WO2006061925A1 - フリーラジカル疾患予防治療用組成物 - Google Patents
フリーラジカル疾患予防治療用組成物 Download PDFInfo
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- WO2006061925A1 WO2006061925A1 PCT/JP2005/014798 JP2005014798W WO2006061925A1 WO 2006061925 A1 WO2006061925 A1 WO 2006061925A1 JP 2005014798 W JP2005014798 W JP 2005014798W WO 2006061925 A1 WO2006061925 A1 WO 2006061925A1
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- cancer
- fullerene
- free radical
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Definitions
- the present invention relates to a composition for the prevention and treatment of free radical diseases, which exhibits high preventive and therapeutic efficacy against various free radical-related diseases, and has high drug stability and low side effects in vivo. It is. Background art
- Fullerene molecules are composed of carbon atoms, and each sphere contains 32 to 100 or more carbon atoms.
- fullerenes see: (i) RE Sialley, “One Beam of Ultrasonic Carbon Cluster in Atomic and Molecular Classes”, E. LBerstein Ed., Physical theory chemistry, Vol. 68, Else Beer'Science (New York), pp. 1-68 (1990), (ii) F. Curl et al., “Fullerenes”, Scienti Fick American, pages 32 to 41 (October 1991), (iii) F.
- fullerenes The most typical of these fullerenes is C 60 fullerene. And its structure is reminiscent of football. There are other fullerenes, especially C70 and C84 as higher fullerenes. And fullerenes are now commonly known as “buckyballs”. C60 fullerene molecules generally contain small amounts of C70 fullerene and C84 fullerene as impurities. The preparation of fullerenes and their solubility, crystallinity and color properties are described in many literatures, especially in the paper by W. Kraetschmer et al. [Nature, 347, 354-358 (1990) ), And Chemical 'and' Engineering 'News, pages 22-25 (October 1990)].
- fullerenes With increasing interest in fullerenes, the application of fullerenes to pharmaceuticals and cosmetics has been studied and specific proposals have been made. For example, blending fullerenes or fullerene mixtures into cosmetics (Patent Document 1), making a cosmetic composition for suncare using the ultraviolet absorption effect of fullerenes (Patent Document 2), and using fullerene as a photosensitizer.
- the present inventors have proposed a method of optically inactivating viruses (Patent Document 3) and applying fullerene as an antioxidant to external preparations for skin (Patent Document 4).
- Non-patent Documents 1 and 2 diseases caused by in vivo free radicals (in the present invention, It has been pointed out that this is called free radical disease (Non-patent Documents 1 and 2). In fact, for the purpose of treating or preventing these free radical diseases, the development of drugs for the prevention and treatment of free radical diseases has been promoted for a long time, and many pharmaceutical ingredients such as the following have already been proposed. Yes.
- Non-patent Document 3 SOD-related substances (Non-patent Document 3), ubiquinone preparations (Patent Document 5), benzozevin derivatives (Patent Document 6), pyrrolidinone derivatives (Patent Document 7), substituted vinyl derivatives (Patent Document 8), oxamide derivatives (Patent Document 9), Furan Carpoxamide Derivative (Patent Document 10), Phthalimide Derivative (Patent Document 11), Docosahexaenoic Acid (Patent Document 12), Linolenic Acid Derivative (Patent Document 13) , Quinolinoxide derivatives (patent document 14), heteroaromatic amine derivatives (patent document 15), carbostyryl derivatives (patent document 16), isoindole derivatives (patent document 17), cell product (patent document) 1 8), imidazol thione carboxamide derivative (Patent Document 19), dipenzoxepin derivative (Patent Document 20), propylamine derivative (P
- the present invention is based on the present inventors' previous knowledge that fullerene is applied to a topical skin preparation as an antioxidant, and the above-mentioned conventional drugs for prevention and treatment of free radical diseases as described above.
- the problem is to provide a new composition for the prevention and treatment of free radical diseases that eliminates the problems associated with drugs, has few side effects, has high free radical scavenging activity in the body, and has excellent pharmaceutical stability. Yes.
- Patent Document 1 Japanese Patent Laid-Open No. 6-1 9 2 0 39
- Patent Document 2 Japanese Patent Laid-Open No. 9-2 7 8 6 2 5
- Patent Document 3 JP-A-9-3 2 2 7 6 7
- Patent Document 4 Japanese Patent Application Laid-Open No. 2004-2 5 0 6 90
- Patent Document 5 Japanese Patent Application Laid-Open No. Sho 5 71 4 2 6 1 6
- Patent Document 6 Japanese Patent Laid-Open No. Sho 5 7-1 9 3 4 6 2
- Patent Document 7 Japanese Patent Laid-Open No. 5-9-2 7 8 2 3
- Patent Document 8 Japanese Patent Application Laid-Open No. 60-0 2 8 96 3
- Patent Document 9 Japanese Laid-Open Patent Publication No. 5-9 1 6 3 3 5 3
- Patent Document 10 Japanese Patent Application Laid-Open No. 5 9-1 9 09 9 1
- Patent Document 11 Japanese Patent Application Laid-Open No. 6 1-3 7 7 6 6
- Patent Document 1 2 Japanese Patent Laid-Open No. 4-2 7 3 8 1 7 Patent Document 13: Japanese Patent Laid-Open No. 61-44853
- Patent Document 14 Japanese Patent Laid-Open No. Sho 6 1-1 6 5869
- Patent Document 15 Japanese Patent Application Laid-Open No. Sho 6 1 1 2 82377
- Patent Document 16 Japanese Patent Application Laid-Open No. Sho 63 1 3 0182 1
- Patent Document 17 Japanese Patent Laid-Open No. Sho 631-150276
- Patent Document 18 Japanese Patent Laid-Open No. 1-14 3868
- Patent Document 19 Japanese Patent Laid-Open No. 11-6820
- Patent Document 20 Japanese Patent Laid-Open No. 3-176487
- Patent Document 21 Japanese Patent Laid-Open No. 3-23 6378
- Patent Document 22 Japanese Patent Laid-Open No. 4-2 1 1666
- Patent Document 23 Japanese Patent Laid-Open No. 11-25726
- Patent Document 24 Japanese Patent Laid-Open No. Hei 41-330088
- Patent Document 25 Japanese Patent Laid-Open No. 54-4401
- Patent Document 26 Japanese Patent Laid-Open No. 2-30 8799
- Patent Document 27 Japanese Patent Laid-Open No. 4 1 3 1 2531
- Patent Document ⁇ 28 Japanese Patent Laid-Open No. 6-72 871
- Patent Document 29 Japanese Patent Laid-Open No. 6-107693
- Patent Document 30 JP-A-8-29 1075
- Patent Document 31 Japanese Patent Application Laid-Open No. Hei 10 1 3 3026 1
- Non-Patent Document 1 “Reactive Oxygen and Pathology” edited by Inoue, JS
- Non-patent document 2 “Antioxidant”: Futaki et al.
- Non-Patent Document 3 Inoue, et al., Biochemistry, 28, 66
- the present inventor has used vascular endothelial cells in vitro as an adult disease model.
- free radicals were generated by culturing and temporarily hypoxic, and fullerenes were allowed to act on them, it was confirmed that free radicals generated in cells were suppressed more than conventional vitamin C.
- fullerenes have significantly better stability, are less toxic in vivo, and can fully exert their effects, thereby completing the present invention.
