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    • 专利摘要:
    Characteristic active ingredients for the prevention and / or treatment of various changes and pathological conditions caused by free radicals include acetyl L-carnitine and α-lipoic acid, and are dietary supplements, dietary supplements or practical Disclosed are compositions that can take the form of a medicament.
    公开号:KR20010079699A
    申请号:KR1020017002527
    申请日:1999-08-19
    公开日:2001-08-22
    发明作者:카바쟈클라우디오
    申请人:피에트로 폴라；시그마-타우 헬스사이언스 에스.피.에이；
    IPC主号:
    专利说明:

    Antioxidant composition comprising acetyl L-carnitine and α-lipoic acid
    [7] Systemic deficiency of alkanoyl L-carnitine (a natural compound present everywhere, and most importantly found in skeletal and myocardium at the highest concentrations) causes muscle and functional deficits, which are restored to normal by outpatient administration of the compound Can be.
    [8] Acetyl L-carnitine has been identified at both cerebral levels and peripheral neural tissues that require this for normal neurotransmission.
    [9] Energy production by carnitine occurs not only through β-oxidation of the fatty acids in the mitochondria, but also through the oxidation of branched chain amino acids and the regulation of insulin activity.
    [10] For the characterization of the biological activity of carnitine, studies pointing to the stabilizing effect of the carnitine on the integrity and deformability of the phospholipid membranes of cells and erythrocytes are important.
    [11] Acetyl L-carnitine protects cerebral tissues, especially against peroxidation. Although carnitine has been shown to be necessary for normal growth, it is also true that carnitine levels have been detected during aging compared to normal levels.
    [12] During the course of metabolism associated with aging, an increase in the oxidation process is steadily detected with an increase in the associated free radicals (which promote the onset of diabetic disorders).
    [13] Reduced mitochondrial activity increases the oxidant, which cell defenses can no longer effectively counter.
    [14] Increases in peroxides, hydroxides and free radicals produced by aerobic metabolism can damage macromolecules (DNA, proteins and lipids), which contributes to the initiation of degenerative diseases, including diabetes, which usually occurs during aging. Reduction of mitochondrial activity that occurs with aging also reduces cardiolipin, a diphosphatyl-glycerol derivative that forms part of the mitochondrial membrane structure and plays an important role in maintaining mitochondrial activity, particularly at the level of fatty acid β-oxidation processes. Entails. Mitochondrial activity including the fatty acid β-oxidation process can be reactivated by administration of acetyl L-carnitine, which can also restore cardiolipin concentration of mitochondria to normal.
    [15] The positive effect of acetyl L-carnitine on mitochondrial activity is also evidenced by its ability to promote the use of this pathway for ATP production. This effect is especially detected at the nerve level where acetyl L-carnitine has been shown to be able to prevent neurological disorders or chronic neurodegeneration.
    [16] During aging, in addition to the reduction of carnitine present in the body, a decrease in growth factor (GF-I) and in particular a decrease in IGF-I (insulin-like growth factor) is also detected.
    [17] IGF-I, IGF-II and relaxin are peptides belonging to the proinsulin group, also called somatomedin.
    [18] IGF exerts homeostasis and nutritional action, particularly at both central and peripheral nervous system levels, and clinical use of these peptides has produced favorable results for many degenerative neurological diseases, including diabetic neuropathy.
    [19] The correlation present between aging and the reduction of carnitine and growth factors (including IGF-I), and the recovery of these factor levels by outpatient administration of acetyl L-carnitine may be useful in the prevention and treatment of neurodegenerative diseases including diabetic neuropathy. Justify interest in carnitine for use.
    [20] α-lipoic acid has also been shown to perform important regulatory functions on carbohydrate metabolism and insulin activity. α-lipoic acid is actually widely distributed in both the plant and animal kingdoms and can be consumed as food. Initially recognized as a growth factor for many microorganisms, it was isolated from the bull's liver as bound to many animal proteins. It serves as an important scavenger of free radicals, in particular free radicals derived from environmental pollution. In recent years, the compounds have been shown to be quite useful for the regulation of glucose utilization and insulin activity to constitute an important factor in the prevention of diabetic neuropathy.
    [21] It has been demonstrated that increasing lipid peroxidation in diabetic neuropathy can be controlled and reduced at both cerebral levels and sciatic nerve or eye lens levels by administration of α-lipoic acid or one of its enantiomers. Moreover, α-lipoic acid inhibits aldose reductase activated by hyperglycemia, and thus α-lipoic acid may also play an important therapeutic role in diabetic complications.
