ADEMETIONINE AND CANNABIDIOL BASED SOLID PHARMACEUTICAL COMPOSITION AND METHOD FOR PREPARING IT

Abstract

A solid pharmaceutical composition, with no narcotic action, for the oral administration of ademetionine and cannabidiol, to the method for preparing it, and to the pharmaceutical, nutraceutical or veterinary formulations containing it.

Claims

1-13. (canceled)

14. A pharmaceutical composition for oral use, comprising: ademetionine and cannabidiol and at least one pharmaceutically acceptable fatty matter.

15. The composition of claim 14, wherein said fatty matter has a melting point equal to or higher than +30° C.

16. The composition according to claim 15, wherein said fatty matter is chosen from a mono-, di-, tri-glyceride of a fatty acid, a polyether, or mixtures thereof.

17. The composition of claim 14, wherein ademetionine is present in an amount between 20% and 50% of the total weight of the composition, cannabidiol is present in an amount between 1% and 20% of the total weight of the composition, and the fatty matter is less than or equal to 35% of the total weight of the composition.

18. The composition according to claim 14, wherein the ratio of ademetionine to cannabidiol by weight is between 25:1 and 1:1.

19. The composition according to claim 14, further comprising a tetrahydrocannabinol content of less than 0.5% of the total weight of the composition.

20. The composition according to claim 14, further comprising at least one pharmaceutically acceptable emulsifier.

21. The composition according to claim 14, further comprising at least one pharmaceutically acceptable excipient comprising a polyglycol or an ester thereof with a fatty acid.

22. Pharmaceutical formulations in the form of tablets, coated tablets, capsules, stick-packs, containing the composition of claim 14.

23. A method for preparing a pharmaceutical composition, comprising the steps of: a. dosing at least one fatty matter, b. dosing cannabidiol, c. dissolving cannabidiol in the fatty matter, d. dosing ademetionine, and e. mixing ademetionine with the mixture obtained in step c).

24. The method according to claim 22, wherein said ademetionine is mixed with a molten fatty matter.

25. The method according to claim 22, wherein said fatty matter is chosen from a fatty acid or an ester thereof, a mono-, di-, tri-glyceride of a fatty acid, a polyglycol, or mixtures thereof, having a melting point of less than +70° C.

26. Use of the compositions of claim 14 for oral administration of ademetionine and cannabidiol.

Description

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0020] The combination in therapy of ademetionine and CBD in a form of oral administration without narcotic effect could be of great benefit in the treatment of various pathologies, particularly those related to the nervous system, e.g. in cases of depression, anxiety, sleep disorders. Furthermore, in osteoarticular inflammation it could be useful to associate the long-term therapeutic efficacy of ademetionine with the immediate benefit of CBD in the treatment of the associated pain. Unfortunately, such a formulation has not been developed so far, due to the technical problems described above.

[0021] A solid, stable composition with no narcotic activity, consisting of an ademetionine salt and a solution of cannabidiol in a fat or wax, has now been obtained: this composition overcomes the technical difficulties of preparing the usual pharmaceutical forms such as tablets, capsules and orosoluble granules, while improving the stability of both active substances. It therefore allows the simultaneous administration of ademetionine and cannabidiol in a single pharmaceutical formulation. Furthermore, it allows a good flexibility in dosages, as the two active substances can be formulated in widely variable proportions. Furthermore, it has the additional advantage of being not very hygroscopic.

[0022] In its preferred embodiment, the invention consists of a composition having, as a whole: [0023] ademetionine content, expressed as ademetionine-ion, ranging between 10% and 55% of the total weight; [0024] cannabidiol content between 1% and 40% of the total weight; [0025] wax or fat content less than 30% of the total weight.

[0026] For the purposes of the invention, both purified hemp extracts and pure cannabidiol, obtained by extraction or chemical synthesis, may be used. A high level of purity of cannabidiol preparations is not required, it is sufficient to adjust the quantity of the preparation based on the content of the active substance (cannabidiol), as long as the THC content is lower than the legal limits.

[0027] Advantageously, the composition may also comprise other components such as phospholipids, surfactants, lubricants, sweeteners, flavourings and other pharmaceutically accepted excipients.

[0028] In a preferred embodiment, the composition is presented in solid form as a granulate; in a particularly preferred form, said granulate is characterised by a humidity content of less than 5.0%. In a possible embodiment, said granulate is dosed in stick-packs or in capsules. In a further embodiment of the invention, said granulate is used for the preparation of plain or film-coated tablets.

