Hydrosoluble organic salts of creatine

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof

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C07C24100

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active

059731990

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BRIEF SUMMARY
The present invention refers to hydrosoluble organic salts of creatine of general formula I: ##STR1## wherein A.sup..crclbar. represents the anion of a mono, bi- or tricarboxylic acid. Preferred anions are the citrate, maleate, fumarate, tartrate or malate.
Creatine or N-(aminoiminomethyl)-N-methylglycine is a sarcosine derivative present in the muscle tissue of many vertebrates, man included, mainly combined with phosphoric acid in form of phosphorylcreatine and it is involved in the energy transfer from mitochondria to the ATP utilization sites.
Several studies indicate that there is a relationship between the creatine (phosphoryl creatine) concentration in the muscles having the function of keeping an high intracellular ATP/ADP ratio and maximum sustainable physical effort (Annu. Rev. Biochem. 54: 831-862, 1985; Science 24: 448-452, 1981; BESSMAN S. P., and F. SAVABI. The role of the phosphocreatine energy shuttle in exercise and muscle hypertrophy. In: Biochemistry of Exercise VII. A. W. Taylow, P. D. Gollnick, H. J. Green, C. D. Ianuzzo, E. G. Noble, G. Metivier, and J. R. Sutton., Intl. Series Sports Sciences 21: 167-178, 1990).
The creatine increase in diets may therefore be useful to bring the plasma creatine concentrations at levels providing significant values of creative itself in the muscle. The short creatine half-life in plasma (1-1.5 hours) makes however necessary to reach rapidly said levels and this, in view of the bioavailability degree of creatine, is obtainable only by the administration of high doses of 5-10 g (for mean body weights of 70 kg), amounts well tolerated because of the lack of toxicity of the compound.
The low solubility of creatine in water (1 g in 75 ml) is therefore a practical limitation to the possibility of marking immediately available in the specific diet the necessary amounts of creatine.
WO 94/02127, published on Feb. 3, 1994, discloses the use of creatine, optional combined with aminoacids or other components, in order to increase the muscle performance in mammals.
The present invention provides hydrosoluble stable organic salts of creatine of formula I characterized by high water solubility (from 3 to 15 times higher them that of creatine itself) and a process for their preparation. The salts of formula I are prepared by salifying creatine with the corresponding acids in aqueous or hydroalcoholic concentrated solution or in a water-immiscible solvent, at temperatures ranging from the room temperature to 50.degree. C., optionally concentrating the solutions and filtering the crystallized salts. According to a preferred embodiment the salts of formula I are prepared by reacting creatine with an excess organic acid in ethyl acetate until the salt is completely formed, detectable with the IR analysis, cooling and filtering. The filtrated solvent, containing the excess acid is recycled and, after filling up of the components, is used for a further reaction.
The salts are characterized by IR, melting point, potentiometric and HPLC assay.
Table 1 reports the solubility of the salts I of the invention.


TABLE 1 ______________________________________ Creatine salt Water solubility % (g/100 ml) ______________________________________ Citrate 10 Maleate 19 Fumarate 3 Tartarate 8,5 Malate 4,5 ______________________________________


EXAMPLE 1

39.45 g (0.18 mol) of monohydrate citric acid are suspended in 100 ml of ethyl acetate. 20 g (0.134 mol) of monohydrate creatine are added to the stirred suspension at 20-25.degree. C. and the mixture is stirred 4 hours at 25.degree. C. After IR control, the product is filtered and washed with ethyl acetate, then dried in oven at 50-55.degree. C., obtaining 90% of salts, m.p. 112-114.degree. C., 99.2% titer.


EXAMPLE 2

14.9 g (0.1 mol) of monohydrate creatine are added to a solution of 11.6 g (0,1 mol) of maleic acid in 20 ml of water. The so obtained solution is concentrated, cooled to 5.degree. C. and the product filtered and dried under vacuum at 50.degree. C., obtaining 87% of salt, m.p. 128-129.degree. C., 9

REFERENCES:
patent: 1967400 (1934-07-01), Fischl
patent: 4420432 (1983-12-01), Chibata
patent: 5091171 (1992-02-01), Yu
patent: 5387696 (1995-02-01), Kottenhahn
patent: 5489589 (1996-02-01), Wittman
patent: 5627172 (1997-05-01), Almada
Chemical Abstracts, vol. 84, No. 1, 1976 Columbus, Ohio, US; p. 13433.
ACTA Physiol. Scand. (1995) , 153 (2), 207-9 Coden: APSCAX: ISSN: 0001-6772, 1995 Earnest, C.P. et al.

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