    [22] α-lipoic acid improves insulin-induced muscle utilization of glucose and reduces the resistance of the insulin effect to glucose in diabetic patients. The antioxidant effect of α-lipoic acid is also associated with its neuro-protective ability against brain damage caused by ischemia and its putative therapeutic effect in Parkinson's disease and AIDS.
    [23] The antioxidant effect of α-lipoic acid may be direct or indirect through the recovery of glutathione and ascorbic acid concentrations.
    [24] The action of α-lipoic acid on carbohydrate metabolism is essential for its ability to act as a coenzyme in the oxidative decarbohydroxylation of pyruvate and other α-keto acids and to activate the tricarboxylic acid cycle to form ATP through acetate. However, it should also be borne in mind that there are other pathways in which α-lipoic acid exerts protective effects in order to account for the many beneficial biological effects of the compound on the prevention of diabetic damage.
    [25] Among them, particularly after reduction to dihydrolipoic acid, it inhibits the activation of nuclear transcription factor (NF-kB) by reactive oxygen species (ROS) and thus achieves its ability to dependently inhibit the associated neurotoxic and cytotoxic factors. Keep in mind the mechanism.
    [26] Since a number of complications associated with diabetes, such as neuropathy and cataracts of the eye, are mediated by ROS, inhibiting the activation of the nuclear transcription factor may lead to the prevention of α-lipoic acid in diseases associated with diabetes. It can be established through mechanism. Moreover, it should also be borne in mind that in diabetic patients the concentration of α-lipoic acid is lower than normal and these levels can be restored by administration of α-lipoic acid. Thus it has an additional effect on the effect of insulin on the transport of glucose to the cell membrane.
    [27] Chronic exposure to high concentrations of glucose can lead to non-enzymatic reactions between glucose and protein and spontaneous formation of highly reactive proteins known as end products of glycosylation (advanced glycosylation end product = AGE). The most studied of these are the glycosylation products of glucose and albumin, glucose and collagen, and glucose and hemoglobin. The effects AGE produces in tissues and cells are all related factors in explaining that diabetes occurs at a high rate at the nerve, muscle and endothelial levels.
    [28] Indeed, AGE improves the synthesis of extracellular matrix components, increases endothelial permeability and the formation of immune complexes and cytokines, and causes neuronal and retinal ischemia, myelin accumulation and myelin degeneration. Many of these compounds are formed during both diabetes and the aging process.
    [29] The correlation between AGE and activation of NF-IKB has recently been demonstrated as α-lipoic acid has the ability to inhibit this response.
    [30] Thus, protein glycosylation and glucose oxidation by high concentrations of glucose together with free radicals may be another cause for tissue abnormalities, particularly neural tissue abnormalities, associated with diabetes. The presence of α-lipoic acid also inhibits or limits the progression of glycosylation or glucose oxidation reactions.
    [31] Another protective effect of α-lipoic acid was also observed in pancreatic cells in contact with inflammatory factors.
    [32] Regarding the action of α-lipoic acid in the prevention and treatment of cataracts, the α-lipoic acid not only contributes to the other mechanisms described above, but also reduces vitamin C concentration in the eye due to hyperglycemia due to competition with glucose for vitamin C transport. May contribute to recovery.
    [33] In addition to saving vitamin E and increasing glutathione concentrations, the protective action of α-lipoic acid on the onset of neuropathy has also been confirmed by clinical studies. It was also observed that the reduction in neurological disorders was also accompanied by a decrease in the peroxidation response as detected by the drop in malonaldehyde concentration. Studies of several other institutions have demonstrated their activity in the treatment of diabetic neuropathy.
    [1] The present invention relates to tissue-related diseases caused by the presence of free radicals due to environmental pollution; Brain or myocardial injury caused by free radicals following cerebral or myocardial ischemia and concomitant reperfusion; A composition for the prophylaxis and / or treatment of metabolic disorders for toxic or diabetic neuropathy and glucose use.
    [2] Thus, the composition may take the form and exert its action in the form of a dietary supplement or an actual medicinal product depending on the supportive or prophylactic action, or strictly the therapeutic action, wherein the composition has no effect on the particular individual used. It is supposed to be exercised.
