IP Library › Granted Patent US 12,521,324
Granted Patent B2
US 12,521,324 · App. 18/653,623 · Granted Jan 13, 2026

Polyurethane gels

Inventors: Anna K. Croom (Brooklyn, NY); Ronald V. Lerum (Leonia, NJ); John Gormley (Midland Park, NJ); Michael J. Isaacman (New York, NY)
Assignee: GRANT INDUSTRIES, INC.
A61K8/042A61K8/87A61K9/06A61Q19/00C08G18/10C08G18/227C08G18/345C08G18/348C08G18/36C08G18/73C08G18/755A61K2800/48A61K2800/805
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 12,521,324
App. No.
18/653,623
Granted
Jan 13, 2026
Kind
B2
Abstract

The present invention relates to gel compositions comprising a polyurethane elastomer. The polyurethane elastomer is formed from the reaction of a polyol, a polyisocyanate, and a polyurethane reaction catalyst in the presence of a topically acceptable carrier fluid. In some embodiments, the gel composition comprises a personal active ingredient or a healthcare active ingredient, which may be incorporated into the gel composition via a pre-load method or a post-load method. Also provided herein are gel pastes and topical formulations containing the polyurethane elastomers, and methods of making the same.

Claims (28)

1 . A gel composition comprising a polyurethane elastomer gel containing a reaction product of:

(A) a polyisocyanate or a mixture of polyisocyanates comprising two or more isocyanate functional groups;

(B) a polyol or mixture of polyols comprising two or more hydroxyl functional groups;

(C) a polyurethane reaction catalyst; and

(D) a topically acceptable carrier fluid acting as a solvent, the solvent being acceptable for cutaneous surfaces, the topically acceptable carrier being selected from the group consisting of esters, triglycerides, hydrocarbons, oils and combinations thereof;

wherein the reaction product has an elastomeric matrix with the topically acceptable carrier fluid entrapped in the elastomeric matrix; and

wherein the polyurethane elastomer gel is a smooth, non-tacky, homogenous gel.

2 . The gel composition of claim 1 , wherein the topically acceptable carrier fluid comprises a member of the group consisting of diisooctyl succinate, heptyl undecylenate, neopentyl glycol diheptanoate, coco-caprylate/caprate, triheptanoin, caprylic/capric triglyceride, dodecane, tridecane, C13-15 alkanes, squalenes, squalenes, isoamyl laurate, isopentyl laurate, caprylic/capric/myristic/stearic triglyceride, caprylic/capric/succinic triglyceride, isopropyl myristate, jojoba esters, tricaprylin, palm oil and combinations thereof.

3 . The gel composition of claim 1 , further comprising a pharmaceutically active ingredient dissolved in the topically acceptable carrier fluid.

4 . The gel composition of claim 1 , wherein the polyisocyanate or mixture of polyisocyanates is a low molecular weight polyisocyanate or mixture of polyisocyanates and wherein the polyol or mixture of polyols contains two or more hydroxyl, amine, thiol, or carboxylic acid groups.

5 . The gel composition of claim 1 , wherein the polyurethane reaction catalyst is a bismuth group containing catalyst.

6 . The gel composition of claim 1 , wherein greater than 50% of the carbon content of the topically acceptable carrier fluid is derived from a plant source.

7 . A topical formulation comprising:

the gel composition of claim 1 and a pharmaceutically active ingredient, wherein the pharmaceutically active ingredient is a personal care active ingredient or a healthcare active ingredient.