[0029] In further embodiments, said granulate may contain other active substances: for example unsaturated omega-3/6/9 fatty acids, fat-soluble vitamins such as vitamin A, vitamin E, ascorbyl palmitate, carotenes, or other plant extracts, in particular: chamomile, hawthorn, valerian, St. John's wort, tea.

[0030] In a possible embodiment, the invention consists in the process for obtaining a stable composition of ademetionine and fatty matter. In a further aspect, the invention consists in the process for drying said composition.

[0031] The method of the invention comprises: [0032] a) dosing the fatty matter; [0033] b) dosing cannabidiol, [0034] c) dosing any other active substances and/or excipients; [0035] d) dissolving the compounds dosed under points b) and c) in the fatty matter, possibly heating up to melting; [0036] e) dosing ademetionine; [0037] f) mixing ademetionine with the mixture obtained under point d); [0038] g) keep stirring for a time sufficient to homogenise the mixture; [0039] h) optionally, cooling the composition below the melting temperature of the fatty matter; [0040] i) optionally, screening the obtained compound to ensure homogeneity of particle size.

[0041] The methods described above can be carried out in any order of succession.

[0042] Optionally, the processing is carried out at a temperature equal to or higher than +64° C., the melting point of cannabidiol.

[0043] Preferably, for a better drying of the granulate, step g) is carried out under vacuum, at a temperature equal to or higher than 20° C.

[0044] The following examples illustrate the invention in greater detail.

DEFINITIONS

[0045] A fatty matter is defined as a fat, wax or a mixture of fats approved for food or pharmaceutical use such as, for example: vegetable oil, animal or vegetable butter, margarines or other hydrogenated fats, purified triglycerides, mono- or di-glycerides of fatty acids, polyethers such as polyethylene or polypropylene glycols, polyalcohols and the esters thereof with fatty acids. Preferably, said fatty matter has a melting point ranging between +30° C. and +80° C., more preferably between +35° C. and +70° C.

[0046] A pharmaceutically acceptable excipient is defined as an excipient useful in the preparation of a pharmaceutical formulation and generally regarded as safe, non-toxic and administrable to humans and animals.

EXAMPLE 1

[0047] Preliminary tests to study the formulations: an ademetionine salt was mixed with various fatty matters and the stability of the active substance was evaluated.

[0048] For each experiment, 485 g of mixed sulphate/p-toluenesulphonate salt with 51.5% (w/w) of ademetionine-ion, corresponding to 250 grams of active substance, mixed with the components shown in Table 1, were used.

TABLE-US-00001 TABLE 1 Compositions of ademetionine and fatty matter Test Composition Amount A Stearin 20 g Phosphatidylcholine 10 g B Stearin 30 g C Stearin 20 g Soya lecithin 10 g D Stearic acid 30 g E Olive oil 20 g Soya lecithin 10 g F MCT 30 g Soya lecithin 10 g Sucrose esters 10 g G Phosphatidylcholine 40 g H Soya lecithin 50 g

[0049] Stearin is a mixture of purified oleic and stearic acids, MCT (medium chain triglycerides) is a mixture of purified medium chain triglycerides.

[0050] The general processing method comprises: [0051] a) dosing the fatty matter and heat it until it melts; [0052] b) dosing the excipients; [0053] c) dissolving the excipients in the melted fatty matter; [0054] d) dosing the ademetionine salt; [0055] e) mixing the solution obtained under point c) with ademetionine; [0056] f) keep stirring for about 30 minutes; [0057] g) cooling the composition below +30° C.

[0058] In the case of test F it was sufficient to heat to +45° C., in the other tests to +60/70° C.; in test E no heating was necessary. All compositions were then screened on a 500-micron steel mesh sieve.

[0059] All preparations have proved to be low hygroscopic, free flowing and easy to process; the stability of ademetionine, as reported below, is more than satisfactory.

EXAMPLE 2

[0060] The composition was prepared comprising:

TABLE-US-00002 ademetionine 250 g  CBD 20 g stearin 50 g soya lecithin 10 g

[0061] For ademetionine, the salt from Example 1 (480 g) was used, and for cannabidiol, a pure crystalline product with CBD 98% w/w (20.4 g) was used. The method of Example 1 was carried out, by dosing the CBD and the soya lecithin in the melted stearin.

[0062] A white powder was obtained containing ademetionine (as an ion) 44.1% by weight and CBD 3.6% by weight; THC was absent.