- composition for preventing and treating free radical disease of the present invention is characterized by the following as a solution to the above problems.
- a composition for the prevention and treatment of free radical diseases comprising as an active ingredient at least one of fullerene, a fullerene derivative, or a fullerene modified or clathrated with an organic compound or a complex of fullerene derivatives. .
- the fullerene derivative is a fullerene that combines one or more of an oxygen-containing group, a nitrogen-containing group, and an optionally substituted hydrocarbon group.
- the first composition for preventing and treating free radical diseases object is a fullerene that combines one or more of an oxygen-containing group, a nitrogen-containing group, and an optionally substituted hydrocarbon group.
- the first composition for preventing and treating free radical disease wherein the fullerene is at least one selected from fullerene multimers, carbon nanotubes, derivatives thereof, and salts thereof.
- the first composition for preventing and treating free radical disease wherein the fullerene is at least one selected from a fullerene cleavage product, a fullerene fragment, a derivative thereof, and a salt thereof.
- Fullerenes are complexes of one or more of fullerenes and fullerene derivatives with one or more of organic oligomers, organic polymers, cyclodextrins and crown ethers and one or more of the related compounds.
- the composition for the prevention and treatment of any free radical disease is a complex of at least one of fullerene and fullerene derivatives and polyvinylpyrrolidone (PVP).
- composition for preventing and treating free radical disease according to any one of the first to fifth, wherein the fullerene is represented by the following formula.
- F is a fullerene represented by C n (C is a carbon atom, n is an integer of 3 or more), carbon nanotubes, and their multimers, cleaved bodies, split bodies, or a mixture thereof.
- R im is m substituents bonded to C n, and each independently or independently represents a hydroxyl group, an ester group of the hydroxyl group and an inorganic acid or an organic acid, and a coordination of the hydroxyl group and a sugar.
- a saccharide group, a ketal group of its hydroxyl group and ketone, or an acetal group of its hydroxyl group and aldehyde R 2 m are m atoms bonded to C n, each independently being the same or Otherwise, or indicates that one atom is bonded to two or more different carbons, m represents 0 or an integer of 1 or more.
- C is a fullerene partial structure represented by a carbon atom, and it is sufficient that two or more carbon atoms are covalently bonded (if there is a carbon that is not covalently bonded, Even if there is no indication of R n, it will combine with R n Rn is n substituents bonded to C, and each independently or independently, a hydrogen atom, a carbon atom, an oxygen atom, a nitrogen atom, a phosphorus atom, a hydroxyl group, It represents an ester group of a hydroxyl group and an inorganic acid or an organic acid, a glycoside group of the hydroxyl group and a sugar, a ketyl group of the hydroxyl group and a ketone, or an acetal group of the hydroxyl group and an aldehyde.
- n represents an integer of 0 or 1 or more.
- composition for preventing or treating free radical diseases according to any one of the first to ninth, further comprising at least one antitumor agent.
- Anti-tumor agents include nitromine (R), cyclophosphamide, melphalan, thiotepa, force lupocon, Protecton (R), busulfan, dimustine hydrochloride, mitopurinitor, ifosfamide, mercaptopurin, thioinosine, Cytarabine, Dagarpazine, Fluorouracil, Tegafur, Anshiyubo hydrochloride, Methotrexate, Carmofur, UF T (R), Enoshibabin, Binplastin sulfate, Vincristine sulfate, Vindesine sulfate, Actinomycin (D), Mitomycin (:, Chromo Mycin A3, Bleomycin Hydrochloride, Bleomycin Sulfate, Daunorubicin Hydrochloride, Doxorubicin Hydrochloride, Neocarcinos Yuchin, Bepeptibromycin Sulfate, Acralubicin Hydro
- No. 12 Free radical disease, myocardial infarction, ischemic heart disease, heart failure, angina, arrhythmia, arteriosclerosis, liver lipid metabolism disorder, hyperlipidemia, essential hypertension Pressure, hypertension, arteriosclerosis, coronary arteriosclerosis, thrombosis, obstructive arteriosclerosis, vascular disorder, peripheral vascular disorder, cholestasis, hypercholesterolemia, knee disorder, organ failure, acute chronic hepatitis, Gastric ulcer, duodenal ulcer, ulcerative colitis, extinct organ disorder, cholecystosis, diabetes, arthritis treatment, rheumatism, liver failure, liver disorder, ischemic liver disorder, liver lipid metabolism disorder, gallbladder disorder, organ transplant disorder, sugar Urine disease, toxicosis, organ transplant disorder, cancer, ischemic reperfusion injury, tissue aging, skin tissue pigmentation, skin tissue fistula, alveolar pus leakage, skin tissue seborrhea, skin tissue sunburn, A composition for the prevention and
- Cancer is malignant melanoma, malignant lymphoma, digestive cancer, lung cancer, esophageal cancer, stomach cancer, colon cancer, rectal cancer, colon cancer, ureteral tumor, gallbladder cancer, bile duct cancer, biliary tract cancer, breast cancer, liver Cancer, knee cancer, testicular tumor, maxillary cancer, tongue cancer, lip cancer, oral cancer, pharyngeal cancer, laryngeal cancer, ovarian cancer, uterine cancer, prostate cancer, thyroid cancer, brain tumor, force positive sarcoma, hemangioma, leukemia
- the composition for preventing and treating free radical disease according to the above-mentioned 12, which is polycythemia vera, neuroblastoma, retinoblastoma, myeloma, cystoma, sarcoma, osteosarcoma, or myoma.
- Ischemic reperfusion injury ischemic heart disease, ischemic reperfusion myocardial injury, ischemic liver injury, ischemic reperfusion liver injury, ischemic reperfusion kidney injury, ischemic reperfusion knee injury, Ischemic reperfusion gallbladder disorder, ischemic reperfusion cardiovascular disorder, ischemic reperfusion gastrointestinal disorder, ischemic reperfusion myopathy, ischemic reperfusion vascular disorder, ischemic reperfusion ocular disorder, or ischemic reperfusion 12.
- the composition for preventing and treating free radical disease according to the above-mentioned first or second, which is a skin disorder.
- Item 17 The composition for preventing and treating free radical disease according to Item 12 above, wherein the infectious disease is a bacterial infection, a viral infection, a fungal infection, or a parasitic infection.
- No. 18 The composition for preventing and treating free radical disease according to No. 17 above, wherein the viral infection is hepatitis, acquired immune deficiency syndrome (AIDS), cold, or influenza. Brief Description of Drawings
- FIG. 1 is a diagram illustrating the effect of PVP / fullerene in suppressing metastasis of skin cancer in Test Example 5.
- FIG. 2 is a diagram exemplifying the effect of suppressing metastasis of cancer cells by PVP / fullerene in Test Example 6.
- the active ingredient or useful ingredient is the fullerene as described above, which is modified or clathrated with fullerene, a fullerene oxygen-containing derivative, and an organic compound. It consists of at least one of the above fullerenes or fullerene oxygen-containing derivatives and their salts.
- fullerenes are expressed as C n (n is an integer of 60 or more), including C 60, C 70, or a mixture thereof, and carbon tube fullerenes, etc.
- Various types including a conventionally known one having a carbon skeleton structure such as a spherical shape or a tube may be used.
