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    • 1. 发明申请
    • Processes for producing coenzyme Q10
    • 生产辅酶Q10的方法
    • US20110136191A1
    • 2011-06-09
    • US13020500
    • 2011-02-03
    • Kazuyoshi YAJIMATakahisa KATOAkihisa KANDAShiro KITAMURAYasuyoshi UEDA
    • Kazuyoshi YAJIMATakahisa KATOAkihisa KANDAShiro KITAMURAYasuyoshi UEDA
    • C12P7/22
    • C12P7/66C12P7/22
    • The present invention relates to a process for producing reduced coenzyme Q10 which comprises obtaining microbial cells containing reduced coenzyme Q10 at a ratio of not less than 70 mole % among the entire coenzymes Q10, optionally disrupting the cells and recovering thus produced reduced coenzyme Q10. The present invention also relates to a process for producing oxidized coenzyme Q10 which comprises either recovering oxidized coenzyme Q10 after oxidizing the above-mentioned microbial cells or disrupted product thereof, or recovering reduced coenzyme Q10 from the above-mentioned microbial cells or disrupted product thereof to oxidize thus-obtained reduced coenzyme Q10 thereafter. According to the processes of the present invention, reduced coenzyme Q10 and oxidized coenzyme Q10 can be produced simply on the industrial scale.
    • 本发明涉及一种还原型辅酶Q10的制备方法,其包括在整个辅酶Q10中获得含有还原型辅酶Q10比例不小于70摩尔%的微生物细胞,任选地破坏细胞并回收所生成的还原型辅酶Q10。 本发明还涉及氧化型辅酶Q10的制造方法,该方法包括在氧化上述微生物细胞或其破坏的产物后回收氧化型辅酶Q10,或将还原型辅酶Q10从上述微生物细胞或其破坏性产物回收至 此后氧化由此得到的还原型辅酶Q10。 根据本发明的方法,可以简单地在工业规模上制备还原型辅酶Q10和氧化型辅酶Q10。
    • 2. 发明授权
    • Processes for producing coenzyme Q10
    • 生产辅酶Q10的方法
    • US09315839B2
    • 2016-04-19
    • US13020500
    • 2011-02-03
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • C12P7/66C12P7/22
    • C12P7/66C12P7/22
    • The present invention relates to a process for producing reduced coenzyme Q10 which comprises obtaining microbial cells containing reduced coenzyme Q10 at a ratio of not less than 70 mole % among the entire coenzymes Q10, optionally disrupting the cells and recovering thus produced reduced coenzyme Q10. The present invention also relates to a process for producing oxidized coenzyme Q10 which comprises either recovering oxidized coenzyme Q10 after oxidizing the above-mentioned microbial cells or disrupted product thereof, or recovering reduced coenzyme Q10 from the above-mentioned microbial cells or disrupted product thereof to oxidize thus-obtained reduced coenzyme Q10 thereafter. According to the processes of the present invention, reduced coenzyme Q10 and oxidized coenzyme Q10 can be produced simply on the industrial scale.