    [3] More particularly, the present invention
    [4] (a) acetyl L-carnitine or a pharmacologically acceptable salt thereof, and optionally one or more other "carnitines", where "carnitine" is L-carnitine, or propionyl L-carnitine, valeryl L-carnitine and iso Alkanoyl L-carnitine selected from the group comprising valeryl L-carnitine, or a pharmacologically acceptable salt thereof); And
    [5] (b) α-lipoic acid
    [6] Oral, parenteral, rectal or transdermal administrable composition comprising together.
    [34] Surprisingly, a composition comprising (a) acetyl L-carnitine or a pharmacologically acceptable salt thereof as a feature component, and (b) α-lipoic acid, may comprise tissue damage caused by the presence of free radicals due to environmental pollution; Brain or myocardial disorders caused by free radicals following cerebral or myocardial ischemia and reperfusion; It has been found to be highly effective in the prevention and / or treatment of metabolic disorders for toxic or diabetic neuropathy and glucose use.
    [35] Also advantageously, component (a) comprises a “carnitine” selected from the group comprising L-carnitine, propionyl L-carnitine, valeryl L-carnitine and isovaleryl L-carnitine or a pharmacologically acceptable salt thereof. It has been found that it may be further included.
    [36] The weight to weight ratio of (a) :( b) is in the range of 100: 1 to 1:10.
    [37] Toxicity test
    [38] Carnitine and α-lipoic acid are well known for their very limited toxicity and good tolerance. These advantageous toxicological characteristics of carnitine and α-lipoic acid were confirmed by combining these ingredients and administering them at high doses to both rats and mice. Indeed in these animals it is not only possible to orally administer 250 mg / kg or more of acetyl L-carnitine or 100 mg / kg of α-lipoic acid without the death of animals treated as follows, but also a mixture of 250 mg / kg of carnitine (Acetyl L-carnitine, propionyl L-carnitine, isovaleryl L-carnitine combined in a weight ratio of 1: 1 with each other) and acetyl L-carnitine of 500 mg / kg or more, carnitine mixture of 500 mg / kg and 200 It has been found that oral administration of mg / kg of α-lipoic acid is possible.
    [39] In addition, prolonged administration of 200 mg / kg of acetyl L-carnitine or 200 mg / kg of carnitine mixture with 100 mg / kg of α-lipoic acid via food for 30 consecutive days in both rat and mouse groups is well tolerated. No signs of toxicity were detected. Weight gain and various blood-chemical tests performed on these animals all showed normal values as found in histopathological tests performed on major organs after killing the animals at the end of the treatment.
    [40] Neuroprotective activity test for experimental cerebral ischemia
    [41] In view of the fact that disorders due to cerebral ischemia are associated with the production of free radicals and nitric oxide, both carnitine and α-lipoic acid provide protection against the toxic effects of free radicals, in this study endothelin-1 (120 pmol in 3 nl) ) Is injected into the anesthetized rat within 3 minutes using a microcannula placed on the gourd cortex at the level of the middle cerebral artery, according to the method disclosed in Scharkey, Y., Nature 371-336, 1994. Cerebral ischemia was induced by occlusion of the artery (MCA). Ischemia resulting from the occlusion of the arteries can be examined 3 days after the procedure by mesial perfusion of paraformaldehyde (4% in PBS) solution.
    [42] After the brain was removed, it was placed in a fixed solution containing 10% sucrose and the cryostat portion (20 nm) fixed with cresyl violet was examined under an optical microscope. Acetyl L-carnitine (50 mg / kg), or a carnitine mixture (where acetyl L-carnitine, propionyl L-carnitine and isovaleryl L-carnitine are combined in a weight ratio of 1: 1 with each other), or α-lipoic acid ( 20 mg / kg) was administered intravenously 5 minutes after the endothelin injection.
    [43] The volume of infarcted areas is described by Park C.K., Anns. Neurol., 20-150, 1989]. The results of these tests show that acetyl L-carnitine, carnitine mixtures and α-lipoic acid can all reduce the ischemic region, but surprisingly the most significant result is the combination of these products, especially the combination of acetyl L-carnitine with α-lipoic acid. Prove that it can be obtained by.
    [44]
    [45] Experimental Diabetic Hyperglycemia Test
    [46] Hyperglycemia is one of the underlying factors responsible for diabetes and in particular diabetic neuropathy, whether through the formation of protein glycosylation products (AGEs) or through metabolic hypoxia.
