Transdermal drug delivery system for anti-inflammatory analgesic agent comprising diclofenac diethylammonium salt, and the manufacturing method thereof
    1.
    发明授权
    Transdermal drug delivery system for anti-inflammatory analgesic agent comprising diclofenac diethylammonium salt, and the manufacturing method thereof 有权
    包含双氯芬酸二乙基铵盐的消炎止痛剂的透皮给药系统及其制造方法

    公开(公告)号:US06723337B1

    公开(公告)日:2004-04-20

    申请号:US09509303

    申请日:2000-06-19

    IPC分类号: A61F1302

    摘要: The invention herein relates to a transdermal drug delivery systern for anti-Inflammatory analgesic. agent comprising diclofenac diethylammonium salt, wherein a backing film (1), a matrix layer (2) containing active ingredients, a release liner (3) which is removed before application onto the skin are laminated therein. Mome particularly, the invention herein relates to a transdermal drug delivery system for anti-inflammatory analgesic agent comprising diclofenac diethylammonum salt, wherein the transdermal penetration and adhesion of the patch to the body are enhanced by means of a matrix layer which comprises a diclofenac diethylammonum salt as active ingredient in addition to acrylic polymer as adhesive constituent, non-ionic surfacant as absorption enhancer, terpene and dissolution assistant, and the volatile and non-volatile constituents of the composition arc separately applied therein for significantly reducing the manufacturing time thereof.

    摘要翻译: 本发明涉及用于抗炎镇痛剂的透皮药物递送系统。 包含双氯芬酸二乙基铵盐的药剂,其中背衬膜(1),含有活性成分的基质层(2),在施用于皮肤之前被去除的剥离衬垫(3)。 特别地,本发明涉及用于消炎止痛剂的透皮药物递送系统,其包括双氯芬酸二乙基铵盐,其中通过包含双氯芬酸二乙基铵盐的基质层增强贴片对身体的透皮渗透和粘附 作为除了作为粘合剂成分的丙烯酸类聚合物之外的活性成分,作为吸收促进剂的非离子表面活性剂,萜烯和溶解助剂以及组合物的挥发性和非挥发性组分分别施加在其中,以显着减少其制造时间。

    Indol carboxylic acid bispyridyl carboxamide derivatives, pharmaceutically acceptable salt thereof, preparation method and composition containing the same as an active ingredient
    3.
    发明授权
    Indol carboxylic acid bispyridyl carboxamide derivatives, pharmaceutically acceptable salt thereof, preparation method and composition containing the same as an active ingredient 有权
    吲哚羧酸双吡啶甲酰胺衍生物,其药学上可接受的盐,含有其作为活性成分的制备方法和组合物

    公开(公告)号:US08324246B2

    公开(公告)日:2012-12-04

    申请号:US12393528

    申请日:2009-02-26

    摘要: Disclosed herein are a new indole carboxylic acid bispyridyl carboxamide derivative, a preparation method thereof, and a composition for prevention or treatment of obesity, urinary disorders, and CNS disorders, containing the same as an active ingredient. Because the indole carboxylic acid bispyridyl carboxamide derivatives according to the present invention have high affinity for 5-HT2c receptors, act selectively on the 5-HT2c receptors, the derivatives rarely have adverse effects caused by other receptors. Because the derivatives effectively inhibit serotonin activity, they may be useful for treatment or prevention of obesity; urinary disorders such as urinary incontinence, premature ejaculation, erectile dysfunction, and prostatic hyperplasia; CNS disorders such as depression, anxiety, concern, panic disorder, epilepsy, obsessive-compulsive disorder, migraine, sleep disorder, withdrawal from drug abuse, Alzheimer's disease, and schizophrenia, associated with 5-HT2c receptors.

