IP Library › Granted Patent US 11,819,490
Granted Patent B2
US 11,819,490 · App. 16/338,273 · Granted Nov 21, 2023

Dilutable formulations of cannabinoids and processes for their preparation

Inventors: Nissim Garti (Ramat HaSharon, IL); Sharon Garti Levi (Modi'in, IL); Rotem Edri (Eilat, IL)
Assignee: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD.
A61K31/352A61K9/1075A61K9/19A61K9/4841A61K47/10A61K47/14A61K47/24A61K47/26A61K47/32A61K47/44
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 11,819,490
App. No.
16/338,273
Granted
Nov 21, 2023
Kind
B2
Abstract

Cannabinoid-loaded formulations are characterized by including 0.5 wt. % to 20 wt. % medium chain triglycerides, one or more hydrophilic surfactants, one or more co-surfactants and 0.1 wt. % or more of at least one cannabinoid. The formulations are in microemulsion form, and are fully dilutable by an aqueous diluent.

Claims (17)

1. A cannabinoid-loaded formulation, comprising:

at least one oil comprising medium chain triglycerides (MCT), the oil being in an amount of between about 0.5 wt % and 10 wt %,

at least one hydrophilic surfactant in an amount of between about 30 and about 85 wt %, said at least one hydrophilic surfactant is selected from the group consisting of polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monooleate, polyoxyethylene esters of saturated and unsaturated castor oil, ethoxylated monoglycerol esters, ethoxylated fatty acids, and combinations thereof,

at least one co-surfactant in an amount of between about 1 wt % and about 50 wt %, the ratio between the at least one hydrophilic surfactant and the at least one co-surfactant is between about 1:1 and 6:1 (wt/wt), said at least one co-surfactant is selected from the group consisting of polyols, diglycerides, polyglyceryl-3 dioleate, phospholipids, polyoxyethylenes, and combinations thereof,

at least one solvent in an amount of between 0 wt % and 15 wt %, and

at least one cannabinoid in an amount of between about 0.1 wt % and about 12 wt %, said at least one cannabinoid is selected from the group consisting of cannabigerolic acid (CBGA), cannabigerolic acid monomethylether (CBGAM), cannabigerol (CBG), cannabigerol monomethylether (CBGM), cannabigerovarinic acid (CBGVA), cannabigerovarin (CBGV), cannabichromenic acid (CBCA), cannabichromene (CBC), cannabichromevarinic acid (CBCVA), cannabichromevarin (CBCV), cannabidiolic acid (CBDA), cannabidiol (CDB), cannabidiol monomethylether (CBDM), cannabidiol-C 4 (CBD-C 4 ), cannabidivarinic acid (CBDVA), cannabidiorcol (CBD-C 1 ), delta-9-tetrahydrocannabinolic acid A (THCA-A), delta-9-tetrahydrocannabinolic acid B (THCA-B), delta-9-tetrahydrocannabinol (THC), delta-9-tetrahydrocannabinolic acid-C 4 (THCA-C 4 ), delta-9-tetrahydrocannabinol-C 4 (THCA-C 4 ), delta-9-tetrahydrocannabivarinic acid (THCVA), delta-9-tetrahydrocannabivarin (THCV), delta-9-tetrahydrocannabiorcolic acid (THCA-C 1 ), delta-9-tetrahydrocannabiorcol (THC-C 1 ), delta-7-cis-isotetrahydrocannabivarin, delta-8-tetrahydrocannabinolic acid A (Δ 8 -THCA), delta-8-tetrahydrocannabinol (Δ 8 -THC), cannabicyclolic acid (CBLA), cannabicyclol (CBL), cannabicyclovarin (CBLV), cannabielsoic acid A (CBEA-A), cannabielsoic acid B (CBEAB), cannabielsoin (CBE), cannabinolic acid (CBNA), cannabinol (CBN), cannabinol methylether (CBNM), cannabinol-C 4 (CBN-C 4 ), cannabivarin (CBV), cannabinol-C 2 (CBNC2), cannabiorcol (CBN-C 1 ), cannabinodiol (CBND), cannabinodivarin (CBVD), cannabitriol (CBT), 10-ethoxy-9-hydroxy-delta-6a-tetrahydrocannabinol, 8,9-dihydroxy-delta-6a-tetrahydrocannabinol, cannabitriolvarin (CBTV), ethoxy-cannabitriolvarin (CBTVE), dehydrocannabifuran (DCBF), cannabifuran (CBF), cannabichromanon (CBCN), cannabicitran (CBT), 10-oxo-delta-6a-tetrahydrocannabinol (OTHC), delta-9-cistetrahydrocannabinol (cis-THC), 3,4,5,6-tetrahtdro-7-hydroxy-α-α-2-trimethyl-9-n-propyl-2,6-methano-2H-1-benzoxocin-5-methanol (OH-iso-HHCV), cannabiripsol (CBR), trihydroxy-delta-9-tetrahydroxycannabinol (triOH-THC), and any combination thereof;