    [47] Therefore, regulation of serum glucose is one of the most important means for the prevention of diseases associated with diabetes. In this test, experimental diabetes was induced in rats, and then a test was performed to determine if the induced hyperglycemia could be reduced by acetyl L-carnitine, or carnitine mixture, or α-lipoic acid, or a combination of these products. . The hyperglycemia was caused by subcutaneous infusion of alloxane (100 mg / kg) in rats and the rats were considered hyperglycemic rats given serum glucose levels above 450 mg / dL on day 7 after the alloxan injection. .
    [48] Treatment with the test materials was given orally for 3 weeks. At the end of this period, serum glucose was measured for both groups of hyperglycemia and treated rats.
    [49] The results obtained demonstrate that the two carnitines and α-lipoic acid alone can only slightly reduce high initial serum glucose values, but the most significant results appear after administration of carnitine in combination with α-lipoic acid. Especially when a combination of acetyl L-carnitine and α-lipoic acid is used, there is a marked synergistic effect of these two products which can lower serum glucose values to near normal levels.
    [50]
    [51] Test for Sorbitol Content in the Ocular Lens and Sciatic Nerve of Diabetic Rats
    [52] Disorders caused by diabetic hyperglycemia and one of the most common causes of eye or peripheral neuropathy associated with diabetic hyperglycemia are the intracellular accumulation of sorbitol, thereby reducing osmotic capacity and cell integrity.
    [53] This test was performed in a group of rats that caused diabetes by intravenous administration of streptozotocin 50 mg / kg. One week after infusion, serum glucose was tested and rats with serum glucose values of 450 mg / dl or higher were considered diabetic rats. These animals were then continuously mixed with acetyl L-carnitine (100 mg / kg) or carnitine mixture (acetyl L-carnitine + propionyl L-carnitine + isovaleryl L-carnitine in a weight ratio of 1: 1 with each other for 8 days in a row. (100 mg / kg) or α-lipoic acid (25 mg / kg) alone or in various combinations.
    [54] After 8 days of treatment, after appropriate isolation, the concentration of sorbitol present in both sciatic nerve and eye lens of the diabetic rats was measured before and after administration. Although sorbitol concentrations were shown to be reduced in all treated animals, the most significant decrease was detected in animals treated with α-lipoic acid and carnitine, with the lowest reported in the group treated with acetyl L-carnitine and α-lipoic acid. .
    [55] The results of these tests also show a surprising synergistic potency activity between α-lipoic acid and carnitine.
    [56]
    [57] Survival and Growth Testing of Neurons Treated with IGF-I, Carnitine and α-Lipoic Acid
    [58] In view of the fact that insulin-like growth factor (IGF-I) plays an important role in protecting neuronal function integrity, particularly against toxic disorders such as disorders that occur during the course of diabetes, the present inventors have found that the growth and survival of brain cells is beneficial. It was considered whether the activity of IGF-I was promoted by the presence of carnitine, or α-lipoic acid, or a combination of these products in the culture medium. To this end, the brain cells of Wistar rats are described in Thanguipon W., Dev. Brain Res., 11, 177. 1983, isolated and dispensed onto plates at a density of 3 × 10 5 / cm 2 . Cytosine arabino-furanoside (10 mM) was added to the culture medium to prevent replication of non-neuronal cells. After 8 days, the cells were washed and serum maintained in medium replaced with BME (basic Eagle's medium, Life Technologies, Gaithersburg, MD) containing 5 mM concentration of KCl. Serum prepared as above alone or with test products, i.e., IGF-I, acetyl L-carnitine (100 ng / ml) or carnitine mixture (100 ng / ml) or α-lipoic acid, corresponding to 25 ng / ml or It was added directly together.
    [59] Cell survival and growth in culture are described by Jones K. H., J. Histochem. Cytochem., 33, 77, 1985 was observed 24 hours after addition of the materials to the medium on a 35 mm disc in contact with 10 ng / ml of fluorescein acetate. Cell counts were counted using a fluorescence microscope. The results of this test show that the growth-promoting effect of IGF-I on isolated brain cells is markedly enhanced by the presence of carnitine and α-lipoic acid (they alone do not produce significant changes) and maximizes growth. The potentiating effect indicates that carnitine, and especially acetyl L-carnitine, is used when used with α-lipoic acid.
    [60]
    [61] Sciatic Nerve Regeneration Testing in Diabetic Rats
    [62] Diabetic induced rats with sciatic nerve removed have inferior regenerative activity than normal rats.