    摘要翻译: 本文公开了一种新的吲哚羧酸双吡啶羧酰胺衍生物及其制备方法,以及用于预防或治疗肥胖,尿失调和CNS障碍的组合物,其含有活性成分。 因为根据本发明的吲哚羧酸双吡啶甲酰胺衍生物对5-HT 2C受体具有高亲和力,因此选择性地对5-HT 2C受体起作用,所以衍生物很少具有由其它受体引起的不良作用。 由于衍生物有效抑制5-羟色胺活性,因此可用于治疗或预防肥胖症; 尿失禁如尿失禁,早泄,勃起功能障碍和前列腺增生; 与5-HT2c受体相关的诸如抑郁症,焦虑症,忧虑症,惊恐障碍,癫痫症,强迫症,偏头痛,睡眠障碍,药物滥用戒断,阿尔茨海默病和精神分裂症等CNS疾病。

    NOVEL SUBSTITUTED-1, 1-DIOXO-BENZO[1,2,4]THIADIAZIN-3ONES, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME
    4.
    发明申请
    NOVEL SUBSTITUTED-1, 1-DIOXO-BENZO[1,2,4]THIADIAZIN-3ONES, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME 审中-公开
    新的取代的1,1-二氧代苯并[1,2,4]噻二嗪-3-酮,其制备方法和含有其的药物组合物

    公开(公告)号:US20100035866A1

    公开(公告)日:2010-02-11

    申请号:US12293965

    申请日:2006-03-28

    CPC分类号: C07D285/24

    摘要: The present invention relates to compounds of substituted-1,1-dioxo-benzo[1,2,4]thiadiazin-3-ones acting as a 5HT6 receptor antagonist, a preparation method thereof, and a pharmaceutical composition containing the same for treatment of the central nervous system disorders. The compounds of substituted-1,1-dioxo-benzo[1,2,4]thiadiazin-3-ones according to the present invention have excellent binding affinity for the 5HT6 receptor and excellent selectivity for the 5HT6 receptor over other receptors. Also, the compounds reverse a disruption of PPI by apomorphine and don't show rotatod deficit in mice. Therefore the compounds according to the present invention may be valuably used for treatment of a 5HT6 receptor relating disorders.

    摘要翻译: 本发明涉及作为5HT6受体拮抗剂的取代-1,1-二氧代 - 苯并[1,2,4]噻二嗪-3-酮的化合物,其制备方法和含有该化合物的药物组合物,其用于治疗 中枢神经系统疾病。 根据本发明的取代的-1,1-二氧代 - 苯并[1,2,4]噻二嗪-3-酮的化合物对5HT6受体具有优异的结合亲和力,对其它受体的5HT6受体的选择性优异。 此外,化合物反转了阿朴吗啡对PPI的破坏,并且在小鼠中不显示旋转异位缺陷。 因此,根据本发明的化合物可以有价值地用于治疗5HT6受体相关疾病。

    Method for optimally determining sensor positions for acoustic pyrometry
    5.
    发明授权
    Method for optimally determining sensor positions for acoustic pyrometry 失效
    用于最佳确定声学高温测量的传感器位置的方法

    公开(公告)号:US06564164B1

    公开(公告)日:2003-05-13

    申请号:US09691653

    申请日:2000-10-18

    IPC分类号: G06F1500

    CPC分类号: G01K11/22

    摘要: A method for optimally determining sensor positions for an acoustic pyrometry, capable of obtaining a minimum number of sensors satisfying a given error limit and determining positions of the obtained number of sensors for error minimization, in which a predetermined number of sensors are arbitrarily arranged on sides of a rectangular sectional area to be measured and a transfer matrix is calculated with respect to positions of all the sensors, with effective independence values obtained for respective paths of each of the sensors by performing singular value decomposition with respect to the calculated transfer matrix and a total effective independence value of each of the sensors is obtained by summing up the effective independence values obtained for the respective paths, followed by having a smallest one of the obtained total effective independence valves removed from among the sensors and the above steps are repeated until the number of the remaining sensors becomes equal to a target valve.

    摘要翻译: 一种用于最佳地确定用于声学高温计的传感器位置的方法,其能够获得满足给定误差极限的最小数量的传感器,并且确定所获得的用于误差最小化的传感器数量的位置,其中预定数量的传感器被任意布置在侧面 对于要测量的矩形截面积,并且相对于所有传感器的位置计算传递矩阵,通过对于所计算的传递矩阵执行奇异值分解,获得针对每个传感器的相应路径的有效独立性值,以及 每个传感器的总有效独立性值通过对各个路径获得的有效独立性值进行求和,然后将获得的从传感器中去除的总有效独立阀中的最小一个重复直到 剩余传感器的数量等于焦油 得到阀门。