Chinese herbal composition for treating eczema and psoriasis
    1.
    发明授权
    Chinese herbal composition for treating eczema and psoriasis 失效
    用于治疗湿疹和牛皮癣的中草药组合物

    公开(公告)号:US06676975B2

    公开(公告)日:2004-01-13

    申请号:US10074039

    申请日:2002-02-14

    IPC分类号: A61K3578

    摘要: This application relates to a material which is suitable for the treatment of atopic disease, non-atopic eczema or psoriasis. The material can be extracted from a freeze-dried decoction of a mixture comprising the following Chinese herbs: Radix Ledebouriella, Fructus Tribuli, Herba Potentilla chinensis, Caulis Clematis armandii, Radix Rehmannia, Radix Glycyrrhiza, Radix Paeonia rubra, Cortex Dictamni radicis, Herba Lopatheri, Spica Schizonepetae. The material comprises one or more of those components present in the freeze-dried decoction which run with Rf values in the ranges 0.00 to 0.100, 0.167 to 0.300, 0.400 to 0.533, 0.700 to 0.833 or 0.900 to 0.967 if the freeze-dried decoction is diluted in aqueous solution and subjected to chromatography on a Whatman 2 cms×55 cms×3 mm cellulose strip for 10 hours using a solvent mixture of butanol, ethanol and water in the proportions 4:1:1.

    摘要翻译: 本申请涉及适用于治疗特应性疾病,非特应性湿疹或牛皮癣的材料。 该材料可以从包含以下中草药的混合物的冷冻干燥汤中提取:枸杞,枸杞,中华Her草,铁线莲,地黄,甘草,芍药,茯苓,草本茯苓 ,Spica Schizonepetae。 该物质包含存在于冷冻干燥煎煮中的一种或多种组分,如果冷冻干燥的煎煮是在冰冷干燥汤中,则以Rf值为范围为0.00至0.100,0.167至0.300,0.400至0.533,0.700至0.833或0.900至0.967 在水溶液中稀释,并在Whatman 2 cmsx55 cmsx3 mm纤维素条上进行色谱分离,使用丁醇,乙醇和水的溶剂混合物,比例为4:1:1。

    Chinese herbs extract
    2.
    发明授权
    Chinese herbs extract 失效
    中药提取物

    公开(公告)号:US06399112B1

    公开(公告)日:2002-06-04

    申请号:US08750848

    申请日:1996-12-24

    IPC分类号: A61K3578

    摘要: This application relates to a material which is suitable for the treatment of atopic disease, non-atopic eczema or psoriasis. The material can be extracted from a freeze-dried decoction of a mixture comprising the following Chinese herbs: Radix Ledebouriella, Fructus Tribuli, Herba Potentilla chinensis, Caulis Clematis armandii, Radix Rehmannia, Radix Glycyrrhiza, Radix Paeonia rubra, Cortex Dictamni radicis, Herba Lopatheri, Spica Schizonepetae. The material comprises one or more of those components present in the freeze-dried decoction which run with Rf values in the ranges 0.00 to 0.100, 0.167 to 0.300, 0.400 to 0.533, 0.700 to 0.833 or 0.900 to 0.967 if the freeze-dried decoction is diluted in aqueous solution and subjected to chromatography on a Whatman 2 cms×55 cms×3 mm cellulose strip for 10 hours using a solvent mixture of butanol, ethanol and water in the proportions 4:1:1.

    摘要翻译: 本申请涉及适用于治疗特应性疾病,非特应性湿疹或牛皮癣的材料。 该材料可以从包含以下中草药的混合物的冷冻干燥汤中提取:枸杞,枸杞,中华Her草,铁线莲,地黄,甘草,芍药,茯苓,草本茯苓 ,Spica Schizonepetae。 该物质包含存在于冷冻干燥煎煮中的一种或多种组分,如果冷冻干燥的煎煮是在冰冷干燥汤中,则以Rf值为范围为0.00至0.100,0.167至0.300,0.400至0.533,0.700至0.833或0.900至0.967 在水溶液中稀释,并在Whatman 2 cmsx55 cmsx3 mm纤维素条上进行色谱分离,使用丁醇,乙醇和水的溶剂混合物,比例为4:1:1。

    Chinese herbs extract
    3.
    发明授权
    Chinese herbs extract 失效
    中药提取物

    公开(公告)号:US07341746B2

    公开(公告)日:2008-03-11

    申请号:US10716506

    申请日:2003-11-20

    IPC分类号: A61K36/00

    摘要: This application relates to a material which is suitable for the treatment of atopic disease, non-atopic eczema or psoriasis. The material can be extracted from a freeze-dried decoction of a mixture comprising the following Chinese herbs: Radix Ledebouriella, Fructus Tribuli, Herba Potentilla chinensis, Caulis Clematis armandii, Radix Rehmannia, Radix Glycyrrhiza, Radix Paeonia rubra, Cortex Dictamni radicis, Herba Lopatheri, Spica Schizonepetae. The material comprises one or more of those components present in the freeze-dried decoction which run with Rf values in the ranges 0.00 to 0.100, 0.167 to 0.300, 0.400 to 0.533, 0.700 to 0.833 or 0.900 to 0.967 if the freeze-dried decoction is diluted in aqueous solution and subjected to chromatography on a Whatman 2 cms×55 cms×3 mm cellulose strip for 10 hours using a solvent mixture of butanol, ethanol and water in the proportions 4:1:1.