    [63] This test was performed to investigate whether regeneration of the sciatic nerve in diabetic rats can be promoted by treatment with acetyl L-carnitine, carnitine mixture, or α-lipoic acid, or a combination of these products. The techniques used in these tests are described by Fernandez E., Int. J. Clin. Pharmacol. Res., 10, 85, 1990.
    [64] Subcutaneous injection of 100 mg / kg of alloxanes induced diabetes (serum glucose of 450 mg / dl or more) in the rat group. Acetyl L-carnitine, carnitine mixture and α-lipoic acid, 1: 1 acetyl L-carnitine (200 mg / kg), carnitine mixture (acetyl L-carnitine + propionyl L- carnitine + isovaleryl L-carnitine (200 mg / kg) and α-lipoic acid (50 mg / kg) were administered together with the food. The compounds were administered one week before sciatic nerve removal and 30 days after removal.
    [65] The sciatic nerve was removed after anesthesia with 1 cm of nerve exposed at the level of the sciatic cavity. The boundaries of the injury are indicated by extraneural sutures. Thirty days after the nerve cutting, the animals were killed and the shin nerve tissue, one of the major compartments of the sciatic nerve, examined. Four cross-sections of the shin nerve, approximately 4 mm long, were performed morphologically and morphometrically by a Zeiss Videoplan Image Analyser.
    [66] The number of regenerated sides and its density, and regenerated elements per 100 nm 2 were measured. It has thus been demonstrated that it is possible to measure the diabetic-induced degeneration of the shin nerve elements, and the degeneration was corrected to almost normal levels by treatment with acetyl L-carnitine, carnitine mixture and α-lipoic acid.
    [67] The most obvious results with regard to the prevention of diabetic damage to nerve regeneration are those obtained by administering an acetyl L-carnitine or carnitine mixture in combination with α-lipoic acid, which is therefore a significant and unexpected for the combination part according to the invention. To demonstrate synergy.
    [68]
    [69] Neuromuscular conduction test
    [70] One of the most obvious abnormalities in peripheral neuropathy, and particularly diabetic neuropathy, is the slowing of neuromuscular conduction reflected in changes in motor activity.
    [71] In this test, we induced experimental diabetes in rats by intravenously injecting 50 mg / kg of streptozotocin into experimental animals (rats of average body weight 300 g). In animals induced with diabetes (serum glucose 450 mg / dl or more), neuromuscular conduction rate (NMCV) was measured. To this end, the sciatic nerve (2 cm long) was isolated and the soleus muscle separated from the long and short muscles and their distal tendon cuts and connected to an isometric transducer that recorded muscle contractile force (MCF). The muscle was stimulated through the nerve using two electrodes inserted 10 mm from the sciatic nerve and connected to the stimulator.
    [72] A bipolar electrode was placed at the distal end of the muscle to show EMG through an oscilloscope.
    [73] NMCV was measured in m / sec by dividing the distance between the stimulation electrodes by the mean potential difference between the onset of ECG potential difference development at two sites. MCF is expressed in mm.
    [74]
    [75] Motor Synergy Abnormal Test
    [76] This test was tested in “stumble mice”, ie animals exhibiting wobbly gait, abnormal foot position and slow movement speed. This abnormality is particularly associated with the progressive degeneration of motor neurons and myofascial nerve fibers that affect the forelimbs. Tests are described in Mitsumoto H., Annal. Neurol., 36, 14. 1994]. After diagnosis, the staggered mice were subjected to acetyl L-carnitine (200 mg / kg), or carnitine mixture (200 mg / kg), or α-lipoic acid (50 mg / kg), or various combinations of these products for 20 consecutive days. Oral treatment with. In treated animals versus control, the test was performed by evaluating the time each animal was holding on the edge of the inclined platform (holding time) and the time it took to run a distance of 10 cm (running time).
    [77] The results of these tests show that treatment of these animals with acetyl L-carnitine, carnitine mixture and α-lipoic acid improves both the sustaining and running times as compared to the control, and together these products, in particular acetyl L-carnitine and α- It is indicated that the maximum effect is obtained by administering lipoic acid together. These tests also have significant and unexpected synergistic effects of carnitine and α-lipoic acid.
    [78]
    [79]
    [80] Cisplatin-induced sensory neuropathy test
    [81] Prolonged administration of cisplatin to experimental animals can cause disturbances at the sensory nerve level and cause significant abnormalities in hypersoluble perception.