- the fullerene of the invention of this application includes a combination of a plurality of fullerenes via an alkylene chain such as a methyle chain, or an alkylene chain bonded to carbon atoms at different positions of the fullerene skeleton. It may be a combination.
- 1 to 40 modifying groups may be bonded to one fullerene molecule.
- a modifying group is bonded to one fullerene molecule.
- 1 to 50 may be bonded to each other, and each of these modifying groups is independently a hydroxyl group, an ester group of the hydroxyl group with an inorganic or organic acid, or a glycoside group with a sugar, or a hydroxyl group. It may be a ketal group with a ketone or an acetal group with an aldehyde, and may be at least one selected from the fullerene-modified compound or a salt thereof.
- fullerene of the invention of this application may be C 60 fullerene, C 70 fullerene or nanotube fullerene, or a mixture of one or more selected from them.
- the fullerene in which a car pump rack (a soot containing a fullerene) as a fullerene powder product remains may be used as long as the concentration of carbon black in the fullerene is 0 to 98% by weight.
- the fullerenes of the invention of this application include various substituents in such a carbon skeleton structure, for example, a hydrocarbon group, an oxygen crosslinking group, a hydroxyl group, an acyl group, an ether, which may have a substituent. Also included are fullerene derivatives having an oxygen-containing group such as a group, a strong lpoxyl group, a nitrogen-containing group such as an amino group or a cyan group.
- fullerene oxygen-containing derivative one in which an oxygen atom is bonded directly to a carbon atom of a fullerene skeleton or via a carbon chain such as an alkylene chain is considered.
- fullerene hydroxide having a direct bonding of —OH groups up to a hydroxylation rate of about 50 / mol fullerene.
- fullerenes that can be used in the present invention, fullerenes represented by the following chemical formulas can be used.
- R im is m substituents bonded to Cn, each independently or independently of a hydroxyl group, an ester group of the hydroxyl group and an inorganic acid or an organic acid, It represents a glycoside group of a hydroxyl group and a sugar, a ketal group of the hydroxyl group and a ketone, or an acetal group of the hydroxyl group and an aldehyde.
- R 2m is m atoms bonded to Cn, and each independently represents the same or different, or one atom bonded to two or more different carbons. m represents 0 or an integer of 1 or more.
- the fullerenes that can be used in the present invention are one or more simple substances or mixtures selected from fullerene multimers, force-bonnanotubes, derivatives thereof, and salts thereof, and organication that modifies or includes them. A compound may be used.
- fullerene multimers include those represented by the following formula. That is, put Komatsu et groups cyanide and flour ⁇ iron ball of Kyoto force capsule steel was successfully synthesized giving fast vibration per minute 3500 times, dimer C 60 (C I2Q;) , And trimers (C 180, below), C 62 synthesized by Rubin et al., Fullerene nitrogen atom synthesized by Wudl et al. (C 59 N) 2 , etc.
- fullerene derivatives that can be used in the present invention include C 6D F and C 6D F 18 in which fluorine is allowed to act on fullerene.
- the present invention also includes a metal-encapsulated fullerene (M in the formula represents a metal atom) as shown below, for example, which is synthesized by mixing a metal in the powder of grapheye koji and evaporating it by applying a laser. Can be used.
- M in the formula represents a metal atom
- Specific examples of the metal-encapsulated fullerene that can be used in the present invention include, but are not limited to, scandium, lanthanum, cesium, and titanium-encapsulated fullerene.
- Metal-encapsulated fullerenes ( ⁇ c 60 ) As the fullerenes that can be used in the present invention, for example, atomic-encapsulated fullerenes (the small spheres in the formulas indicate atoms) as shown below.
- fullerenes that can be used in the present invention are selected from fullerene cleavage products, fullerene cleavage products, derivatives thereof and salts thereof.
- cleavage fullerenes examples include open cage fullerenes produced by RuMn et al. And perforated fullerenes synthesized by Komatsu et al.
- the fullerenes that can be used in the present invention include complexes with organic compounds that modify, include, or complex fullerenes.
- organic compound an organic oligomer, an organic polymer, and an inclusion compound or an inclusion compound or a cyclodextrin (CD) capable of forming an inclusion complex, a crown ether, or one or more of those related compounds are suitable. As illustrated.
- organic oligomers and organic polymers include carboxylic acid esters, alcohols, saccharides, polysaccharides, polyhydric alcohols, and polyethylene.
- Polymers of polyalkylene dallicol or polyhydric alcohols such as polyglycol, butylene glycol, polypropylene glycol, polyvinyl alcohol, etc., starch derivatives such as dextran, pullulan, starch, hydroxyethyl starch and hydroxypropyl starch
- Nonionic water-soluble polymers containing alginic acid, hyaluronic acid, chitosan, chitin derivatives, and anionic or cationic derivatives of these polymers and these polymers glycerin and fatty acids, oils, propylene carbonate, Lauryl alcohol, ethoxylated castor oil, polysorbates, and esters or ethers thereof, polymers thereof, polyester polymers thereof, pyrrolidone polymers such as polyvinylpyrrolidone, etc.
- No Saturated alcohol polymers such as esters or ethers and polyoxyethylenepolypropylene block copolymers are preferably bonded to fullerene or a derivative thereof, and may be a mixture of one or more of them.
- various things such as polyalkylene glycols, such as polyethyleneglycol (PEG), polyvinyl pyrrolidone (PVP), are illustrated as a preferable thing.
- PEG polyethyleneglycol
- PVP polyvinyl pyrrolidone
- the average molecular weight is generally preferably about 200 to 100
- the ratio with the fullerene or fullerene-containing oxygen derivative is preferably It is considered that the molar ratio is about 10/1 or less.
- fullerene salts of the invention of this application are selected from, for example, hydroxylated fullerenes, salts of fullerene esters, polyhydroxylated fullerenes, fullerene range esters, fullerene triesters, fullerene polyesters and the like. Often, the salts only need to form physiologically acceptable salts. Examples of these salts include inorganic salts and organic salts.
- These salts include alkali metals (eg, sodium, potassium, etc.) and alkaline earth metals (eg, calcium, magnesium, etc.) Or a salt with an organic base such as trimethylamine, triethylamine, pyridine, picoline, N, N-dibenzylethylenediamine, ethanolamine, diethanolamine, trishydroxymethylaminomethane, dicyclohexylamine, etc. There may be. From the viewpoints of high safety and economy, one or more metal salts selected from sodium, potassium, magnesium, calcium, and aluminum are suitable as the salts of hydroxylated fullerenes and fullerene monoesters. is doing.
- fullerenes that can be used in the present invention include, for example, cyclodextrin as shown in the following formula, porphyrin complex (Jaws porphyrin) synthesized by Boyd et al., Double nanoring cyclophanefullerene complex, Nakamura et al. Also included are fullerene-phenolate derivatives, fullerene-phenyl derivatives Ph 5 C 6 () , fullerene-biphenyl derivatives, etc. Fullerene derivatives that are water-soluble as fullerenes, modified or clathrates with organic compounds, and fullerene salts are highly stable, easily soluble in water, and have an adjustable pH, resulting in low cytotoxicity.
- porphyrin complex Jaws porphyrin
- Double nanoring cyclophanefullerene complex Nakamura et al.
