CA2503310A1 - Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking - Google Patents

Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking Download PDF

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Publication number
CA2503310A1
CA2503310A1 CA002503310A CA2503310A CA2503310A1 CA 2503310 A1 CA2503310 A1 CA 2503310A1 CA 002503310 A CA002503310 A CA 002503310A CA 2503310 A CA2503310 A CA 2503310A CA 2503310 A1 CA2503310 A1 CA 2503310A1
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CA
Canada
Prior art keywords
thc
cannabis
decarboxylation
flowers
conversion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002503310A
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French (fr)
Inventor
Antony Paul Hornby
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CA002503310A priority Critical patent/CA2503310A1/en
Publication of CA2503310A1 publication Critical patent/CA2503310A1/en
Abandoned legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)

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  • Health & Medical Sciences (AREA)
  • Natural Medicines & Medicinal Plants (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Medical Informatics (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Pyrane Compounds (AREA)
  • Alternative & Traditional Medicine (AREA)

Abstract

A method is described whereby the latent cannabinoids in the cannabis plant (sativa or indiga) can be activated to make them more efficacious as an orally administered medicine or for sublingual, suppository or patch applications. The process described is primarily a decarboxylation of the acid form of a number of cannabinoid molecules to the alcohol moiety. This decarboxylation step is performed by heating the ground cannabis leaves and flowers for a specific time- period and temperature in a custom designed container. The decarboxylation of Tetrahydrocannabinolic Acid (THC-A) to Delta-9 Tetrohydrocannabinol (THC) transforms the THC-A from a compound with no known physiological activity to THC with very well characterized immune, anti-inflammatory and psycho-activity. Similarly, the decarboxylation of cannabidiolic acid to cannabidiol activates these molecules that, in turn, is thought to modulate the effects of THC. These activated compounds are now useful for making standardized dosages of cannabis medicine. The resultant preparations from this process can be used in either oral, sublingual, suppository or patch administrations.

Description

Background to the Invention:
Patent No. ZA200306794 speaks of an invention that ultilises organic solvents to prepare extracts from cannabis. This patent uses no organic solvent or extraction procedure in its formulation.
Patent No. W02004016277 teaches an extraction method using super critical fluid extraction of cannabinoids from plant material the method described here uses no fluid extraction procedure and does not substitute with synthetic analogues if extracted material is not available.

Patent No. US2003191180 speaks again of organic solvent extraction of cannabinoids from plant material plus the use of the invention for synthetic analogues. The patent described here references only natural product material and no organic solvent is required for extraction.
Patent No. W003063847 teaches an anti-nausea formulation based on solvent extraction of THC-A. In the patent described here no extraction proceeds activation of THC-A
to THC.
Patent No. US2002086438 again teaches an organic solvent extraction of cannabinoids to be used in medicinal formulations. This patent describes the use of no organic solvent and any stage in the preparation of the product.
Cannabis (Sativa and Indiga) has been used for many thousands of years as medicine to treat a multitude of ailments from arthritis to multiple sclerosis. For the most part the administrative route has been in the smoked form. By burning the dried cannabis leaves and flowers the medicinal compounds within the plant matrix become activated and hence elicit their physiological effects. If the cannabis is not heated as in smoking or baking into brownies, the THC is not activated and the medicinal properties of the cannabinoids do not present.
Heating of cannabis to activate the major cannbinoid constituents must be done within a rather narrow temperature window. Not heating the cannabis enough will allow only partial conversion of the acids to the alcohols, heating too much will cause conversion and subsequent loss of the converted cannabinoids to atmosphere through vaporization.
With the invention described here, one can take a known weight of cannabis plant, place it in a special container, heat the container and cannabis for a set time at a specified temperature and accomplish the same degree of conversion each time.
This reproducible conversion method allows the creation of standardized cannabis medicine, with known dosages, that can be used for oral applications.
The standardization of cannabis medicine for oral administration requires two analytical steps. One must determine the concentration of the THC-A in the starting raw material before grinding and conversion. This pre-determination of THC-A allows for better adjustment of the subsequent heating temperature to be applied to the preparation.
More importantly, identification and quantification of the individual cannabinoids in the post-heating mixture is not only vital to the standardization process, but is also required to note the percentage conversion of THC-A to THC. If conversion is not complete, temperature can be reapplied until conversion optimized per unit time. If however, the sample has been over-heated then the THC concentration in the finished product will be lower because of burn-off and cannot be recovered.
The design of the container for holding the cannabis during heating is also paramount to the efficiency of conversion. Optimally, conversion should mean the removal of carbon dioxide from the acidic cannabinoids and little else. Since the heating process will vaporize other low molecular weight and boiling point compounds that may also be therapeutic, loss of these compounds is to be avoided. As stated previously, the optimal conversion removes only C02. 'The container design is such that optimum efficiency is achieved.
The THC level of the converted cannabis can also be modulated by this method.
That is an exact concentration of THC can be achieved in each preparation, by adjusting the heating time interval. By utitilizing, this method the THC to THC-A ratio can be adjusted to any desired level be using specified temperature and time settings. Thus, specific dosages of THC can be achieve within a raw material, making the formulation of standardized products more feasible and cost efficient.
Objectives of the Invention:
1.) An objective of this invention is to allow reproducible conversions of quantifiable amounts of cannabinoid acids in cannabis leaves and flowers to equivalent amounts of their individual alcohols.
2.) A further objective of this invention is to allow activation of specific cannabinoid compounds by a heating/decarboxylation method that allows high yields of the activated cannabinoids.
3.) A further objective is to provide a method whereby formerly non-psycho-active cannabinoids are decarboxylated to their psycho-active moiety and hence become useful in the treatment of symptoms of many ailments.
4.) A further objective is to provide a method whereby the THC content of a therapeutic sample can be modulated to achieve a specific dosage of said active in a standardized formula.
5.) A further objective of this invention is to provide a means of standardizing cannabis medicines with known dosages of active THC per gram of raw material. Since the degree of conversion by the described method can be determined by High Pressure Liquid Chromatography (HPLC) in a raw material preparation a fixed dosage can be made and the product standardized.
6.) A further objective is to allow production of activated standardized raw material for use in oral, sublingual, suppository or patch applications.
7.) A further objective is to produce formulations without the use of organic solvents or supercritical fluids to extract cannabinoids from plant material.

