Medicinal Acidic Cannabinoids

Abstract

The invention relates to an acidic cannabinoid for medical use and to a cannabis extract comprising an acidic cannabinoid. The extract may comprise one or more compounds selected from the group consisting of cannabidiolic acid (CBD-A), cannabidiol (CBD), cannabigerolic acid (CBGA), cannabigerol (CBG), cannabinolic acid (CBN-A) and cannabinol. The invention further relates to a method for preparing a preparation comprising extracting an acidic cannabinoid from cannabis.

Description

RELATED APPLICATION(S)[0001]This application is a continuation of Ser. No. 11 / 461,818 and filed Aug. 2, 2006 which is a continuation of PCT application no. PCT / NL2005 / 000075, designating the United States and filed Feb. 2, 2005; which claims the benefit of the filing date of European application no. EP 04075300.6, filed Feb. 2, 2004; all of which are hereby incorporated herein by reference in their entirety.FIELD OF THE INVENTION[0002]The invention relates to an acidic cannabinoid for medical use and to a cannabis extract comprising an acidic cannabinoid.BACKGROUND OF THE INVENTION[0003]Δ9-Tetrahydrocannabinol (THC) is naturally found in cannabis. THC has been reported to have use as an analgesic, for instance for patients suffering from rheumatoid arthritis. A side effect of THC is its psychoactive activity. Further, conventionally THC is administered by smoking, which may be detrimental to general health, in particular to the lungs and the coronary system.[0004]WO 89 / 01332 describ...

AI Technical Summary

Benefits of technology

[0027]It is however an advantage of the invention that an acidic cannabinoid—in particular a compound wherein the first alkyl at the aromatic ring is n-pentyl (such as Z in formula Ia or Ib, or in the equivalent position in an acidic precursor of THC in general)—may be derived from a natural source, such as cannabis. An acidic cannabinoid can be used (to treat a medical indication) directly without further chemical modifications, such as decarboxylising the compound into THC and subsequently metabolising the THC.

[0028]A compound according to the invention may be used in isolated form or in an extract from a natural source, in particular from flower tops of cannabis. Particular suitable is a plant or a part thereof, comprising at least 5 wt. % of acidic cannabinoids, e.g. 5-15 wt. %. Very good results have been achieved with Cannabis sativa, Cannabis indica. Suitable methods to extract an acidic compound according to the invention are known in the art and include liquid extraction, e.g. with an apolar phase, such as chloroform and a polar phase, in particular an aliphatic alcohol, such as methanol or ethanol. In such an extraction the acidic cannabinoid typically is found in the apolar phase, especially if the extraction procedure is carried out at pH lower than 7. The skilled person will know how to carry out a suitable extraction and further process the acidic cannabinoid, based on common general knowledge and the information disclosed herein. It has been found that an extract according to the invention, comprising an acidic cannabinoid is effective in reducing TNF-α excretion in human macrophages, demonstrating an inhibitory effect of the acidic cannabinoid. In an embodiment, it has further surprisingly been found to be effective in increasing interleukin release too (see Examples).

[0029]The preparation of the extract in accordance with the invention is generally carried out under essentially non-decarboxylising conditions to avoid an excessive formation of THC, which may be undesired for its psycho-active side effects and / or for legal reasons, THC at present being illicit in many states. In practice, it is therefore preferred to perform the extraction at a temperature not exceeding 95° C., more preferably at a temperature of less then about 50° C., even more preferably of less than about 25° C. Very good results have been achieved with extraction at a temperature not exceeding about 4° C. The lower limit for the temperature is not particularly critical, as long as the extraction medium remains fluid.

[0030]The extract may then be further processed in any way, without excessive exposure to heat to maintain essentially non-decarboxylising conditions and thus avoid excessive formation of THC. In particular such conditions are met if the extract is not excessively exposed to temperatures of about 200° C. or more. Preferably the extract is processed at a temperature not exceeding about 50° C. More preferably any further processing of the extract takes place at a temperature of about 25° C. or less. Accordingly, the solvent of the extract is preferably removed by lyophilisation.

[0031]In practice, conditions are considered to be essentially non-decarboxylising heat treatment is considered to be non-excessive when the amount of THC as a percentage of the total dry weight of the extract is less than 5 wt. %, preferably less than 2 wt. %, even more preferably less than 0.5 wt. %. For practical reasons the amount of THC is preferably less than the maximum allowable amount to allow use as a non-prescription medicament, as determined by law. In this respect it is interesting to note that the present invention allows for the preparation of extracts with less than about 0.15 wt. % as a percentage of the dry weight without a need for selective removal of THC from the extract.

[0032]THC may be totally absent (i.e. non-determinable by a conventional analytical technique) in an extract or other composition according to the invention. For practical reasons some THC may be present, such as about 0.01 wt. % as a percentage of the dry weight or more.

Problems solved by technology

Further, conventionally THC is administered by smoking, which may be detrimental to general health, in particular to the lungs and the coronary system.

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