Sulfuric Acid Burn Treatment Composition
    92.
    发明申请
    Sulfuric Acid Burn Treatment Composition 审中-公开
    硫酸烧伤治疗组合物

    公开(公告)号:US20150147412A1

    公开(公告)日:2015-05-28

    申请号:US14547906

    申请日:2014-11-19

    申请人: Mark Greene

    发明人: Mark Greene

    摘要: Disclosed is a composition for treating sulfuric acid burn, wherein the composition may be used as a topical medication. The composition generally includes isopropyl alcohol or L-valine solution; at least one active therapeutic substance and/or a disinfectant for treating the burn; calcium hydroxide for neutralizing the acid; a humectant and/or a clinging agent for preventing the acid from spreading; an expectorant for signaling the body to clear any irritations caused by the acid; an acid indicator for visually signaling presence of the acid; and fumed silica as a thickening agent for slowing the reaction time of the acid. In a preferred embodiment, and without limitation, the therapeutic substances may include eugenol and thymol, and the disinfectants may include turmeric powder and hydrogen peroxide. Additionally, glycerin and sugar are used as clinging agents to reduce the chemical reaction between the sulfuric acid and surrounding tissue or materials exposed thereto.

    摘要翻译: 公开了用于治疗硫酸烧伤的组合物,其中该组合物可以用作局部用药。 组合物通常包括异丙醇或L-缬氨酸溶液; 至少一种用于治疗烧伤的活性治疗物质和/或消毒剂; 用于中和酸的氢氧化钙; 用于防止酸扩散的保湿剂和/或保持剂; 用于发出身体清除任何由酸引起的刺激的祛痰剂; 用于视觉上表示酸的存在的酸指示剂; 和热解法二氧化硅作为减缓酸的反应时间的增稠剂。 在优选的实施方案中,但不限于,治疗物质可以包括丁子香酚和百里酚,并且消毒剂可以包括姜黄粉和过氧化氢。 此外,甘油和糖用作粘附剂以减少硫酸和周围组织或暴露于其中的材料之间的化学反应。

    Viral inhibitor compositions for in vivo therapeutic use comprising a combination of (−)-carvone, geraniol and a further essential oil component
    93.
    发明授权
    Viral inhibitor compositions for in vivo therapeutic use comprising a combination of (−)-carvone, geraniol and a further essential oil component 有权
    用于体内治疗用途的病毒抑制剂组合物,其包含( - ) - 香芹酮,香叶醇和另外的精油成分

    公开(公告)号:US08980945B2

    公开(公告)日:2015-03-17

    申请号:US13582784

    申请日:2011-03-28

    申请人: Christine Coppens

    发明人: Christine Coppens

    摘要: The present invention concerns an antiviral composition comprising the following components: R-(−)-2-methyl-5-(prop-1-en-2-yl)-cyclohex-2-enone (also called (−) carvone) and S-(+)-2-methyl-5-(prop-1-en-2-yl)-cyclohex-2-enone (also called (+) carvone) and (2E)-3,7-dimethylocta-2,6-dien-1-ol (also called trans-geraniol) in combination with at least one more component chosen among essential oils components for use in treatment and prevention of diseases caused by DNA enveloped viruses, DNA non-enveloped viruses, RNA enveloped viruses and RNA non-enveloped viruses.

    摘要翻译: 本发明涉及包含以下组分的抗病毒组合物:R - ( - ) - 2-甲基-5-(丙-1-烯-2-基) - 环己-2-烯酮(也称为( - )香芹酮)和 S - (+) - 2-甲基-5-(丙-1-烯-2-基) - 环己-2-烯酮(也称为(+)香芹酮)和(2E)-3,7-二甲基辛-2 6-联烯-1-醇(也称为反式香叶醇)与至少一种选自用于治疗和预防由DNA包膜病毒引起的疾病,DNA非包膜病毒,RNA包膜病毒的精油成分中的组分组合 和RNA非包膜病毒。

    LEVOTHYROXINE FORMULATION WITH ACACIA
    96.
    发明申请
    LEVOTHYROXINE FORMULATION WITH ACACIA 有权
    乙酰胆碱配合ACACIA

    公开(公告)号:US20140178511A1

    公开(公告)日:2014-06-26

    申请号:US13723485

    申请日:2012-12-21

    申请人: Mylan Inc.

    摘要: A pharmaceutical composition comprising thyroxine, acacia, and an antioxidant selected from propyl gallate, butylated hydroxyanisol, and butylated hydroxytoluene is disclosed. The pharmaceutical composition has an improved shelf life. In one embodiment, the composition additionally comprises sucrose, microcrystalline cellulose, and mannitol. The pharmaceutical composition may be used for treating thyroid disorders by orally administering the composition to a patient in need thereof.

    摘要翻译: 公开了包含甲状腺素,阿拉伯胶和选自没食子酸丙酯,丁基化羟基苯甲醚和丁基化羟基甲苯的抗氧化剂的药物组合物。 药物组合物具有改善的保质期。 在一个实施方案中,组合物另外包含蔗糖,微晶纤维素和甘露糖醇。 该药物组合物可以通过将该组合物口服给予有需要的患者来治疗甲状腺疾病。

    METHOD FOR ENHANCING THE BIOAVALABILITY OF OSPEMIFENE
    100.
    发明申请
    METHOD FOR ENHANCING THE BIOAVALABILITY OF OSPEMIFENE 有权
    提高OSPEMIFENE生物稳定性的方法

    公开(公告)号:US20130324614A1

    公开(公告)日:2013-12-05

    申请号:US13904818

    申请日:2013-05-29

    申请人: Anttila Markku

    发明人: Anttila Markku

    IPC分类号: A61K31/085

    摘要: This invention relates to a method for enhancing the bioavailability of a therapeutically active compound of the formula (I) or a geometric isomer, a stereoisomer, a pharmaceutically acceptable salt, an ester thereof or a metabolite thereof, wherein said compound is administered orally to the individual in connection with the intake of food.

    摘要翻译: 本发明涉及增强式(I)的治疗活性化合物或几何异构体,立体异构体,药学上可接受的盐,其酯或代谢物的生物利用度的方法,其中所述化合物经口给予 个人与摄入食物有关。