    [82] In this test, the inventors used acetyl L-carnitine (300 mg / kg), or a carnitine mixture (acetyl L-carnitine + propionyl L-carnitine, for toxicity caused by subcutaneous injection of cisplatin 10 mg / kg for 7 consecutive days. + Isovaleryl L-carnitine formulated at a weight ratio of 1: 1) (300 mg / kg), or α-lipoic acid (50 mg / kg), or various combinations of these products for 7 days orally The protective effect exerted was evaluated.
    [83] The hypersoluble sensory perception induced by cisplatin in mice was assessed by the Rotarod test (Apfel, S.C., Ann. Neurol., 29, 89, 1991).
    [84] The results obtained in these tests showed that cisplatin significantly reduced equilibrium time in cisplatin-treated animals compared to control animals and to the same extent in animals treated with acetyl L-carnitine or α-lipoic acid alone, whereas Animal groups treated with α-lipoic acid demonstrate that they exhibit substantially the same equilibrium capacity as those without cisplatin poisoning. These tests also have a marked synergistic effect of carnitine and α-lipoic acid.
    [85]
    [86] Tests were conducted to evaluate the ability of the novel compositions to fully justify the innovative properties of the present invention and to demonstrate all of the above surprising surprising synergistic effects that can be caused when the components are used together.
    [87] Based on the synergistic action of the components of the compositions according to the invention disclosed herein, the compositions are suitable for the prevention of toxic and metabolic damage causing acute or chronic neurological disorders. In particular, the composition can be used for the treatment of toxic neuropathy, in particular diabetic peripheral neuropathy.
    [88] The composition is also indicated in view of its antioxidant capacity to be used for the prevention or treatment of toxic or oxygen deficiency abnormalities associated with the release of free radicals of the brain, liver, heart or other organs and tissues.
    [89] Moreover, in view of the ability of the composition to promote the action of IFG-I, satisfactory benefits can also be obtained from the use of the composition for pathological abnormalities associated with aging, such as neurodegenerative diseases.
    [90] Illustrative, non-limiting examples of formulations according to the invention are shown below:
    [91] 1) Acetyl L-Carnitine 500 mg
    [92] α-lipoic acid 50 mg
    [93] 2) 500 mg of carnitine mixture
    [94] (Equivalent weights of acetyl L-carnitine, propionyl L-carnitine,
    [95] Isovaleryl L-carnitine)
    [96] α-lipoic acid 50 mg
    [97] 3) Acetyl L-Carnitine 250 mg
    [98] α-lipoic acid 25 mg
    [99] 4) 250 mg of carnitine mixture
    [100] (Equivalent weights of acetyl L-carnitine, propionyl L-carnitine,
    [101] Isovaleryl L-carnitine)
    [102] α-lipoic acid 25 mg
    [103] 5) Acetyl L-Carnitine 1 mg
    [104] α-lipoic acid 100 mg
    [105] 6) Acetyl L-Carnitine 250 mg
    [106] α-lipoic acid 25 mg
    [107] Selenium Methionine 50mg
    [108] Zinc Glycinate 10 mg
    [109] Magnesium Stearate 20 mg
    [110] Taurine 50 mg
    [111] Vitamin E 10 mg
    [112] CoQ10 10 mg
    [113] β-carotene 10 mg
    [114] Vitamin C 30 mg
    [115] What is meant by pharmacologically acceptable salts of L-carnitine or alkanoyl L-carnitine are any salts with these active ingredients and acids that do not produce unnecessary toxicity or side effects. These acids are well known to experts in the field of pharmacy.
    [116] Non-limiting examples of suitable salts include the following: chloride; Bromide; Iodide; Aspartate, acid aspartate; Citrate, acid citrate; Tartrate; Phosphates, acid phosphates; Fumarate, acid fumarate; Glycerophosphate; Glucose phosphate; Lactates; Maleate, acid maleate; Orotate; Oxalate, acid oxalate; Sulfates, acid sulfates; Trichloroacetate; Trifluoroacetate and methanesulfonate.
    [117] A list of FDA-approved pharmacologically acceptable salts is described in Int. J. of Pharm. 33 (1986), 201-217, which is incorporated herein by reference.
    [118] The composition according to the invention may also comprise vitamins, coenzymes, mineral substances and antioxidants.