    • 本发明涉及一种还原型辅酶Q10的制备方法,其包括在整个辅酶Q10中获得含有还原型辅酶Q10比例不小于70摩尔%的微生物细胞,任选地破坏细胞并回收所生成的还原型辅酶Q10。 本发明还涉及氧化型辅酶Q10的制造方法,该方法包括在氧化上述微生物细胞或其破坏的产物后回收氧化型辅酶Q10,或将还原型辅酶Q10从上述微生物细胞或其破坏性产物回收至 此后氧化由此得到的还原型辅酶Q10。 根据本发明的方法,可以简单地在工业规模上制备还原型辅酶Q10和氧化型辅酶Q10。
    • 3. 发明授权
    • Method for production of microcapsules using solid fat
    • 使用固体脂肪生产微胶囊的方法
    • US08496968B2
    • 2013-07-30
    • US12741565
    • 2008-11-06
    • Kento KanayaMasao SatoAkihisa Kanda
    • Kento KanayaMasao SatoAkihisa Kanda
    • A61K9/14A61K9/16
    • B01J13/04A23L33/10A23L33/175A23P10/35A61K9/5015A61K38/05A61K38/063
    • A method for production of fine microcapsules which encapsulate a hydrophilic bioactive substance at a high content and can be used in wide range of applications such as foods and medical drugs, which method enabling efficient industrial production, is provided. A method for production of S/O type microcapsules including the steps of: (1) emulsifying and dispersing a mixture of a solid fat and an aqueous solution containing a hydrophilic bioactive substance at a temperature of at least the melting point of the solid fat to obtain a W/O emulsion; (2) removing moisture in the W/O emulsion at a temperature of at least the melting point and lower than the boiling point of the solid fat to obtain an S/O suspension; (3) adding the S/O suspension into an aqueous phase containing at least one selected from a surfactant (B), a thickening agent and a hydrophilic organic solvent, and permitting liquid droplet dispersion at a temperature of at least the melting point and lower than the boiling point of the solid fat to obtain an S/O/W emulsion; and (4) cooling the S/O/W emulsion to lower than the melting point of the solid fat to harden the solid fat, and further removing the moisture at a temperature lower than the melting point of the solid fat.
    • 提供了以高含量包封亲水性生物活性物质的精细微胶囊的制造方法,可以广泛应用于食品,医药等领域,能够实现高效的工业化生产。 一种生产S / O型微胶囊的方法,包括以下步骤:(1)将固体脂肪和含有亲水性生物活性物质的水溶液的混合物在至少固体脂肪熔点的温度下乳化和分散至 获得W / O乳液; (2)在至少熔点低于固体脂肪沸点的温度下除去W / O乳液中的水分,得到S / O悬浮液; (3)将S / O悬浮液加入到含有选自表面活性剂(B),增稠剂和亲水性有机溶剂中的至少一种的水相中,并允许液滴在至少熔点和更低的温度下分散 比固体脂肪的沸点得到S / O / W乳液; 和(4)将S / O / W乳液冷却至低于固体脂肪的熔点,使固体脂肪硬化,并在低于固体脂肪熔点的温度下进一步除去水分。
    • 6. 发明申请
    • Processes for producing coenzyme Q10
    • 生产辅酶Q10的方法
    • US20080171373A1
    • 2008-07-17
    • US11981181
    • 2007-10-31
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • C12N9/00
    • C12P7/66C12P7/22
    • The present invention relates to a process for producing reduced coenzyme Q10 which comprises obtaining microbial cells containing reduced coenzyme Q10 at a ratio of not less than 70 mole % among the entire coenzymes Q10, optionally disrupting the cells and recovering thus-produced reduced coenzyme Q10. The present invention also relates to a process for producing oxidized coenzyme Q10 which comprises either recovering oxidized coenzyme Q10 after oxidizing the above-mentioned microbial cells or disrupted product thereof, or recovering reduced coenzyme Q10 from the above-mentioned microbial cells or disrupted product thereof to oxidize thus-obtained reduced coenzyme Q10 thereafter. According to the processes of the present invention, reduced coenzyme Q10 and oxidized coenzyme Q10 can be produced simply on the industrial scale.
    • 本发明涉及一种还原型辅酶Q 10的制备方法,该方法包括:将全部还原型辅酶Q 10的比例不小于70摩尔%的还原型辅酶Q 10 辅酶Q 10,任选地破坏细胞并回收如此生产的还原型辅酶Q 10。 本发明还涉及一种生产氧化型辅酶Q 10的方法,其包括在氧化上述微生物细胞或其破坏的产物之后回收氧化型辅酶Q 10,或 从上述微生物细胞中回收还原型辅酶Q 10 N或其破坏产物,从而氧化由此得到的还原型辅酶Q 10。 根据本发明的方法,可以简单地在工业规模上制备还原型辅酶Q 10和氧化型辅酶Q 10。
    • 8. 发明授权
    • Processes for producing coenzyme Q10
    • 生产辅酶Q10的方法
    • US07910340B2
    • 2011-03-22
    • US11981181
    • 2007-10-31
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • Kazuyoshi YajimaTakahisa KatoAkihisa KandaShiro KitamuraYasuyoshi Ueda
    • C12P1/00C12P7/66
    • C12P7/66C12P7/22
    • The present invention relates to a process for producing reduced coenzyme Q10 which comprises obtaining microbial cells containing reduced coenzyme Q10 at a ratio of not less than 70 mole % among the entire coenzymes Q10, optionally disrupting the cells and recovering thus-produced reduced coenzyme Q10. The present invention also relates to a process for producing oxidized coenzyme Q10 which comprises either recovering oxidized coenzyme Q10 after oxidizing the above-mentioned microbial cells or disrupted product thereof, or recovering reduced coenzyme Q10 from the above-mentioned microbial cells or disrupted product thereof to oxidize thus-obtained reduced coenzyme Q10 thereafter. According to the processes of the present invention, reduced coenzyme Q10 and oxidized coenzyme Q10 can be produced simply on the industrial scale.