- fullerene-phenolate derivatives fullerene-phenyl derivatives Ph 5 C 6 ()
- fullerenes and polymeric polymers such as PEG (polyethylene glycol), PVP (polovinylpyrrolidone), or modified with CD (cyclodextrin) or inclusion bodies, and monovalent salts are more water-soluble than divalent salts. It is preferable because of its high solubility in water.
- fullerene-PVP, sodium fullerene hydroxide and sodium fullerene esters, and full power of fullerene hydroxide and monoesters are suitable.
- PVP polyvinylpyrrolidone
- the weight average molecular weight (Mw) is in the range of about 3, 00 to 3, 0 0 0, 0 0 0, , 0 0 0 to 1, 5 0 0, 0 0 0 or so are considered to be suitable.
- PVP may be a synthesized product or a commercially available product.
- the fullerene in this case may be a fullerene derivative as described above.
- fullerenes that can be used in the present invention include, for example, cyclodextrin as shown in the following formula, porphyrin complex (Jaws porphyrin) synthesized by Boyd et al., Double nanoring cyclophanefullerene complex, etc. Also included are fullerene-one-phucene derivatives synthesized by Nakamura et al., Fullerene-phenyl derivatives Ph 5 , fullerene-biphenyl derivatives, and the like.
- porphyrin complex Jaws porphyrin
- Double nanoring cyclophanefullerene complex etc.
- fullerene-one-phucene derivatives synthesized by Nakamura et al.
- Fullerene-phenyl derivatives Ph 5 fullerene-biphenyl derivatives, and the like.
- fullerene cyclodexporin inclusion bodies include those in which an oxygen atom is bonded directly to a carbon atom of a fullerene skeleton or via a carbon chain such as an alkylene chain.
- fullerene hydroxide having a hydroxylation rate of 50 nomole fullerene or more and one OH group directly bonded thereto is exemplified.
- the fullerene cleaved body or fragment that can be used in the present invention may be a fullerene cleaved body or split body represented by the following chemical formula, or a simple substance or a complex of a molecule containing the structure.
- C is a fullerene partial structure represented by a carbon atom, and it is sufficient that two or more carbon atoms are covalently bonded (if there is a carbon that is not covalently bonded, R n Even if there is no display of, R n R n is n substituents bonded to C, each independently or independently, a hydrogen atom, a carbon atom, an oxygen atom, a nitrogen atom, a phosphorus atom, a hydroxyl group, It represents an ester group of the hydroxyl group and an inorganic acid or an organic acid, a glycoside group of the hydroxyl group and a sugar, a ketal group of the hydroxyl group and a ketone, or an acetal group of the hydroxyl group and an aldehyde.
- n represents an integer of 0 or 1 or more.
- examples of the split fullerene that can be used in the present invention include corannulene (C 20 H 10 ) having a C 60 fullerene fragment structure as shown in the following formula.
- a long-chain carboxylic acid having 10 or more carbon atoms, or an ester or salt thereof is also effective to contain a long-chain carboxylic acid having 10 or more carbon atoms, or an ester or salt thereof, together with the above-mentioned active ingredients and fullerenes as useful ingredients.
- oil agents, surfactants, pigments, humectants, excipients and bases, cell activators, and the like as described below may be blended.
- the pH varies depending on the pH of the fullerene, the fullerene derivative, the fullerene clathrate compound, or a salt thereof, but usually the pH is 3 to 10 If it is in this range, fullerene and its derivatives can be blended stably, which is preferable.
- ⁇ is the rounded number of pH of a 0.5% by weight aqueous solution of 20 of the fullerene, fullerene derivative, fullerene-modified or clathrate compound, or salt thereof, and ⁇ is 3
- the pH of a stable fullerene topical preparation should be in the range of 3 to 4, and if the pH of ⁇ is 10 or more, it should be pH 9 to 10.
- the pH of the stable fullerene-containing external composition is preferably in the range of 3 to 10.
- free radical diseases include myocardial infarction, ischemic heart disease, heart failure, angina pectoris, arrhythmia, arteriosclerosis, liver lipid metabolism disorder, hyperlipidemia, essential hypertension, hypertension, arteriosclerosis, Coronary sclerosis, thrombosis, obstructive arteriosclerosis, vascular disorder, peripheral blood vessel disorder, cholestasis, hypercholesterolemia, knee disorder, organ failure, acute chronic hepatitis, gastric ulcer, duodenal ulcer, ulcerative colitis Digestive organ disorder, cholecystosis, diabetes, arthritis treatment, rheumatism, liver failure, liver disorder, ischemic liver disorder, liver lipid metabolism disorder, gallbladder disorder, organ transplant disorder, diabetes, poisoning, organ transplant disorder, Cancer, ischemic reperfusion injury
- the composition for preventing and treating free radical disease of the present invention is a mammal (for example, mouse, rat, pig, raccoon dog, fox, cat, rabbit, rabbit, cinnamon) that retains cancer (tumor). , Horses, goats, monkeys, humans), and is effective in prolonging the life of these cancer-bearing animals and suppressing cancer metastasis.
- the cancer to which the free radical disease preventive treatment composition of the present invention is applied includes a tumor, a benign tumor, or a malignant tumor.
- malignant melanoma malignant lymphoma, digestive organ cancer, lung cancer, esophageal cancer, stomach cancer, large intestine cancer, rectal cancer, colon cancer, ureteral tumor, gallbladder cancer, bile duct cancer, biliary tract cancer, breast cancer, liver cancer, knee Visceral cancer, testicular cancer, maxillary cancer, tongue cancer, lip cancer, oral cancer, pharyngeal cancer, laryngeal cancer, ovarian cancer, uterine cancer, prostate cancer, thyroid cancer, brain tumor, force positive sarcoma, hemangioma, leukemia, genuine Also included are polycythemia, neuroblastoma, retinoblastoma, myeloma, cystoma, sarcoma, osteosarcoma, myoma, skin cancer, basal cell cancer, skin appendage cancer, skin metastasis cancer, skin There are also melanomas.
- the composition for preventing and treating free radical disease of the present invention also exerts the effects of cancer treatment and cancer prevention (including metastasis inhibition). Therefore, by further containing one or more antitumor agents, Furthermore, it can enhance the effects of cancer treatment and cancer prevention (including metastasis inhibition).
- this antitumor agent examples include nitromin (R), cyclophosphamide, melphalan, thiotepa, force lupocon, Protecton (R), busulfan, dimustine hydrochloride, mitopuritol, ifosfamide, mercaptopurine, Thioinosine, Shibu Rabin, Dagarvadine, Fluorouracil, Tegafur, Ancitabine hydrochloride, Methotrexate, Carmofur, UFT (R), Enoshiba bin, Bin plastin sulfate, Vincristine sulfate, Vindesine sulfate, Lactinomycin (D), Mitomycin ( :, Chromomycin A3, bleomycin hydrochloride, bleomycin sulfate, daunorubicin hydrochloride, doxorubicin hydrochloride, neocartinostatin, beptibromycin sulfate, a
- the anticancer effect of cancer transfer can be enhanced even when an anticancer agent such as Inferon Ferron obtained by a natural type or genetic engineering technique is used in combination with the active ingredient of the present invention.
