IP Library Patent Application 14271071
Patent Application
App. No. 14/271,071

NICOTINE SALT FORMULATIONS FOR AEROSOL DEVICES AND METHODS THEREOF

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 None
App. No.
14/271,071
Abstract

A nicotine salt liquid formulation for generating an inhalable aerosol in an electronic cigarette comprising nicotine salt that forms about 0.5% to about 20% nicotine is provided.

Claims (42)

1 - 104 . (canceled)

105 . A method of delivering nicotine to a user comprising

(a) deploying an electronic cigarette wherein the electronic cigarette comprises a nicotine salt formulation comprising a nicotine salt in a biologically acceptable liquid carrier wherein an acid used to form said nicotine salt is characterized by a vapor pressure great than or equal to 20 mmHg at 200° C., and

(b) delivering an inhalable aerosol generated from the nicotine salt formulation heated by the electronic cigarette.

106 . The method of claim 105 , wherein the acid comprises a melting point at least 40° C. lower than the operating temperature of the electronic cigarette, and at least a 50° C. difference between a melting point of the acid and a boiling point of the acid.

107 . The method of claim 105 , wherein the operating temperature is from 150° C. to 250° C., or is about 200° C.

108 . The method of claim 105 , wherein the aerosol comprises any combination of condensate of the nicotine salt, condensate of freebase nicotine, condensate of the carrier, and/or condensate of the acid.

109 . The method of claim 105 , wherein the aerosol comprises condensate in particles sizes from about 0.1 microns to about 5 microns, or about 0.3 microns to about 0.4 microns.

110 . The method of claim 105 , wherein the acid is:

a carboxylic acid, or

an organic acid chosen from the group of monocarboxylic acid, aromatic acid, keto acid, formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, capric acid, citric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, phenylacetic acid, benzoic acid, pyruvic acid, levulinic acid, tartaric acid, lactic acid, malonic acid, succinic acid, fumaric acid, finnaric acid, gluconic acid, saccharic acid, salicyclic acid, sorbic acid, malonica acid, or malic acid.

111 . The method of claim 105 , wherein said nicotine salt comprises nicotine pyruvate, nicotine salicylate, nicotine sorbate, nicotine laurate, nicotine levulinate, or nicotine benzoate.

112 . The method of claim 105 , wherein the liquid carrier comprises 20%-50% of propylene glycol and 80% to 50% of vegetable glycerin.

113 . The method of claim 105 , wherein the nicotine salt is in an amount that forms about 0.5% to about 20% nicotine in the inhalable aerosol.

114 . The method of claim 105 , wherein the liquid formulation has a nicotine concentration between about 1% (w/w) to about 25% (w/w).

115 . A method of delivering nicotine to a user comprising

(a) deploying an electronic cigarette wherein the electronic cigarette comprises a nicotine salt formulation comprising a nicotine salt in a biologically acceptable liquid carrier wherein an acid used to form said nicotine salt is further characterized by a melting point at least 40° C. lower than the operating temperature of the electronic cigarette, and at least a 50° C. difference between a melting point of the acid and a boiling point of the acid, and

(b) delivering an inhalable aerosol generated from the nicotine salt formulation heated by the electronic cigarette.

116 . The method of claim 115 , wherein the operating temperature is from 150° C. to 250° C., or is about 200° C.

117 . The method of claim 115 , wherein the aerosol comprises condensate in particles sizes from about 0.1 microns to about 5 microns, or about 0.3 microns to about 0.4 microns.

118 . The method of claim 115 , wherein the acid is:

a carboxylic acid, or

an organic acid chosen from the group of monocarboxylic acid, aromatic acid, keto acid, formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, capric acid, citric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, phenylacetic acid, benzoic acid, pyruvic acid, levulinic acid, tartaric acid, lactic acid, malonic acid, succinic acid, fumaric acid, finnaric acid, gluconic acid, saccharic acid, salicyclic acid, sorbic acid, malonica acid, or malic acid.

119 . The method of claim 115 , wherein said nicotine salt comprises nicotine pyruvate, nicotine salicylate, nicotine sorbate, nicotine laurate, nicotine levulinate, or nicotine benzoate.

120 . The method of claim 115 , wherein the liquid carrier comprises 20%-50% of propylene glycol and 80% to 50% of vegetable glycerin.

