IP Library Granted Patent US 12,389,934
Granted Patent B2
US 12,389,934 · App. 17/845,341 · Granted Aug 19, 2025

Organic-based nicotine gel compositions

Inventors: Samira Bagheri (Mountain View, CA); Namhey Lee (Hayward, CA); Anusha Saripalli (Santa Clara, CA); Krishnamohan Sharma (Milpitas, CA)
Assignee: JUUL Labs, Inc.
A24B15/243A24B15/165B01J13/0052C08J3/245A24F40/42
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 12,389,934
App. No.
17/845,341
Granted
Aug 19, 2025
Kind
B2
Abstract

Compositions include an aqueous organic-based gellant system and nicotine or a salt thereof. The compositions are readily prepared and stored in cartridges or used directly in a device for delivering nicotine to a user.

Claims (30)

1. A composition comprising:

an aqueous polysaccharide-based gellant system comprising:

a polysaccharide gel matrix comprising:

a polysaccharide; and

a gel modifier comprising a crosslinker, wherein the crosslinker comprises a borate, a titanate, a calcium ion, an aluminum ion, a copper ion, a zinc ion, a zirconium ion, a magnesium ion, or combinations thereof; and

a water-soluble polymer, wherein the water-soluble polymer is selected from the group consisting of a poloxamer, a polyether, a polyvinylpyrrolidone, a polyvinyl alcohol, a polyacrylamide, a polyoxazoline, a polyphosphate, an albumin, and combinations thereof; and

nicotine or a salt thereof,

wherein the nicotine or salt thereof is disposed within the polysaccharide gel matrix, and wherein the water-soluble polymer encapsulates the polysaccharide gel matrix.

2. The composition of claim 1 , wherein the water-soluble polymer has a number average molecular weight (Mn) from about 5,000 daltons to about 30,000 daltons.

3. The composition of claim 1 , further comprising a humectant, wherein the humectant comprises propylene glycol, vegetable glycerin, triacetin, sorbitol, xylitol, 1,3-propanediol, or combinations thereof.

4. The composition of claim 3 , wherein the propylene glycol, vegetable glycerin, or combinations thereof comprises less than 50% w/w of the composition.

5. The composition of claim 3 , wherein the propylene glycol, vegetable glycerin, or combinations thereof comprise less than 20% w/w of the composition.

6. The composition of claim 3 , wherein the propylene glycol, vegetable glycerin, or combinations thereof comprise less than 10% w/w of the composition.

7. The composition of claim 3 , wherein the propylene glycol, vegetable glycerin, or combinations thereof comprise less than 1% w/w of the composition.

8. The composition of claim 1 , wherein the polysaccharide is selected from the group consisting of an alginic acid, a cellulose, a guar (galactomannan), a xanthan gum, an agar, a gellan, an amylose, a welan gum, a rhamsan, a carrageenan, a chitosan, a scleroglucan, a diutan gum, a pectin, a starch, derivatives thereof, and combinations thereof.

9. The composition of claim 8 , wherein the cellulose is selected from the group consisting of cellulose, methyl cellulose, ethyl cellulose, ethyl methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl methyl cellulose, hydroxypropyl methyl cellulose, ethyl hydroxyl ethyl cellulose, carboxymethyl cellulose, carboxymethylhydroxyethyl cellulose, cellulose sulfate, cellulose acetate, and combinations thereof.

10. The composition of claim 8 , wherein the guar is selected from the group consisting of natural guar, hydroxypropyl guar (HPG), sulfonated guar, sulfonated hydroxypropyl guar, carboxymethyl hydroxypropyl guar (CMHPG), and carboxymethyl guar.

11. The composition of claim 8 , wherein the alginic acid is selected from the group consisting of sodium alginate, ammonium alginate, and potassium alginate.

12. The composition of claim 1 , wherein the crosslinker further comprises a divalent or trivalent metal cation.

13. The composition of claim 12 , wherein crosslinker further comprises an alkaline earth metal.

14. The composition of claim 1 , wherein nicotine or salt thereof is present in an amount from about 1% w/w to about 5% w/w.

15. The composition of claim 1 , wherein the gellant system is provided in the form of macroscopic beads, a film, a solid mass, or as a plurality of particles.

16. The composition of claim 15 , wherein the macroscopic beads have a diameter from about 100 microns to about 3 mm.

17. The composition of claim 1 , wherein the gellant system reversibly forms a fluid liquid on heating and reforms the gellant system on cooling.

18. The composition of claim 1 , wherein a ratio of the polysaccharide matrix to the water-soluble polymer is about 10:1 to about 1.5:1.

19. The composition of claim 1 , wherein a ratio of the polysaccharide matrix to the water-soluble polymer is about in a range of about 5:1 to about 2:1.

20. A process comprising:

adding nicotine or a salt thereof to a polysaccharide;

adding a gel modifier to the polysaccharide, wherein the gel modifier comprises a crosslinker, wherein the crosslinker comprises a borate, a titanate, a calcium ion, an aluminum ion, a copper ion, a zinc ion, a zirconium ion, a magnesium ion, or combinations thereof, thereby forming a polysaccharide gel matrix having disposed therein the nicotine or salt thereof; and

adding a water-soluble polymer to the polysaccharide gel matrix, wherein the water-soluble polymer is selected from the group consisting of a poloxamer, a polyether, a polyvinylpyrrolidone, a polyvinyl alcohol, a polyacrylamide, a polyoxazoline, a polyphosphate, an albumin, and combinations thereof, and wherein the water-soluble polymer encapsulates the polysaccharide gel matrix, thereby forming an aqueous polysaccharide-based gellant system.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Oct 17, 2024
From: ALTER DOMUS (US) LLC
To: JUUL LABS, INC.; VMR PRODUCTS LLC; ENVENIO INC.
Reel/Frame 069185/0228 →
SECURITY INTEREST Recorded Jul 11, 2023
From: JUUL LABS, INC.; VMR PRODUCTS LLC; ENVENIO INC.
To: ALTER DOMUS (US) LLC
Reel/Frame 064252/0225 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 062114 FRAME: 0196. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 23, 2022
From: JUUL LABS, INC.
To: JLI NATIONAL SETTLEMENT TRUST
Reel/Frame 062214/0142 →
SECURITY INTEREST Recorded Dec 10, 2022
From: JUUL LABS, INC.
To: JLI NATIONAL SETTLEMENT TRUST
Reel/Frame 062114/0195 →
SECURITY INTEREST Recorded Sep 30, 2022
From: JUUL LABS, INC.
To: ALTER DOMUS (US) LLC
Reel/Frame 061578/0865 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2022
From: BAGHERI, SAMIRA; LEE, NAMHEY; SARIPALLI, ANUSHA; SHARMA, KRISHNAMOHAN
To: JUUL LABS, INC.
Reel/Frame 060318/0943 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2022
From: BAGHERI, SAMIRA; LEE, NAMHEY; SARIPALLI, ANUSHA; SHARMA, KRISHNAMOHAN
To: JUUL LABS, INC.
Reel/Frame 060319/0106 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2022
From: BAGHERI, SAMIRA; LEE, NAMHEY
To: JUUL LABS, INC.
Reel/Frame 060318/0926 →