- ischemic reperfusion injury which is an application of the composition for preventing and treating free radical disease of the present invention, specifically includes ischemic heart disease, ischemic reperfusion myocardial injury, ischemic liver injury, ischemic Reperfusion liver disorder, ischemic reperfusion kidney disorder, ischemic reperfusion spleen disorder, ischemic reperfusion gallbladder disorder, ischemic reperfusion cardiovascular disorder, ischemic reperfusion gastrointestinal disorder, ischemic reperfusion myopathy There are ischemic reperfusion vascular disorder, ischemic reperfusion ocular disorder, ischemic reperfusion skin disorder.
- infectious diseases to which the composition for preventing and treating free radical disease of the present invention is applied include bacterial infections such as enteric bacterial infections caused by Escherichia coli, hepatitis due to hepatitis virus, acquired immune deficiency syndrome due to HIV (AI DS), colds caused by rhinoviruses, influenza infections caused by influenza viruses, fungal infections such as candidiasis caused by Candida fungi, and parasitic infections such as malaria caused by malaria parasites.
- bacterial infections such as enteric bacterial infections caused by Escherichia coli, hepatitis due to hepatitis virus, acquired immune deficiency syndrome due to HIV (AI DS), colds caused by rhinoviruses, influenza infections caused by influenza viruses, fungal infections such as candidiasis caused by Candida fungi, and parasitic infections such as malaria caused by malaria parasites.
- other free radical diseases that are targets of the composition for preventing and treating free radical diseases of the present invention include vascular thrombosis, anemia, ischemia, and vascular sclerosis associated with the above organs of the present invention.
- Vasoconstriction Vasoconstriction, blood flow rate (OBAYASH I, PROC. SOC. EXP. BI OL. WED., 1 9 6, 1 9 6, 1 64-1 6 9, 1 9 90) etc.
- OBAYASH I PROC. SOC. EXP. BI OL. WED., 1 9 6, 1 9 6, 1 64-1 6 9, 1 9 90
- Examples include, but are also effective for, damage to cells and tissues associated with physical deterioration and cessation of the disease, illness and disease and insufficiency of organs including blood vessels.
- free radical diseases targeted by the composition for preventing and treating free radical diseases of the present invention include oxygen deficiency caused by a decrease in oxygen pressure in blood vessels and chemicals such as pesticides and carbon monoxide poisoning. It can also include temporary oxygen deficiency of tissue or oxygen deficiency of tissues due to substances, and is sent to cells or tissues with normal or close blood flow by appropriate treatment or event such as blood transfusion. Examples include damage to cells and tissues that are found at the time of detection, disease and insufficiency of organs including blood vessels and blood vessels, and these are also effective.
- the composition for preventing and treating free radical disease of the present invention is particularly effective, and is a specific example of the ischemic reperfusion disease of the free radical disease to be targeted.
- Examples include ischemia-reperfusion myocardial injury (NAR I TA. W. J, J. LAB. CL I N. MED., 1 1 0, 1 5 3— 1 5 8, 1 9 8 7, Sm ith, L. L. Phil.Trans.R.Soc.Lond., 3 1 1, 6
- VIER VIER
- AM S TERDAM 1 9 9 0, Nakahama, Liver, 32: 1 1 1 1 0-1 1 2 3, 1 9 9 1, Takekawa, Liver, 3 0: 4 5 9— 4 67, 1 9 8 9, Shirasugi, Nissho Gaijin, 2 6: 3 5 8, 1 9 9 3) Ischemia-reperfusion kidney injury, ischemia-reperfusion knee injury (ISAJI, S .: MIE MED. J., 3 5: 1 09-1 2 3, 1 98 5), ischemic reperfusion gallbladder disorder (TAOKA, GAS TROENT.
- JP N., 2 6: 6 3 3-644, 1 9 9 1) ischemic reperfusion circulatory system Disorders, ischemia-reperfusion digestive disorders (Iwai, Nisshokai, 87: 1 6 6 2-1 6 6 9, 1 990, NA I TO, Y., FREE RED. RE
- composition for preventing and treating free radical disease of the present invention is also effective for the following various disorders induced by active oxygen.
- Specific examples include Behcet's disease, radiation damage, side effects of anticancer drugs, bacterial shock, cachexia, autoimmune disease, burns, herpes virus, adult T cell leukemia, thioredoxin syndrome, traumatic shock, Examples include fungal amyotrophic lateral sclerosis and asexual myocardial infarction.
- the composition for preventing and treating free radical disease of the present invention has low toxicity and can be administered orally or parenterally to a mammal containing human.
- the composition for preventing and treating free radical disease of the present invention is not particularly limited, and is an oral administration agent, an infusion solution, a tablet, a powder, a liquid suppository, an external preparation, an ointment, a patch, an eye drop, an intravenous injection, a powder, Granules, tablets, dragees, capsules, pills, Suspensions, liquids, ampoules, injection solutions, isotonic solutions, etc. can be mentioned, and they can be applied to other forms of pharmaceutical products.
- the main active ingredients are fullerenes: cyclodextrin-containing C 60 fullerene, hydroxylation rate of 50 / mol ⁇ fullerene or more — hydroxylated hydroxyl group with directly bonded OH groups C 60 and C 70 fullerene
- the metal salt include sodium salt, potassium salt, calcium salt, and magnesium salt.
- It can be formulated as a pharmaceutically acceptable inert carrier or as a mixture with diluted opium or other pharmacological agents, or in dosage unit form.
- the main component of the present invention may be used as a cyclodextrin or a complex with maltocycle cyclodextrin for the purpose of increasing solubility in water to promote absorption and enhancing pharmacological activity.
- composition for preventing and treating free radical disease of the present invention is usually used orally or parenterally as a pharmaceutical composition comprising these active ingredients mixed with a pharmacologically acceptable carrier or excipient. It is done.
- each active ingredient is made into an aqueous solution beforehand, each active ingredient is freeze-dried to form a solid mixture, and each active ingredient made into an aqueous solution is freeze-dried to make each solid form.
- One of the active ingredients is an aqueous solution and another active ingredient is freeze-dried to form a solid form, and the form of a kit or the like in which each active ingredient is separately formulated.
- the present invention was listed in the twelfth revised Japanese Pharmacopoeia Heisei 3 (Shishin Shoten), etc., which can be pharmaceutically acceptable if desired according to known pharmaceutical manufacturing methods. Diluents, excipients, etc. can be mixed and administered as a single agent.
- each active ingredient can be pharmaceutically acceptable if desired. It is also possible to formulate it using a diluent, excipient, etc., and administer it as a single agent using a working diluent. Furthermore, as described above, a separate formulation is used as a kit, and these are administered separately, at the same time, or with a time difference, to the same subject by the same route or different routes. It can also be.
- composition of the present invention is a solution
- a water-soluble agent for example, distilled water
- a water-soluble preparation for example, physiological saline, Ringer's solution, etc.
- an oily solvent for example, sesame oil, corn oil
- Olive oil etc.
- a solubilizer eg, sodium salicylate, sodium acetate, etc.
- a buffer eg, sodium citrate, glycerin, etc.
- an isotonic agent eg, sugar, etc.
- a stabilizer eg, sugar
- Additives such as human serum albumin, polyethylene glycol, etc.), preservatives (eg, benzyl alcohol, phenol, etc.), soothing agents (eg, benzalkonium chloride, pro-in hydrochloride, etc.) can also be used.