121 . The method of claim 115 , wherein the nicotine salt is in an amount that forms about 0.5% to about 20% nicotine in the inhalable aerosol.

122 . The method of claim 115 , wherein the liquid formulation has a nicotine concentration between about 1% (w/w) to about 25% (w/w).

123 . A nicotine salt liquid formulation in an electronic cigarette for generating an inhalable aerosol up on heating in the electronic cigarette, the formulation in the cigarette comprising a nicotine salt in a biologically acceptable liquid carrier wherein an acid used to form said nicotine salt is characterized by vapor pressure of about 20 mmHg to 200 mmHg at 200° C.

124 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the acid comprises a melting point at least 40° C. lower than the operating temperature of the electronic cigarette, and at least a 50° C. difference between a melting point of the acid and a boiling point of the acid.

125 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the electronic cigarette heats the nicotine salt formulation to an operating temperature from 150° C. to 250° C., or about 200° C.

126 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the acid is carboxylic acid or is an organic acid, wherein the organic acid is chosen from the group of monocarboxylic acid, aromatic acid, keto acid, formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, capric acid, citric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, phenylacetic acid, benzoic acid, pyruvic acid, levulinic acid, tartaric acid, lactic acid, malonic acid, succinic acid, fumaric acid, finnaric acid, gluconic acid, saccharic acid, salicyclic acid, sorbic acid, malonica acid, or malic acid.

127 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein said nicotine salt comprises nicotine pyruvate, nicotine salicylate, nicotine sorbate, nicotine laurate, nicotine levulinate, or nicotine benzoate.

128 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the liquid carrier comprises 20%-50% of propylene glycol and 80% to 50% of vegetable glycerin.

129 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the nicotine salt is in an amount that forms about 0.5% to about 20% nicotine in the inhalable aerosol.

130 . The nicotine salt liquid formulation in the electronic cigarette of claim 123 , wherein the liquid formulation has a nicotine concentration between about 1% (w/w) to about 25% (w/w).

131 . A nicotine salt liquid formulation in an electronic cigarette for generating an inhalable aerosol up on heating in the electronic cigarette, the formulation in the cigarette comprising a nicotine salt in a biologically acceptable liquid carrier wherein an acid used to form said nicotine salt is further characterized by a melting point at least 40° C. lower than the operating temperature of the electronic cigarette, and at least a 50° C. difference between a melting point of the acid and a boiling point of the acid.

132 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein the electronic cigarette heats the nicotine salt formulation to an operating temperature from 150° C. to 250° C., or about 200° C.

133 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein the acid is carboxylic acid or is an organic acid, wherein the organic acid is chosen from the group of monocarboxylic acid, aromatic acid, keto acid, formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, capric acid, citric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, phenylacetic acid, benzoic acid, pyruvic acid, levulinic acid, tartaric acid, lactic acid, malonic acid, succinic acid, fumaric acid, finnaric acid, gluconic acid, saccharic acid, salicyclic acid, sorbic acid, malonica acid, or malic acid.

134 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein said nicotine salt comprises nicotine pyruvate, nicotine salicylate, nicotine sorbate, nicotine laurate, nicotine levulinate, or nicotine benzoate.

135 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein the liquid carrier comprises 20%-50% of propylene glycol and 80% to 50% of vegetable glycerin.

136 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein the nicotine salt is in an amount that forms about 0.5% to about 20% nicotine in the inhalable aerosol.

137 . The nicotine salt liquid formulation in the electronic cigarette of claim 131 , wherein the liquid formulation has a nicotine concentration between about 1% (w/w) to about 25% (w/w).

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR EXECUTION DATE PREVIOUSLY RECORDED AT REEL: 043544 FRAME: 0004. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Aug 6, 2018
From: PAX LABS, INC.
To: JUUL LABS, INC.
Reel/Frame 046732/0847 →
CHANGE OF NAME Recorded Aug 14, 2017
From: PAX LABS, INC.
To: JUUL LABS, INC.
Reel/Frame 043544/0004 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2015
From: PLOOM, INC.
To: PAX LABS, INC.
Reel/Frame 035121/0328 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2014
From: BOWEN, ADAM; XING, CHENYUE
To: PLOOM, INC.
Reel/Frame 033367/0718 →