EXAMPLE 3

[0063] By operating as described in Example 2, the composition was prepared comprising:

TABLE-US-00003 ademetionine 250 g  CBD 40 g stearic acid 20 g phosphatidylserine 30 g soya lecithin 10 g

[0064] Ademetionine was added to the melted mixture of stearic acid, soya lecithin and phosphatidylserine.

[0065] A white powder was obtained with ademetionine (ion) 42.8% w/w, CBD 6.7% w/w, THC absent.

EXAMPLE 4

[0066] By operating as described in Example 2, the composition was prepared comprising:

TABLE-US-00004 ademetionine 250 g  CBD 10 g stearic acid 20 g phosphatidylserine 30 g sucrose esters 10 g

[0067] 13 g of hemp oil extract refined by distillation was used, with CBD 77% and THC less than 0.2%, by weight.

[0068] A white powder was obtained with ademetionine 44.7% w/w and CBD 1.8% w/w, THC<0.05% w/w.

EXAMPLE 5

[0069] By operating as described in Example 2, the composition was prepared comprising:

TABLE-US-00005 ademetionine 250 g CBD 25 g vegetable oil 49.5 g phosphatidylserine 30 g sucrose esters 10 g

[0070] A 46% (w/w) ademetionine preformulation stabilised with calcium oxide and calcium chloride (543 g) was used; the distillate described in Example 4 (32.5 g) was used for CBD. The vegetable oil used is a mixture of extra virgin olive oil-, rich in polyphenols, and of linseed oil, rich in polyunsaturated fatty acids (omega-3/6/9).

[0071] A whitish powder was obtained with ademetionine ion 37.5%, CBD 3.7%, alpha-linoleic acid 3.7%, traces of THC less than 0.1% (all percentages by weight).

EXAMPLE 6

[0072] By operating as described in Example 2, the composition was prepared comprising:

TABLE-US-00006 ademetionine 152 g CBD 150 g stearin 50 g medium chain triglycerides 134 g vegetable oil 30 g phosphatidylcholine 30 g

[0073] 330 g of stabilised ademetionine and 200 g of distilled CBD already described in Example 4 were used.

[0074] A whitish powder was obtained with ademetionine ion 20% and CBD 20%, THC about 0.05% (% by weight).

EXAMPLE 7

Stability of Ademetionine in the Compositions

[0075] The compositions prepared according to the previous examples were placed in dark glass jars in cabinets with temperature and relative humidity control (+40° C. and 75% RH), periodically checking the content of active substances. The stability of the raw material is used as a reference.

TABLE-US-00007 TABLE 2 stability of ademetionine in the compositions Time (months) % residual Sample 0 1 2 3 ion composition 1C 48.5 48.2 47.8 47.4 97.9% composition 2 44.1 43.8 43.5 43.1 97.7% composition 4 44.7 44.3 44.1 43.9 98.2% composition 5 20.6 20.5 20.3 20.1 97.6% Ademetionine 51.5 51.0 49.6 48.8 94.8% Stabilised adm 46.0 45.8 45.7 45.0 97.8% Stabilised adm: ademetionine stabilised with inorganic desiccants (see experiment 5). % residual ion: active substance content after three months as a percentage with respect to time zero.

[0076] The results show that the preparation of Example 1 letter C and the compositions of experiments 2, 4 and 5 are more stable than ademetionine sulphate/p-toluene sulphate. The stability of compositions 2 and 4 is similar to that of the ademetionine preformulation with inorganic desiccants used in experiment 5. Furthermore, all the granulates obtained are low hygroscopic and have good flowability.

[0077] Mixing with a fatty matter gave stable and easily usable compositions of ademetionine and fatty matter, with or without cannabidiol.

EXAMPLE 8

Stability of Cannabidiol in the Compositions

[0078] The compositions described in Example 7 were also analysed for CBD and THC content. A mixture of equal parts of ademetionine sulphate/p-toluene sulphate and pure cannabidiol, mixed in the absence of fatty matter, was used as a reference.

TABLE-US-00008 TABLE 3 CBD and THC content in the compositions Time (months) % residual 0 0 3 3 CBD Sample CBD THC CBD THC — composition 2 3.6 >0.05 3.4 0.06 94.4% composition 5 21.0 0.05 20.6 0.09 98.1% Reference 48.9 0.11 38.2 6.2 78.1% CBD and THC: content in mg/dose. residual CBD: active substance content after three months as a percentage with respect to time zero.

[0079] The results show how the cannabidiol in the compositions described above is stable, while it degrades in the reference mixture. Furthermore, the THC content in the compositions is always less than 0.5% by weight, whereas it increases significantly in the reference mix.