8 . A gel composition comprising a polyurethane elastomer gel containing a reaction product of:

(A) castor oil;

(B) isophorone diisocyanate, wherein the molar ratio of isocyanate groups to hydroxyl groups is from about 1:1 to 1:2;

(C) a polyurethane reaction catalyst; and

(D) a topically acceptable carrier fluid acting as a solvent at a concentration of 60% (w/w) to 99.9% (w/w) of the gel composition, the solvent being acceptable for cutaneous surfaces, the topically acceptable carrier being selected from the group consisting of esters, triglycerides, hydrocarbons, oils and combinations thereof;

wherein a personal care or healthcare active ingredient is optionally incorporated into the polyurethane elastomer gel by dissolving the personal care or healthcare active ingredient in the topically acceptable carrier fluid during formation of the polyurethane elastomer gel, or by admixing the personal care or healthcare active ingredient with a formed polyurethane elastomer gel;

wherein the reaction product has an elastomeric matrix with the topically acceptable carrier fluid entrapped in the elastomeric matrix; and

wherein the polyurethane elastomer gel is a smooth, non-tacky, homogenous gel.

9 . The gel composition of claim 8 , wherein the topically acceptable carrier fluid is selected from the group consisting of diisooctyl succinate, heptyl undecylenate, neopentyl glycol diheptanoate, coco-caprylate/caprate, and combinations thereof.

10 . The gel composition of claim 8 , further comprising a pharmaceutically active ingredient dissolved in the topically acceptable carrier fluid.

11 . The gel composition of claim 8 , wherein the polyurethane reaction catalyst is a bismuth group containing catalyst.

12 . The gel composition of claim 8 , wherein greater than 50% of the carbon content of the topically acceptable carrier fluid is derived from a plant source.

13 . A topical formulation comprising:

the gel composition of claim 8 and a pharmaceutically active ingredient, wherein the pharmaceutically active ingredient is a personal care active ingredient or a healthcare active ingredient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2024
From: CROOM, ANNA K.; LERUM, RONALD V.; GORMLEY, JOHN
To: GRANT INDUSTRIES, INC.
Reel/Frame 067304/0452 →
Continuity (5)
Continuation 17625964
Provisional Application 63018859 · May 1, 2020
Provisional Application 62872588 · Jul 10, 2019
Provisional Application 62872592 · Jul 10, 2019
Related Publication 20240342061A1 · Oct 17, 2024
References Cited (69)
US 3192185A · Achterhof et al. · 1965 [cited by applicant]
US 3627719A · Sellet · 1971 [cited by applicant]
US 4404296A · Schaepel · 1983 [cited by applicant]
US 4661099A · Von Bittera et al. · 1987 [cited by applicant]
US 5284897A · Columbus et al. · 1994 [cited by applicant]
US 5908631A · Arnaud et al. · 1999 [cited by applicant]
US 7799874B2 · Carr et al. · 2010 [cited by applicant]
US 8222363B2 · Lin et al. · 2012 [cited by applicant]
US 9376404B2 · Nakagawa et al. · 2016 [cited by applicant]
US 9610237B2 · Burgo et al. · 2017 [cited by applicant]
US 10035871B2 · Langer et al. · 2018 [cited by applicant]
US 20030092932A1 · Tong et al. · 2003 [cited by applicant]
US 20050276770A1 · Filippi et al. · 2005 [cited by applicant]
US 20080287604A1 · Wibaux · 2008 [cited by applicant]
US 20090081137A1 · Nguyen et al. · 2009 [cited by applicant]
US 20090232752A1 · Carson et al. · 2009 [cited by applicant]
US 20110014139A1 · Mala et al. · 2011 [cited by applicant]
US 20110045983A1 · Healy et al. · 2011 [cited by applicant]
US 20120046358A1 · Cheng et al. · 2012 [cited by applicant]
US 20120270992A1 · Larock et al. · 2012 [cited by applicant]
US 20130079486A1 · Hidesaki et al. · 2013 [cited by applicant]
US 20130149260A1 · Delvalle et al. · 2013 [cited by applicant]
US 20150128335A1 · Dehni · 2015 [cited by applicant]
US 20150197610A1 · Peterson et al. · 2015 [cited by applicant]
US 20160067153A1 · Chen et al. · 2016 [cited by applicant]
US 20180079852A1 · Hecking et al. · 2018 [cited by applicant]
US 20180208720A1 · Hasegawa et al. · 2018 [cited by applicant]
US 20180311140A1 · Perner et al. · 2018 [cited by applicant]
US 20180369125A1 · Woodland et al. · 2018 [cited by applicant]
US 20180371149A1 · Langer et al. · 2018 [cited by applicant]
US 20190169390A1 · Peterson et al. · 2019 [cited by applicant]
EP 1142959A1 · 2001 [cited by applicant]
EP 2365024A1 · 2011 [cited by applicant]
EP 2380557A1 · 2011 [cited by applicant]
EP 2759572A1 · 2014 [cited by applicant]
EP 3778689A1 · 2021 [cited by applicant]
EP 3778690A1 · 2021 [cited by applicant]
JP H04320457A · 1992 [cited by applicant]
JP H05262622A · 1993 [cited by applicant]
JP 2000313731A · 2000 [cited by applicant]
JP 3631542B2 · 2005 [cited by applicant]
JP 2008201698A · 2008 [cited by applicant]
JP 2008239542A · 2008 [cited by applicant]
JP 2008260722A · 2008 [cited by applicant]
JP 2011178693A · 2011 [cited by applicant]
JP 2017114773A · 2017 [cited by applicant]
JP 2018090662A · 2018 [cited by applicant]
JP 2018199653A · 2018 [cited by applicant]
JP 6892253B2 · 2021 [cited by applicant]
WO 2008039466A1 · 2008 [cited by applicant]
WO 2013074655A1 · 2013 [cited by applicant]
WO 2014167518A1 · 2014 [cited by applicant]
WO 2016090081A1 · 2016 [cited by applicant]
WO 2018122532A1 · 2018 [cited by applicant]
WO 2018183440A1 · 2018 [cited by applicant]
WO 2021007489A1 · 2021 [cited by applicant]
WO 2021231527A1 · 2021 [cited by applicant]
WO 2021257937A1 · 2021 [cited by applicant]
Extended European Search Report for Corresponding European Application No. 20855942.7, Nov. 8, 2023, 13 Pages. [cited by applicant]
Aguilar-Castro et al., “Biobased polyester obtained from bifunctional monomers through metathesis of fatty acids as precursor to synthesis of polyurethanes.” J. Appl. Polym. Sci., 136: 47095 (2018). [cited by applicant]
Mutlu et al., “Castor oil as a renewable resource for the chemical industry.” Eur. J. Lipid Sci. Technol., 112: 10-30 (2010). [cited by applicant]
Srivastava et al., “Gel Point Prediction of Metal-filled Castor Oil-based Polyurethanes System.” Polym. Adv. Technol., 13: 1055-1066 (2002). [cited by applicant]
International Search Report issued in International Application No. PCT/US2020/041540, mailed Oct. 16, 2020. [cited by applicant]
Jones, Charla, What Is Coco-Caprylate Doing In My Natural Skin Care Products? Eu2Be (May 8, 2015): pp. 1-2 <https://eu2be.com/blogs/discover/19389252-what-is-coco-caprylate-doing-in-my-natural-skin-care-producls>; p. 2. [cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2020/046170 (10 Pages) (Nov. 18, 2020). [cited by applicant]
International Preliminary Report on Patentability for International Application No. PCT/US2020/046170 (9 Pages) (Mar. 10, 2022). [cited by applicant]
Written Opinion corresponding to PCT/US2020/041540 (14 Pages) (Oct. 16, 2020). [cited by applicant]
Becker et al., “Safety Assessment of Polyurethanes as Used in Cosmetics,”, Cosmetic Ingredient Review, pp. 1-96., 2017. [cited by applicant]
Hamid Yeganeh, et al., “Preparation and properties of novel biodegradable polyurethane networks based on castor oil and poly(ethylene glycol)” Polymer Degradation and Stability, vol. 92, pp. 480-489, 2007. [cited by applicant]