    [119] Suitable excipients for use in the preparation of the compositions given the particular route of administration will be apparent to those skilled in the pharmaceutical and food industry.
    [120] As mentioned above, the composition according to the present invention comprises a tissue-related disease caused by the presence of free radicals due to environmental pollution; Brain or myocardial injury caused by free radicals following cerebral or myocardial ischemia and concomitant reperfusion; It can be usefully used for the prevention and / or treatment of metabolic disorders for toxic or diabetic neuropathy and glucose use.
    权利要求:
    Claims (13)
    [1" claim-type="Currently amended] (a) acetyl L-carnitine or a pharmacologically acceptable salt thereof; And
    (b) α-lipoic acid
    Composition comprising together.
    [2" claim-type="Currently amended] A compound according to claim 1, wherein component (a) is selected from the group comprising L-carnitine, propionyl L-carnitine, valeryl L-carnitine, isovaleryl L-carnitine and pharmacologically acceptable salts and mixtures thereof. A composition further comprising “carnitine”.
    [3" claim-type="Currently amended] The composition according to claim 1 or 2, wherein the weight ratio of (a) :( b) is 100: 1 to 1:10.
    [4" claim-type="Currently amended] The method according to claim 1, wherein the pharmacologically acceptable salt of L-carnitine or alkanoyl L-carnitine is selected from the group consisting of chloride; Bromide; Iodide; Aspartate, acid aspartate; Citrate, acid citrate; Tartrate; Phosphates, acid phosphates; Fumarate, acid fumarate; Glycerophosphate; Glucose phosphate; Lactates; Maleate, acid maleate; Orotate; Acid oxalate; Sulfates, acid sulfates; Trichloroacetate; A composition selected from the group comprising trifluoroacetate and methanesulfonate.
    [5" claim-type="Currently amended] The composition of claim 1, further comprising vitamins, coenzymes, mineral substances and antioxidants.
    [6" claim-type="Currently amended] 6. The composition of claim 1 in the form of an orally administrable dietary supplement. 7.
    [7" claim-type="Currently amended] 7. A composition according to any one of claims 1 to 6 in the form of a pharmaceutical which is oral, parenteral, rectal or transdermal.
    [8" claim-type="Currently amended] Prevention of tissue damage caused by the presence of free radicals due to environmental pollution; Prevention of brain or myocardial damage caused by free radicals following cerebral or myocardial ischemia and concomitant reperfusion; The dietary supplement of claim 6 for the prevention of metabolic disorders for diabetic or toxic neuropathy and glucose use.
    [9" claim-type="Currently amended] Diseases caused by the presence of free radicals due to environmental pollution; Brain or myocardial injury caused by free radicals following cerebral or myocardial ischemia and concomitant reperfusion; Atherosclerotic damage and tissue proliferative processes; The agent of claim 7 for the treatment of metabolic disorders for diabetic or toxic neuropathy and glucose use.
    [10" claim-type="Currently amended] 9. A dietary supplement according to claim 6 or 8 in the form of a solid, semi-solid or liquid.
    [11" claim-type="Currently amended] 12. A medicament according to claim 9 or 11 in the form of a solid, semi-solid or liquid.
    [12" claim-type="Currently amended] The dietary supplement of claim 10 in the form of a tablet, lozenge, pill, capsule, granule or syrup.
    [13" claim-type="Currently amended] 12. A pharmaceutical according to claim 11 in the form of tablets, lozenges, pills, capsules, granules, syrups, vials or drops.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1998-09-01|Priority to ITRM98A000566
    1998-09-01|Priority to IT1998RM000566A
    1999-08-19|Application filed by 피에트로 폴라, 시그마-타우 헬스사이언스 에스.피.에이
    1999-08-19|Priority to PCT/IT1999/000268
    2001-08-22|Publication of KR20010079699A
    2003-08-27|First worldwide family litigation filed
    优先权:
    申请号 | 申请日 | 专利标题
    ITRM98A000566|1998-09-01|
    IT1998RM000566A|IT1302307B1|1998-09-01|1998-09-01|Composition to attivita 'antioxidant and adapted to metabolic glucose migliorarel'utilizzazione, comprising acetyl|
    PCT/IT1999/000268|WO2000011968A1|1998-09-01|1999-08-19|ANTIOXIDANT COMPOSITION COMPRISING ACETYL L-CARNITINE AND α-LIPOIC ACID|
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