    摘要翻译: 本申请涉及适用于治疗特应性疾病,非特应性湿疹或牛皮癣的材料。 该材料可以从包含以下中草药的混合物的冷冻干燥汤中提取:枸杞,枸杞,中华Her草,铁线莲,地黄,甘草,芍药,茯苓,草本茯苓 ,Spica Schizonepetae。 该物质包含存在于冷冻干燥煎煮中的一种或多种组分,如果冷冻干燥的煎煮是在冰冷干燥汤中,则以Rf值为范围为0.00至0.100,0.167至0.300,0.400至0.533,0.700至0.833或0.900至0.967 在水溶液中稀释,并在Whatman 2 cmsx55 cmsx3 mm纤维素条上进行色谱分离,使用丁醇,乙醇和水的溶剂混合物,比例为4:1:1。

    PHARMACEUTICAL FORMULATION
    4.
    发明申请

    公开(公告)号:US20130245109A9

    公开(公告)日:2013-09-19

    申请号:US13486227

    申请日:2012-06-01

    IPC分类号: A61K9/00

    摘要: The invention relates to pharmaceutical formulations, and more particularly to formulations containing cannabinoids for administration via a pump action spray. In particular, the invention relates to pharmaceutical formulations, for use in administration of lipophilic medicaments via mucosal surfaces, comprising: at least one lipophilic medicament, a solvent and a co-solvent, wherein the total amount of solvent and co-solvent present in the formulation is greater than 55% wt/wt of the formulation and the formulation is absent of a self emulsifying agent and/or a fluorinated propellant.

    Artemisia judaica fractionation method
    6.
    发明授权
    Artemisia judaica fractionation method 失效
    青蒿分选方法

    公开(公告)号:US06350478B1

    公开(公告)日:2002-02-26

    申请号:US08826419

    申请日:1997-03-27

    IPC分类号: A61K3578

    CPC分类号: A61K36/282 A61K2300/00

    摘要: Extracts of herbs of the Artemisia family, some of which have been known in traditional medicine to have anti-diabetic effects, are fractionated chromatographically to remove unacceptable mutagenetic properties while retaining effectiveness against Diabetes mellitus. Certain fractions are found to be insulinomemetic while others have glucagon antagonistic properties. Mixtures of such fractions have optimum clinical effect.

    摘要翻译: 艾滋病家族的草药提取物,其中一些在传统医学中已知具有抗糖尿病作用,经色谱分级分离,以消除不可接受的诱变特性,同时保留对糖尿病的有效性。 发现某些级分是胰岛素抑制剂,而另一些则具有胰高血糖素拮抗性质。 这些级分的混合物具有最佳的临床效果。

    Pharmaceutical formulation
    7.
    发明授权
    Pharmaceutical formulation 有权
    药物制剂

    公开(公告)号:US08211946B2

    公开(公告)日:2012-07-03

    申请号:US12704729

    申请日:2010-02-12

    IPC分类号: A01N65/00 A61K36/00

    摘要: The invention relates to pharmaceutical formulations, and more particularly to formulations containing cannabinoids for administration via a pump action spray. In particular, the invention relates to pharmaceutical formulations, for use in administration of lipophilic medicaments via mucosal surfaces, comprising: at least one lipophilic medicament, a solvent and a co-solvent, wherein the total amount of solvent and co-solvent present in the formulation is greater than 55% wt/wt of the formulation and the formulation is absent of a self emulsifying agent and/or a fluorinated propellant.

    摘要翻译: 本发明涉及药物制剂,更具体地涉及含有通过泵作用喷雾给药的大麻素的制剂。 特别地,本发明涉及用于通过粘膜表面施用亲脂性药物的药物制剂,其包含:至少一种亲脂性药物,溶剂和共溶剂,其中存在于溶剂和共溶剂中的溶剂和共溶剂的总量 制剂大于制剂的55重量%/重量,并且制剂不含自乳化剂和/或氟化推进剂。

    PHARMACEUTICAL FORMULATION
    9.
    发明申请
    PHARMACEUTICAL FORMULATION 有权
    药物制剂

    公开(公告)号:US20130109747A1

    公开(公告)日:2013-05-02

    申请号:US13486227

    申请日:2012-06-01

    IPC分类号: A61K9/00

    摘要: The invention relates to pharmaceutical formulations, and more particularly to formulations containing cannabinoids for administration via a pump action spray. In particular, the invention relates to pharmaceutical formulations, for use in administration of lipophilic medicaments via mucosal surfaces, comprising: at least one lipophilic medicament, a solvent and a co-solvent, wherein the total amount of solvent and co-solvent present in the formulation is greater than 55% wt/wt of the formulation and the formulation is absent of a self emulsifying agent and/or a fluorinated propellant.

    摘要翻译: 本发明涉及药物制剂,更具体地涉及含有通过泵作用喷雾给药的大麻素的制剂。 特别地,本发明涉及用于通过粘膜表面施用亲脂性药物的药物制剂,其包含:至少一种亲脂性药物,溶剂和共溶剂,其中存在于溶剂和共溶剂中的溶剂和共溶剂的总量 制剂大于制剂的55重量%/重量,并且制剂不含自乳化剂和/或氟化推进剂。