- Pharmacologically and pharmaceutically acceptable additives as desired e.g. diluents, excipients, binders, disintegrants, colorants, stabilizers, extenders, wetting agents, surfactants, lubricants
- a mixture of a mixture, a dispersant, a buffering agent, a buffering agent, a flavoring agent, a flavoring agent, a flavoring agent, a preservative, a solubilizing agent, a solvent, a coating agent, a sugar coating agent, etc. it can.
- the diluent used for the preparation of the composition for preventing and treating free radical disease of the present invention is pharmaceutically acceptable, but means a material other than the inventive compound of this application, and is solid, semi-solid, liquid or ingested. Capsules that can be used may be used, and various types of capsules can be used.
- the composition for preventing and treating free radical disease obtained by the present invention may be produced by any known method.
- the active ingredient is mixed with a diluent, for example, into granules, and then the composition is prepared. It can also be formed into tablets, for example.
- Parenteral preparations should be sterile and, if necessary, isotonic with blood. Parenteral administration includes administration by injection (including, for example, intramuscular intravenous infusion) and transanal (suppository).
- composition of the present invention itself can be a cancer metastasis inhibitor, fullerenes or salts thereof which are active ingredients in preparations and compositions are generally used.
- compositions for oral administration further include tablets, pills, granules, powders, capsules, syrups, emulsions, suspensions, and sprays.
- Such a composition is produced by a method known per se, and lactose, starch, sucrose, steamonoester magnesium and the like are used as a carrier or an excipient.
- injections, suppositories, patches, eye drops, external preparations, etc. can be used, for example, intravenous infusions, subdermal injections, intramuscular injections It is used as a drug and infusion.
- the injection is usually provided in a suitable ampoule.
- dosage forms include rectal suppositories and vaginal suppositories
- external preparations include ointments, nasal injections, and transdermal preparations.
- the composition of the invention of this application can be made into a solid, semi-solid or liquid external preparation according to a method known per se.
- the composition of the invention of this application is used as it is or an excipient (eg, glycol, mannitol, starch, microcrystal, cellulose, etc.), a thickener (eg, natural) Gums, cellulose derivatives, acrylic polymers, etc.) are added and mixed to obtain a powdery composition.
- an excipient eg, glycol, mannitol, starch, microcrystal, cellulose, etc.
- a thickener eg, natural Gums, cellulose derivatives, acrylic polymers, etc.
- liquids are almost the same as in the case of injections, and should be oily or aqueous suspensions.
- an aqueous or oily gel or an ointment is preferred.
- pH regulators eg, carbonic acid, monoester, citrate, hydrochloric acid, sodium hydroxide, etc.
- preservatives eg, paraoxybenzoate
- Perfume esters, chlorobutanol, benzalkonium chloride, etc. may be added.
- the composition of the invention of this application can be made into an oily or aqueous solid, semisolid or liquid suppository.
- the concentration of fullerenes to be blended in the composition of the present invention is 0.001 to 100 ppm based on the total weight of the composition for preventing and treating free radical diseases of the present invention. In view of good solubility in blood, 0.1 to: I 0 0 ⁇ ⁇ m is preferable.
- substances that can be incorporated into the composition for preventing and treating free radical diseases of the present invention for the purpose of stabilizers, active active agents and the like include metolazol, etopside, cholic acids, dimethylsulfol, which are generally used as additives.
- Water-soluble polymer compounds such as cisids, adesosine phosphates, polyethylene glycols, polypropylene glycols, inorganic salts such as sodium chloride, chlorinated lithium, magnesium chloride, citrate, malic acid, phosphoric acid, edetic acid, Selected from organic acids such as oxalic acid, lactic acid, butyric acid, acetic acid, ascorbic acid, erythorbic acid, sialic acid and amino acids and their organic acid salts, or polyhydric alcohols such as propylene glycol, butylene glycol and glycerin One or a mixture of two or more may be mentioned.
- the cholic acids are selected from bile acids, dehydrocholic acids, deoxycholic acids or their alkaline earth metal salts such as sodium and potassium.
- the adenosine phosphate is selected from adenosine phosphates such as adenosine mono5′3 phosphate, adenosine mono5′2 phosphate, and adenylate.
- oral preparations, external preparations and injection preparations are desirable from the viewpoint of simplicity of administration and effects.
- the drug of the present invention can be formulated by combining the above pure substance or a mixture thereof with a known pharmaceutical carrier, and has the highest effect and is easy to administer. Is preferred.
- a fullerene water adduct or a crystal water adduct is an anhydride thereof. It is useful because it has a higher solubility in water.
- the water content or water content of the fullerenes or crystal water adducts of the present invention is not particularly limited, but in order to maintain better solubility, the water content is 1% to 50% by weight, More preferably 5% to 20% by weight, and in the case of crystal water, a water adduct or crystal water adduct of fullerenes holding water molecules in the range of 1 to 20 hydrates, more preferably 1 to 10 hydrates is desirable. .
- the dosage of fullerenes of the present invention will be described. Although it varies depending on symptoms, age, sex, body weight, dosage form, dosage form, for example, oral administration, suppository administration, external preparation, etc. 0.001 to 8500 mg per kg. Preferably in the range of l-100 mg. In addition, in the case of intravenous injection or infusion, it is usually possible to administer 0.025 to 200 mg, preferably 0.25 to 100 mg, in 1 or several divided doses per body weight per day for an adult.
- the injection of the present invention is intravenously or instilled into a vein or the like at 0.1 to 50 cc per kg of human body weight so that the total amount of dissolved substances in the injection solution is 1 gZkg / hour or less.
- the dose of fullerenes of the present invention varies depending on the preparation type and administration method. Usually, 1 / mgZkg body weight / day to lOmg / kg body weight Zday is administered once or divided into several times.
- composition for the prevention and treatment of free radical disease of the present invention may be added by adjusting the kind and amount of the fullerenes and cleavage fullerenes and derivative salts thereof of the present invention, or the fullerenes of the present invention.
- an additive capable of adjusting the osmotic pressure to the cleaved fullerenes and their derivative salts, the permeability of fullerenes, cleaved fullerenes and their derivative salts, which are the main components of the solution, to tissue cells is increased. A greater effect can be obtained.
- Additives that can adjust the osmotic pressure include inorganic salts such as sodium chloride and potassium chloride, organic acids such as ATP, malic acid and citrate or organic acid salts such as sodium, sugars such as glucose and fructose, etc.
- inorganic salts such as sodium chloride and potassium chloride
- organic acids such as ATP, malic acid and citrate or organic acid salts such as sodium
- sugars such as glucose and fructose, etc.
- physiologically acceptable additive such as one or two or more composites selected from the above.
- Antioxidants include vitamin B, L-ascorbic acid, tocopherol, and L-ascorbic acid-2-phosphoric acid and other saccharoses such as L-ascorbic acid, ubiquinone, uric acid, cystis , Dalyuthione, Dalthathione Peroxylase, SOD, Quenic Acids, Phosphoric Acids, Polyphenols, Sodium Bisulfite, Sodium Bisulfite, Erythorbic Acid, Sodium Erythorbate, Dilauryl Thiodipropioate, Kotocoli Enol, Lipoic acid, Trilbiguanide, Nordihydroguaiaretinic acid, Parahydroxylanisol, Ptylhydroxanisol, Dibutylhydroxytoluene, Ascorbyl stearate, Ascorbyl palmitate, Octyl gallate,
- Fullerenes which are the active ingredients of the composition for preventing and treating free radical diseases of the present invention, inhibit and stabilize such antioxidants, particularly ascorbic acid, at the time of production, storage period, digestion. There is little degradation over time in the tube. In addition, when normal ascorbic acid is taken into the living body, it is degraded by radicals contained in the living body, particularly food in the digestive tract, etc., and is hydrolyzed and deactivated before reaching the target cell. Fullerenes, which are active ingredients, are stable and are absorbed by the body through nutrient-absorbing cells without being inactivated.