the formulation being in form of a water-free microemulsion having a droplet size of between about 5 nm and about 100 nm, and being fully dilutable by an aqueous diluent.

2. The cannabinoid-loaded formulation of claim 1 , further comprising at least one additional oil, different from MCI, the at least one additional oil is selected from the group consisting of mineral oil, paraffinic oils, vegetable oils, glycerides, esters of fatty acids, liquid hydrocarbons and mixtures thereof.

3. The cannabinoid-loaded formulation of claim 2 , wherein said at least one additional oil is selected from the group consisting of olive oil, soybean oil, canola oil, cotton oil, palmolein, sunflower oil, corn oil, rapeseed oil, grape seeds oil, hemp oil, pomegranate oil, avocado oil, peppermint oil, tomato oil, isopropyl myristate, oleyl lactate, coca caprylocaprate, hexyl laurate, oleyl amine, oleic acid, oleyl alcohol, linoleic acid, linoleyl alcohol, ethyl oleate, hexane, heptanes, nonane, decane, dodecane, D-limonene, neem oil, lavender oil, anise oil, rosemary oil, sage oil, hibiscus oil, menthol, capsaicin, grape seed oil, pumpkin oil, hemp oil, triglycerides or esters of fatty acids and mixtures thereof.

4. The cannabinoid-loaded formulation of claim 1 , having a droplet size of between about 5 and about 30 nanometers.

5. The cannabinoid-loaded formulation of claim 1 , wherein the formulation is capable of stabilizing the at least one cannabinoid in acidic environments.

6. The cannabinoid-loaded formulation of claim 5 , wherein the acidic environment is gastric fluid.

7. The cannabinoid-loaded formulation of claim 6 , wherein the at least one cannabinoid is cannabidiol (CBD), and wherein the formulation reduces the rate of transformation of the CBD into tetrahydrocannabinol (THC).

8. A pharmaceutical composition comprising the cannabinoid loaded-formulation of claim 1 .

9. The pharmaceutical composition of claim 8 , being in a form selected from a gel, a lotion, oil, soap, a spray, an emulsion, a cream, an ointment, capsules, soft-gel capsules, a patch, or a solution.

10. The pharmaceutical composition of claim 8 , adapted for delivery of said cannabinoid topically, orally, by inhalation, nasally, transdermally, occularly or parenterally into the circulatory system of a subject.

11. The pharmaceutical composition of claim 8 , further comprising a pharmaceutically acceptable carrier and/or a diluent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2019
From: GARTI, NISSIM; GARTI LEVI, SHARON; EDRI, ROTEM
To: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD.
Reel/Frame 048883/0664 →
Priority Claims (1)
IL 248149 · Sep 29, 2016 · national
Continuity (1)
Related Publication 20190314326A1 · Oct 17, 2019