydroxylamine (N-BzHA) nitrone, or vanillin-isopropylhydroxylamine (IPHA) nitrone.

2. The method of claim 1 wherein the formaldehyde releasing agent is 1-(phenylmethoxy)-methanol, N-hydroxymethyl-N-(1,3-di(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl)-N′-hydroxy-methylurea, 1,3-dimethylol-5,5-dimethyl-hydantoin, N,N′-methylenebis[N-[3-(hydroxymethyl)-2,5-dioxo-4-imidazolidinyl]]-urea, sodium hydroxymethyl glycinate, or 5-methyl-1-aza-3,7-dioxabicyclo[3.3.0]octane.

3. The method of claim 1 wherein the formaldehyde releasing agent is N-hydroxymethyl-N-(1,3-di(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl)-N′-hydroxy-methylurea.

4. The method of any of claim 1 wherein the formaldehyde releasing agent is present in a solution.

5. The method of any of claim 1 wherein the formaldehyde releasing agent is in an aqueous solution having a pH effective for cross-linking.

6. The method of claim 5 wherein the pH is 7.4.

7. The method of claim 5 wherein the pH is 8.5.

8. The method of any of claim 5 wherein the formaldehyde releasing agent is present in an aqueous solution comprising sodium bicarbonate.

9. The method of any of claim 1 wherein the contacting of the formaldehyde releasing agent to the collagenous tissue is performed by intermittent administration of the formaldehyde releasing agent to the collagenous tissue for a duration of time effective to cross-link collagen.

10. The method of claim 1 wherein the collagenous tissue is heart valve, blood vessel, cornea, sclera, skin, tendon, fascia, bone, or cartilage.

11. The method of claim 1 wherein the collagenous tissue is cornea of a subject and the subject is afflicted with keratoconus or keratectasia.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 14, 2018
From: PAIK, DAVID CHOOHYUN; TROKEL, STEPHEN LEWIS
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 046874/0531 →
CONFIRMATORY LICENSE Recorded Dec 5, 2016
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040807/0030 →
Continuity (3)
Provisional Application 61952043 · Mar 12, 2014
Provisional Application 62088383 · Dec 5, 2014
Related Publication 20160374992A1 · Dec 29, 2016
Cited By (1)
US 12,396,889