- fullerenes exhibit extremely high cell absorbability.
- the concentration of intracellular ascorbic acid can be increased up to about 30 times as compared with fullerene and about twice as high as that of ascorbic acid.
- the composition for preventing and treating free radical disease of the present invention can exert the cancer metastasis inhibitory action that is not recognized by ascorbic acid as described above.
- cancer cells Because of its dynamic performance, cancer cells can invade blood vessels from the lesion and migrate to a wide range of organs and proliferate. For this reason, the life extension period is remarkably shortened.
- the anti-tumor action of the fullerenes of the present invention can exert a cancer metastasis inhibitory action, particularly by inhibiting the ability of cancer cells to migrate from the lesion to the vascular endothelium and consequently inhibiting cancer metastasis. It has been confirmed. It has been found that cancer cells administered with the fullerenes of the invention of this application show a very low infiltration rate into the vascular endothelium. This action has been confirmed to be unique to fullerenes.
- fullerenes which are active ingredients of the composition for preventing and treating free radical disease of the present invention, inhibit and stabilize oxidative degradation of ascorbic acid.
- fullerenes exhibit extremely high cell absorptivity and can efficiently increase intracellular ascorbic acid concentration, so that the antitumor action of ascorbic acid can be maximized.
- the antitumor action of fullerenes is thought to exert its anticancer action, particularly by inhibiting the invasion of tumor cells into the vascular endothelium and consequently inhibiting cancer metastasis.
- the composition for preventing and treating free radical diseases of the present invention can be applied to pharmaceuticals, quasi drugs, cosmetics, and functional foods.
- the composition of the present invention can take all dosage forms such as powders, liquids, tablets, gels, emulsions, capsules, etc., specifically, drinks, injections, ointments, suppositories, external preparations. Can be applied. More specifically, it can be used as products such as lotions, milk lotions, creams, packs, shampoos, rinses, hair restorers, hair nourishing agents, hair dyes, hair conditioners, scouring, gargles, bathing agents, etc. It is not particularly limited.
- Cosmetics in the present invention include, for example, makeup cosmetics such as foundation, white powder, wisdom shadow, eyeliner, eyebrow, teak, lipstick, nail color, etc .; emulsion, cream, lotion, calamine lotion, sunscreen agent, suntan agent, After shave lotion, Basic cosmetics such as sachets, rinses, conditioners, hair colors, hair tonics, set agents, hair nourishing agents, permanent agents, etc .; pode powder, It is classified into deodorant, hair remover, seggen, body shampoo, bath preparation, hand soap, perfume, etc. and can be used as cosmetics for each.
- the dosage form of the present invention is not particularly limited, and is conventionally known such as a two-layered, water-in-oil emulsion, oil-in-water emulsion, jewel, spray, mousse, oil, solid, sheet, powder, etc.
- the dosage form can be used.
- the present invention comprises a fullerene having high radical scavenging activity in vivo as an active ingredient as a main component, so that it is stable during preparation and storage, and is safe and effective with few side effects on the living body. It was possible to provide a composition for preventing and treating free radical diseases.
- the solution was sterilized and filtered through a sterilizing filter for producing injection solution, and an injection solution was produced as a preventive / remedy for intravenous free radical disease of the present invention.
- Hydroxylation rate 8 7% (mol conversion) C 60 Fullerene and hydroxylation rate 6 1% (molar equivalent) of hydroxylated C 70 fullerene uniformly mixed at a weight ratio of 8: 2 was completely dissolved in 10 cc cc pharmaceutical Ringer's solution at a concentration of 5 ppm and then injected. Sterile filtration was performed with a sterilizing filter for liquid production, and an injection solution was produced as a free radical disease preventive / remedy for intravenous injection according to the present invention.
- Example 5 Water-soluble external preparation and cosmetic lotion
- Example 1 of the present invention was intravenously administered to rats, and as a control group, only Ringer's solution was injected in the same manner as in the test group.
- free radical-dependent chemiluminescence in peripheral blood was measured by chemiluminescence before the experiment, a significant increase in free radicals was confirmed immediately after reperfusion.
- Rat crown as test area in advance Arterial block 1 5 mg / kg of the free radical disease prevention and treatment composition of the present invention, which is 5 mg / kg, is administered intravenously to rats as a control group, and only Ringer's solution is used as a control group in the same manner as in the test group. Injected into.
- the blood amylase level in the control group was significantly higher than the level before blocking, and up to 60 00 U / dl individuals were observed.
- the blood amylase level in the test group to which the injection of the present invention was administered was 100 0 U / d 1 at the maximum, and a slight amylase increased tendency was observed compared to the normal state before blockade. However, it was significantly lower than the control group, and the effect of the composition for preventing and treating free radical disease of the present invention on the knee disease was proved.
- Example 4 After blocking the rat coronary artery for 20 minutes and resuming blood flow for 60 minutes, a renal disease model that damaged the kidney tissue was created, and the mean urinary protein was measured before coronary artery blockage and after resumption of blood flow for 5 days did.
- free radical-dependent chemiluminescence in peripheral blood was measured by chemical luminescence before the experiment, a significant increase in free radicals was confirmed immediately after resumption of blood flow.
- 5 mkg of the injection of Example 4 was intravenously administered to the rat 15 minutes before blockage of the rat coronary artery, and only Ringer's solution was injected as a control group in the same manner as the test group.
- the urinary protein level in the control group was significantly higher than the level before the blockade, and the renal disease was clearly observed.
- the urinary protein level in the administered test group showed a slight increase in urinary protein compared to the normal state before blocking, but it was significantly lower than that in the control group.
- the cell necrosis index of the heart, liver, kidney, knee and gallbladder is 45 C. a Obtained by autoradiograph image analyzer.
- the cell necrosis index of the heart, liver, kidney, knee and gallbladder is 45 C. a Obtained by autoradiograph image analyzer.
- In the control rats delayed cell death in which many cells were necrotized in each organ after ischemia was observed, but in the mice injected with the injection of the present invention (10 mice per group), necrosis of each cell was observed. Has been confirmed to be remarkably prevented.
- the same amount of the pharmaceutical composition of the present invention was injected once a day for 5 days, dissected after 10 days, and the cell necrosis index of the heart, liver, kidney, knee and gallbladder was determined as 45. It was determined by C a autoradiography / image analyzer. In the control rats, when seen with a 45 Ca autoradiography image analyzer, delayed cell death in which many cells were killed in each organ after ischemia was observed, but the injection solution of the present invention was injected. In mice (8 mice per group), it was confirmed that the death of each cell was remarkably prevented.
- Skin diseases that are said to involve free radicals, pigmentation due to sunlight, skin folds, alveolar pyorrhea in the oral cavity, seborrhea of skin tissue, acne, Males and females suffering from hair loss 5 1 3 out of 3 2 2 4 Only mannitol as a control group and the remaining 2 8 9 patients as a test group
- the water-soluble external preparation of Example 5 was used in the morning and evening 2 times a day, 5 cc (—l O cc per day) was applied for 3 months or only in the case of alveolar pyorrhea, and the mouth was rinsed for 3 minutes with mouthwash and the symptoms were recorded every other week.