    • 本发明涉及还原型辅酶Q10的制备方法,其包括在整个辅酶Q10中获得含有不少于70摩尔%的还原型辅酶Q10的微生物细胞,任选地破坏细胞并回收如此生产的还原型辅酶Q10。 本发明还涉及氧化型辅酶Q10的制造方法,该方法包括在氧化上述微生物细胞或其破坏的产物后回收氧化型辅酶Q10,或将还原型辅酶Q10从上述微生物细胞或其破坏性产物回收至 此后氧化由此得到的还原型辅酶Q10。 根据本发明的方法,可以简单地在工业规模上制备还原型辅酶Q10和氧化型辅酶Q10。
    • 9. 发明申请
    • METHOD FOR PRODUCTION OF MICROCAPSULES USING SOLID FAT
    • 使用固体脂肪生产微胶囊的方法
    • US20100297222A1
    • 2010-11-25
    • US12741565
    • 2008-11-06
    • Kento KanayaMasao ` SatoAkihisa Kanda
    • Kento KanayaMasao ` SatoAkihisa Kanda
    • A61K9/50A61K38/06A61K38/05A61P29/00A61P39/06A61P1/16
    • B01J13/04A23L33/10A23L33/175A23P10/35A61K9/5015A61K38/05A61K38/063
    • A method for production of fine microcapsules which encapsulate a hydrophilic bioactive substance at a high content and can be used in wide range of applications such as foods and medical drugs, which method enabling efficient industrial production, is provided. A method for production of S/O type microcapsules including the steps of: (1) emulsifying and dispersing a mixture of a solid fat and an aqueous solution containing a hydrophilic bioactive substance at a temperature of at least the melting point of the solid fat to obtain a W/O emulsion; (2) removing moisture in the W/O emulsion at a temperature of at least the melting point and lower than the boiling point of the solid fat to obtain an S/O suspension; (3) adding the S/O suspension into an aqueous phase containing at least one selected from a surfactant (B), a thickening agent and a hydrophilic organic solvent, and permitting liquid droplet dispersion at a temperature of at least the melting point and lower than the boiling point of the solid fat to obtain an S/O/W emulsion; and (4) cooling the S/O/W emulsion to lower than the melting point of the solid fat to harden the solid fat, and further removing the moisture at a temperature lower than the melting point of the solid fat.
    • 提供了以高含量包封亲水性生物活性物质的精细微胶囊的制造方法,可以广泛应用于食品,医药等领域,能够实现高效的工业化生产。 一种生产S / O型微胶囊的方法,包括以下步骤:(1)将固体脂肪和含有亲水性生物活性物质的水溶液的混合物在至少固体脂肪熔点的温度下乳化和分散至 获得W / O乳液; (2)在至少熔点低于固体脂肪沸点的温度下除去W / O乳液中的水分,得到S / O悬浮液; (3)将S / O悬浮液加入到含有选自表面活性剂(B),增稠剂和亲水性有机溶剂中的至少一种的水相中,并允许液滴在至少熔点和更低的温度下分散 比固体脂肪的沸点得到S / O / W乳液; 和(4)将S / O / W乳液冷却至低于固体脂肪的熔点,使固体脂肪硬化,并在低于固体脂肪熔点的温度下进一步除去水分。