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Non-irritating, non-sensitizing, non-ototoxic antibacterial ear preparations

机译:无刺激性,不致敏,无耳毒性的抗菌耳剂

摘要

The invention is directed to an aqueous non-ototoxic, topical, otic pharmaceutical composition of matter for treating a mammal consisting essentially of: ciprofloxacin or a pharmaceutically acceptable salt thereof in aqueous solution in an amount effective for antibacterial action; hydrocortisone or a pharmaceutically acceptable salt thereof in an amount effective as an anti-inflammatory agent; polyvinyl alcohol at least about 85% hydrolyzed in an amount effective to suspend the hydrocortisone in solution; water sufficient to produce an aqueous composition; benzyl alcohol in an amount effective for antibacterial action; lecithin in an amount effective for enhancing suspension of other constituents in the composition; and polysorbate ranging from polysorbate 20 to 80 in an amount effective for spreading the preparation on a hydrophobic skin surface to the site of infection or inflammation.
机译:本发明涉及一种用于治疗哺乳动物的无耳毒性的局部耳用水性药物组合物,该药物组合物主要由以下成分组成:环丙沙星或其药学上可接受的盐在水溶液中的含量为有效的抗菌作用;氢化可的松或其药学上可接受的盐,其有效量为抗炎剂;至少水解约85%的聚乙烯醇,其有效量可将氢化可的松悬浮在溶液中;足以产生水性组合物的水;有效量的苯甲醇具有抗菌作用;有效量的卵磷脂可增强组合物中其他成分的悬浮性;聚山梨酯的量为20至80,有效地使制剂在疏水性皮肤表面上散布到感染或炎症部位。

著录项

  • 公开/公告号DK0782448T3

    专利类型

  • 公开/公告日2002-07-08

    原文格式PDF

  • 申请/专利权人 BAYER AKTIENGESELLSCHAFT;

    申请/专利号DK19960917172T

  • 发明设计人 PURWAR SHIVAJI;GOLDMAN DAVID;

    申请日1996-06-05

  • 分类号A61K31/57;A01N43/40;A01N43/82;A61K31/56;A61P27/16;

  • 国家 DK

  • 入库时间 2022-08-22 00:45:37

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