- M i 1 1 1 i-Q registered trademark
- fullerene polyester two hydroxylations of fullerene hydroxide are esterified with acetic acid, and for Na and Na-K salts, two hydroxyl groups are esterified with acetic acid. These two hydroxyl groups were substituted with Na or Na and K.
- the powders of the present invention were produced by mixing and pulverizing with the formulation (% by weight) shown in Table 3.
- Sterilized compounds listed in Table 1 (Prescription Nos. 1 to 10) 1 g each is aseptically dissolved in 5% glucose solution for injection to 10 Om 1, filtered through a 0.2 tm membrane filter, and 10 ml injected An injection was obtained by filling the ampoule.
- Sterilized compounds shown in Table 1 above (Formulation Nos. 1 to 10) 5 g each and 5% glucose solution for infusion 500 ml 1 were dissolved, followed by filtration through a 0.2 mm membrane filter to obtain an infusion solution.
- a powder was obtained by mixing 1 g of each of the compounds described in Table 1 (prescription numbers 1 to 10) and 10 g of crystalline lactose.
- Oral syrups were obtained by suspending the compounds described in Table 1 (prescription numbers 1 to 10) in an oral syrup solution.
- An external preparation (ointment) of the composition for the prevention and treatment of free radical disease of the present invention was produced by a conventional method according to the prescription in Table 5 below.
- liquid preparation for the free radical disease prevention / treatment composition of the invention of this application was produced by a conventional method.
- PVP Fullerene (P VP molecular weight 60, 000) 5. 0 Methyl paraoxybenzoate 0.1 Sodium citrate 0. 5 Quenic acid 0. 05
- Test example 1 Stability test
- PVP .fullerene PVP molecular weight 60, 000
- fullerene mono Table 7 shows the difference in stability between esters and fullerene monoester salts in aqueous solution (10-day room temperature storage test). It can be seen that fullerenes are stable regardless of the type, but ascorbic acid is easily hydrolyzed in purified water over time.
- the stability was evaluated by allowing a 0.1% aqueous solution (purified water) of the above substance to stand at room temperature for 10 days and measuring the residual ratio by HPLC.
- Test example 2 Intracellular absorbability (intracellular transport) test
- Test example 3 Cell mobility (cell tactility) test
- the cancer cells were preliminarily administered with ascorbic acid for 18 hours, and the fullerenes of the invention of this application having prescription numbers 1 to 13 in Table 1 above.
- the number of infiltrating cancer cells in the case of no administration was 12400, but in any case, the number decreased significantly.
- PVP ⁇ fullerene PVP molecular weight 60,000
- Rats spontaneous breast cancer cells were implanted subcutaneously in the back of spontaneously hypertensive rats (S HR rats) (5 rats per group), and the rats were sacrificed 35 days later. The number of lung weights and the number of colonies formed was measured, and the degree of lung metastasis of SST-2 was observed.
- the compound administration group of the invention of this application of prescription No. 1 in Table 1 above is 50 and from 7 days before transplantation to 34 days after transplantation.
- W 10 Omg / rat was orally administered and injected subcutaneously, and subcutaneous tumor weight, lung weight, and number of metastatic colonies were compared with the untreated control group. The results are shown in Table 8.
- the compound administration group of the present invention has an action of suppressing metastasis to the lung.
- Rats spontaneous breast cancer cells (S ST-2) were transplanted subcutaneously in the back of spontaneously hypertensive rats (S HR rats) (5 rats in each group) 1 X 1 0 0, 0 0 0 cells 3 5 days Later, the rats were sacrificed to determine the number of lung weights and colony formation, and the degree of lung metastasis of SST-2 was observed.
- the compound administration group of the invention of this application of prescription No. 1 in Table 1 above was tested for carrier administration and combined administration with known anticancer agents shown in Table 9. From the 7th day before transplantation to the 34th day after transplantation, the compound of the invention of this application 5 Omg / day / rat.
- Test Example 6 Evaluation of inhibitory effect on mouse skin cancer metastasis
- PVP * fullerene P VP molecular weight 60, 0 00
- the cancer wetness test was conducted using 2 ml). In the test, P VP fullerene was administered immediately before cancer cells infiltrated into the reconstituted basement membrane, and PVP fullerene was administered 1 hour before cancer cells infiltrated into the reconstituted basement membrane. Then, the cells were gently agitated for 1 hour to prevent cell adhesion, and were then infiltrated with “pretreatment hr”.
- Matrigel (0.1 2 mg / m 1) 40 ⁇ , I was used. Compared to the case of non-administration and the case of administering only PVP (molecular weight 60, 00). The results are shown in Fig. 2.
- composition for preventing and treating free radical disease of the present invention as described above.
- radical disease drugs that use conventional antioxidants as the main agent, which are easily oxidized and difficult to maintain quality after the formulation process or formulation, the activity is not lost in the formulation and in vivo. It is stable, safe and has almost no side effects, and has an excellent free radical scavenging activity.
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Abstract
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US11/792,520 US20080206222A1 (en) | 2004-12-07 | 2005-08-05 | Preventive/Therapeutic Composition For Free Radical Disease |
EP05770604A EP1834637A4 (en) | 2004-12-07 | 2005-08-05 | COMPOSITION FOR THE PREVENTION / TREATMENT OF DISEASES THROUGH FREE RADICALS |
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JP2004/354271 | 2004-12-07 | ||
JP2004354271A JP2006160664A (ja) | 2004-12-07 | 2004-12-07 | フリーラジカル疾患予防治療用組成物 |
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EP (1) | EP1834637A4 (ja) |
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- 2005-08-05 KR KR1020077012856A patent/KR20070112762A/ko not_active Application Discontinuation
- 2005-08-05 EP EP05770604A patent/EP1834637A4/en not_active Withdrawn
- 2005-08-05 WO PCT/JP2005/014798 patent/WO2006061925A1/ja active Application Filing
- 2005-08-05 US US11/792,520 patent/US20080206222A1/en not_active Abandoned
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008063157A3 (en) * | 2006-10-25 | 2009-03-19 | Us Gov Health & Human Serv | A nanoparticle-based anticoagulant |
WO2008109033A1 (en) * | 2007-03-02 | 2008-09-12 | Luna Innovations Incorporated | Steroid derivatives of fullerenes |
EP1992339A1 (en) * | 2007-05-18 | 2008-11-19 | Saeed Sarkar | Use of a magnesium isotope for treating hypoxia and a medicament comprising the same |
US7879996B2 (en) | 2007-05-18 | 2011-02-01 | Saeed Sarkar | Water soluble compounds |
US8834932B2 (en) | 2011-12-19 | 2014-09-16 | Industry Technology Research Institute | Anticoagulant-conjugated carbon nanocapsule, antithrombotic agent containing thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2006160664A (ja) | 2006-06-22 |
EP1834637A1 (en) | 2007-09-19 |
US20080206222A1 (en) | 2008-08-28 |
EP1834637A4 (en) | 2008-09-10 |
KR20070112762A (ko) | 2007-11-27 |
CN101098684A (zh) | 2008-01-02 |
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