Summary of the Invention:
Described here is a method/process whereby the medicinal compounds contained in cannabis plant material (leaves and flowers) are activated to be useful for administrative routes other than smoking. Such an application also allows for the standardization of the converted material into known dosages of activated THC.

Claims

Claims:

What is claimed:

Claim 1: A process for converting the flowers and leaves of the cannabis plant (flowers and leaves) by specific heating, time and containment protocols yields a product that is amenable to standardization and administrative routes other than smoking.

A method of claim 1 whereby cannabis material (leaves and flowers) is ground to a mesh size that allows for consistent heating.

A method of claim 2 whereby ground cannabis material is heated to a specific temperature to allow conversion (de-carboxylation).

A method of claim 3 whereby heated ground cannabis material is kept at a specific temperature for a specific time to allow optimal conversion of the THC-A to THC.

A method of claim 4 whereby the percentage conversion of the THC-A to THC can be optimized to allow maximum efficiency and efficacy in the finished product.

A method of claim 5 whereby the concentration of converted THC can be determined and thus allow standardization of cannabis in to known dosages of active THC.

A method of claim 6 whereby the standardized cannabis can be used as medicines administered orally, in a sublingual fashion, as a suppository or in a patch.
CA002503310A 2005-04-08 2005-04-08 Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking Abandoned CA2503310A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA002503310A CA2503310A1 (en) 2005-04-08 2005-04-08 Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA002503310A CA2503310A1 (en) 2005-04-08 2005-04-08 Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking

Publications (1)

Publication Number Publication Date
CA2503310A1 true CA2503310A1 (en) 2006-10-08

Family

ID=37101404

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002503310A Abandoned CA2503310A1 (en) 2005-04-08 2005-04-08 Method of activation of cannabis to render standardized preparations for therapeutic administration, other than smoking

Country Status (1)

Country Link
CA (1) CA2503310A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015069763A3 (en) * 2013-11-05 2015-10-08 First Watersign Llc Sublingual cannabis dosage form and methods of making and using the same
US20150352044A1 (en) * 2014-06-06 2015-12-10 CannTrust Inc. Single serve beverage pod containing cannabis
WO2016064987A1 (en) * 2014-10-21 2016-04-28 United Cannabis Corp. Cannabis extracts and methods of preparing and using same
IT201800010262A1 (en) * 2018-11-12 2020-05-12 Kyvaris Pharma Srls Formulation in macro-granules based on therapeutic cannabis and related production method
US12070479B1 (en) 2021-04-19 2024-08-27 PT Worldwide Decarboxylated cannabis compositions and methods of making the same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015069763A3 (en) * 2013-11-05 2015-10-08 First Watersign Llc Sublingual cannabis dosage form and methods of making and using the same
US20150352044A1 (en) * 2014-06-06 2015-12-10 CannTrust Inc. Single serve beverage pod containing cannabis
US9480647B2 (en) * 2014-06-06 2016-11-01 CannTrust Inc. Single serve beverage pod containing cannabis
US10758481B2 (en) 2014-06-06 2020-09-01 CannTrust Inc. Single serve beverage pod containing cannabis
US11628142B2 (en) 2014-06-06 2023-04-18 CannTrust Inc. Single serve beverage pod containing cannabis
WO2016064987A1 (en) * 2014-10-21 2016-04-28 United Cannabis Corp. Cannabis extracts and methods of preparing and using same
US9730911B2 (en) 2014-10-21 2017-08-15 United Cannabis Corp. Cannabis extracts and methods of preparing and using same
US10555928B2 (en) 2014-10-21 2020-02-11 United Cannabis Corp. Cannabis extracts and methods of preparing and using same
US11291650B2 (en) 2014-10-21 2022-04-05 United Cannabis Corp. Cannabis extracts and methods of preparing and using same
IT201800010262A1 (en) * 2018-11-12 2020-05-12 Kyvaris Pharma Srls Formulation in macro-granules based on therapeutic cannabis and related production method
US12070479B1 (en) 2021-04-19 2024-08-27 PT Worldwide Decarboxylated cannabis compositions and methods of making the same

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Legal Events

Date Code Title Description
FZDE Discontinued
FZDE Discontinued

Effective date: 20071024