首页> 外国专利> Composition for treating allergic and/or vasomotor rhinitis or allergic conjunctivitis by topical or oral administration, contains synergistic combination of non-sedating antihistamine and leukotriene antagonist

Composition for treating allergic and/or vasomotor rhinitis or allergic conjunctivitis by topical or oral administration, contains synergistic combination of non-sedating antihistamine and leukotriene antagonist

机译:通过局部或口服治疗变应性和/或血管舒缩性鼻炎或变应性结膜炎的组合物,包含非镇静抗组胺药和白三烯拮抗剂的协同组合

摘要

Pharmaceutical composition comprises (separately or in combination): (A) a non-sedating antihistamine (or its salt), other than compounds of the loratadine type; (B) a leukotriene antagonist (or its salt) comprising (B1) leukotriene D 4 antagonists, (B2) 5-lipoxygenase inhibitors or (B3) FLAP (5-lipoxygenase activating protein) antagonists; and (C) conventional carriers and/or extenders or auxiliaries. Independent claims are included for the following: (i) the use of a combination of (A)-(C) for the preparation of a medicament for use as above; (ii) a medicament comprising (A)-(C), for use as above; and (iii) the preparation of the medicaments, by mixing and formulating the appropriate components. - ACTIVITY : Antiallergic; antiinflammatory; ophthalmological. In tests for inhibition of ovalbumin-induced nasal mucosal permeability in sensitized rats, the degree of inhibition was 11% using azelastine alone at 0.01 mg/kg i.p., 7% using montelukast alone at 0.1 mg/kg i.p. and 40% using a combination of azelastine at 0.01 mg/kg i.p. and montelukast at 0.1 mg/kg i.p. - MECHANISM OF ACTION : Antihistamine; leukotriene D 4 antagonist; 5-lipoxygenase inhibitor; FLAP (5-lipoxygenase activating protein) antagonist.
机译:药物组合物包含(单独或组合):(A)除氯雷他定类型的化合物以外的非镇静性抗组胺药(或其盐); (B)白三烯拮抗剂(或其盐),其包含(B1)白三烯D 4拮抗剂,(B2)5-脂氧合酶抑制剂或(B3)FLAP(5-脂氧合酶活化蛋白)拮抗剂; (C)常规载体和/或增量剂或助剂。下列各项包括独立权利要求:(i)(A)-(C)的组合在制备用于上述用途的药物中的用途; (ii)用于上述用途的包含(A)-(C)的药物; (iii)通过混合和配制适当的成分来制备药物。 -活动:抗过敏;消炎(药;眼科的在抑制卵白蛋白引起的敏化大鼠鼻粘膜通透性的试验中,单独使用氮卓斯汀(0.01 mg / kg i.p.)的抑制率为11%,单独使用孟鲁司特以0.1 mg / kg i.p的抑制率为7%。并以0.01 mg / kg i.p.的氮卓斯汀组合使用40%和孟鲁司特以0.1 mg / kg的腹腔注射-作用机理:抗组胺药;白三烯D 4拮抗剂; 5-脂氧合酶抑制剂; FLAP(5-脂氧合酶激活蛋白)拮抗剂。

著录项

  • 公开/公告号DE10007203A1

    专利类型

  • 公开/公告日2001-08-23

    原文格式PDF

  • 申请/专利权人 ASTA MEDICA AG;

    申请/专利号DE20001007203

  • 申请日2000-02-17

  • 分类号A61K31/55;A61K31/47;

  • 国家 DE

  • 入库时间 2022-08-22 01:09:59

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