EXAMPLE 9

Preparation of the Capsules

[0080] The composition of Example 2 was used (with the appropriate excipients) for the preparation of capsules, dosing about 567 mg per capsule to obtain an average dosage of:

TABLE-US-00009 ademetionine 250 mg  CBD 20 mg colloidal anhydrous silica  3 mg magnesium stearate 10 mg

[0081] The capsules (double-zero measurement) were filled with a filling machine in a dehumidified environment at relative humidity of 40-45%, without encountering any difficulties or inconveniences.

EXAMPLE 10

Preparation of the Tablets

[0082] The compositions of Examples 2, 4 and 5 were used for the preparation of tablets with a punch machine, working in an environment at 40-45% RH.

[0083] Per single tablet, the following were dosed:

TABLE-US-00010 ademetionine 250 mg CBD 10-40 mg microcrystalline cellulose 70 mg colloidal anhydrous silica 3 mg magnesium stearate 10 mg

[0084] Plain tablets of suitable hardness were obtained according to the European Pharmacopoeia standards.

[0085] The tablets prepared as above were subjected to filming in the drum mixer using a methacrylic acid copolymer equal to about 45 mg per tablet. Film-coated tablets were obtained with a release profile corresponding to the gastro-resistance indications of the European Pharmacopoeia.

[0086] The tablets of composition 5 have swollen and deformed, while all the others are stable.

EXAMPLE 11

Drying of the Compositions with CBD

[0087] It was operated as described in Example 3, but the step of mixing the active substances was carried out under vacuum, as described in Example 11. Samples taken during processing gave the analysis reported in the table.

TABLE-US-00011 TABLE 4 residual humidity in ademetionine and CBD compositions Sample Phase KF Ademetionine powder dosage 2.7% Composition of ademetionine + mixing 4.3% CBD + fatty matter Composition of ademetionine + screening 1.3% CBD + fatty matter KF: residual humidity in % w/w according to Karl-Fisher.

[0088] The data show that, by carrying out the process under vacuum, a drying of the composition of ademetionine, cannabidiol and fatty matter can be obtained.

EXAMPLE 12

Further Compositions

[0089] Further compositions of ademetionine and CBD were prepared, by operating as described above but using the materials reported in the following table.

TABLE-US-00012 TABLE 5 Further compositions of ademetionine and CBD Test Composition Amount I Ryoto sugar ester P-1670 ® (E473) 20 g Sunflower lecithin 10 g CBD L Ryoto sugar ester P-1570 ® (E473) 20 g Sunflower lecithin 10 g CBD M Geleol NMB ® (E471) 20 g Sunflower lecithin 10 g CBD N Ligamed SA-1-V ® 20 g Sunflower lecithin 10 g CBD O Admul MG ® (E471) 20 g Sunflower lecithin 10 g CBD

[0090] Where: Ryoto sugar ester P-1670® and P-1570 are mixtures of mono- and tri-glycerides of fatty acids, Geleol NMB® is a glyceryl palmite stearate, Ligamed SA-1-V® is a mixture of stearic and palmitic acid. All excipients at room temperature are presented as waxes or solids with a low melting point (<70° C.). For the preparation it is operated as described in Example 1, by heating until the fatty matter melts before adding ademetionine.

[0091] All the preparations obtained (granulates) have proved to be low hygroscopic, flowable and easy to process.

[0092] The stability of ademetionine was verified in a similar way to that reported in experiment 2: in all preparations the residual ademetionine titre after 3 months is greater than 97% of the initial titre.

EXAMPLE 13

Compositions of Ademetionine and CBD with Polyethylene Glycols

[0093] Compositions of ademetionine, cannabidiol and fatty matter are prepared, by operating as described in Example 2 using the salt of ademetionine 51.5% (480 g) and pure CBD 98% (20.4 g). The ingredients reported in the following table were used as the fatty matter.

TABLE-US-00013 TABLE 6 Compositions of ademetionine, CBD and polyethylene glycols Test Composition Amount P Polyethylene glycol 4000 20 g Sunflower lecithin 10 g CBD Q Polyethylene glycol 6000 20 g Sunflower lecithin 10 g CBD R Stearin 10 g Polyethylene glycol 4000 10 g Sunflower lecithin 10 g CBD

[0094] All the preparations obtained were granulated and have proved to be low hygroscopic, flowable and easy to process.

[0095] The stability of ademetionine was verified in a similar way to that reported in experiment 2: in all preparations the residual ademetionine titre after 3 months is greater than 97% of the initial titre.