IP Library Granted Patent US 12,508,221
Granted Patent B2
US 12,508,221 · App. 17/469,012 · Granted Dec 30, 2025

Topical compositions and methods of use

Inventors: Venkat R. Goskonda (Phoenix, AZ); Ravi Nallakrishnan (Willowbrook, IL)
Assignee: PS Therapy Ltd
A61K9/0014A61K9/06A61K31/167A61K47/10A61K47/44
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 12,508,221
App. No.
17/469,012
Granted
Dec 30, 2025
Kind
B2
Abstract

The present invention is directed to a topical composition comprising one or more active ingredients and one or more permeation enhancers. The present invention is further directed to a method of reducing or eliminating one or more conditions selected from the group consisting of pain, hemorrhoids, acne, wrinkles and scars.

Claims (28)

1 . A topical composition comprising lidocaine or a salt thereof, one or more nonionic surfactants, one or more viscosity enhancers, a mixture of propylene glycol monolaurate and propylene glycol at a ratio of about 1:9 and ethanol.

2 . The composition of claim 1 , wherein the one or more nonionic surfactants are selected from the group consisting of poloxamers, polysorbates, cyclodextrins, alkylaryl polyethers, polyoxyethyleneglycol alkyl ethers, tyloxapol, and polyoxyls.

3 . The composition of claim 2 , wherein the one or more nonionic surfactants are selected from the group consisting of poloxamer 188, poloxamer 407, polysorbate 20, polysorbate 60, polysorbate 80, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan monooleate, 2-HP-cyclodextrin, sulfobutylether β-cyclodextrin, hydroxypropyl-gamma-cyclodextrin, polyoxyl 40 stearate, polyoxyl 30 castor oil, polyoxyl 35 castor oil, polyoxyl 40 hydrogenated castor oil and polyoxyethylene glycol alkyl ethers.

4 . The composition of claim 3 , wherein the one or more nonionic surfactants are selected from the group consisting of poloxamer 407, poloxamer 188 and polyoxyl 35 castor oil.

5 . The composition of claim 1 , wherein the one or more viscosity enhancers are selected from the group consisting of cellulose derivatives, gums, dextrans, polyvinyl alcohol, polyacrylic acids, povidone, polyethylene glycol, propylene glycol, chitosans, and hyaluronates and hyaluronic acids.

6 . The composition of claim 5 , wherein the one or more viscosity enhancers are selected from the group consisting of cellulose derivatives and polyacrylic acids.

7 . The composition of claim 6 , wherein the one or more viscosity enhancers are selected from the group consisting of sodium carboxymethyl cellulose and carbomer 974P.

8 . The composition of claim 1 , further comprising one or more excipients selected from the group consisting of co-solvents and cooling agents.

9 . The composition of claim 8 , wherein the one or more excipients are selected from the group consisting of polyethylene glycol 400, menthol and isopropyl alcohol.

10 . A method of reducing or eliminating one or more conditions selected from the group consisting of pain, hemorrhoids, acne, wrinkles and scars comprising topically applying an effective amount of a composition of claim 1 to a subject in need thereof.

11 . A method of treating gastrointestinal conditions or diseases comprising applying a composition of claim 1 to a subject in need thereof.

12 . A topical analgesic composition comprising lidocaine or a salt thereof and a mixture of propylene glycol monolaurate and propylene glycol at a ratio of about 1:9, and ethanol.

13 . The composition of claim 12 , further comprising one or more surfactants and one or more viscosity enhancers.

14 . The composition of claim 13 , wherein the one or more nonionic surfactants are selected from the group consisting of poloxamer 407, poloxamer 188 and polyoxyl 35 castor oil.

15 . The composition of claim 13 , wherein lidocaine or a salt thereof is at a concentration from about 2% to about 4% w/w, the one or more nonionic surfactants are at a total concentration from about 1% to about 2% w/w, the one or more viscosity enhancers are at a concentration from about 0.5% to about 2% w/w and the mixture of propylene glycol monolaurate and propylene glycol at ratio of about 1:9 is at a concentration from about 2% to about 5% w/w.

16 . A method of reducing or eliminating pain, hemorrhoids or a combination thereof comprising topically applying an effective amount of a composition of claim 12 to a subject in need thereof.

17 . A method of treating gastrointestinal conditions or diseases comprising applying a composition of claim 12 to a subject in need thereof.

18 . A topical analgesic composition comprising:

about 4.0% w/w lidocaine;

about 1.0% w/w poloxamer 407;

about 0.2% w/w poloxamer 188;

about 0.25% w/w polyoxyl 35 castor oil;

about 3.0% w/w of a mixture of propylene glycol monolaurate and propylene glycol at a ratio of about 1:9; and

about 1.0% w/w carbomer 974P, and about 5.0% w/w ethanol.

19 . The composition of claim 18 , further comprising;

about 5% w/w isopropyl alcohol;

about 0.75% w/w menthol; and

about 0.5% w/w polyethylene glycol 400.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 25, 2024
From: GOSKONDA, VENKAT R; NALLAKRISHNAN, RAVI
To: PST THERAPY LTD.
Reel/Frame 069399/0587 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2022
From: PS THERAPY LTD.
To: PS THERAPY, INC.
Reel/Frame 060087/0448 →
Continuity (3)
Provisional Application 63077255 · Sep 11, 2020
Provisional Application 63090369 · Oct 12, 2020
Related Publication 20220079873A1 · Mar 17, 2022
References Cited (8)
US 5358715A · Wong · 1994 [cited by examiner]
US 20060153905A1 · Carrara · 2006 [cited by examiner]
US 20100292199A1 · Leverd · 2010 [cited by examiner]
US 20190262290A1 · Horn · 2019 [cited by examiner]
Chessa et al (Effect of Penetration Enhancer Containing Vesicles on the Percutaneous Delivery of Quercetin through New Born Pig Skin. Pharmaceutics 2011, 3, 497-509) (Year: 2011). [cited by examiner]
Naik et al (Mechanism of oleic acid-induced skin penetration enhancement in vivo in humans. Journal of Controlled Release 37 (1995) 299-306) (Year: 1995). [cited by examiner]
Kouchak et al (Effects of Various Penetration Enhancers on Penetration of Aminophylline Through Shed Snake Skin. Jundishapur J Nat Pharm Prod. Feb. 2014; 9(1): 24-9) (Year: 2014). [cited by examiner]
Karami et al (On iontophoretic delivery enhancement: Ionization and mobility of lidocaine hydrochloride in propylene glycol. International Journal of Pharmaceutics 168 (1998) 85-95) (Year: 1998). [cited by examiner]