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    • 3. 发明专利
    • Eye drop for corneal epithelial defect treatment
    • 眼部上皮缺损治疗眼损伤
    • JP2012062269A
    • 2012-03-29
    • JP2010207110
    • 2010-09-15
    • Teika Seiyaku Kkテイカ製薬株式会社
    • SHIMATANI TAKAOKOBAYASHI MINORUARAKI TAKASHIARIKAWA CHIKAKO
    • A61K31/728A61K9/08A61K47/02A61K47/04A61K47/12A61K47/18A61P27/02
    • PROBLEM TO BE SOLVED: To provide a multi-dose type eye drop for corneal epithelial defect treatment containing hyaluronic acid at a high concentration of ≥0.3 w/v%, which has low cytotoxicity, is effectively prevented from decomposing thereby having high preservation efficacy and which has low irritation and satisfactory sense of use.SOLUTION: The multi-dose type eye drop for corneal epithelial defect treatment contains the following (a) to (c): (a) hyaluronic acid or its pharmacologically acceptable salt; (b) boric acid and/or borax; and (c) composed of the following (c1) and/or (c2): (c1) chlorhexidine or its pharmacologically acceptable salt; and (c2) p-hydroxy-benzoateester, wherein the blending quantity of the (a) hyaluronic acid or it pharmacologically acceptable salt is ≥0.3 w/v% to the whole of the formulation.
    • 要解决的问题:为了提供含有高浓度≥0.3w/ v%的透明质酸(其具有低细胞毒性)的角膜上皮缺损处理的多剂量眼滴,有效地防止了分解,从而具有高的 保鲜效果好,刺激性低,使用感好。 解决方案:角膜上皮缺损治疗的多剂量眼滴包含以下(a)至(c):(a)透明质酸或其药理学上可接受的盐; (b)硼酸和/或硼砂; 和(c)由以下(c1)和/或(c2)组成:(c1)氯己定或其药理学上可接受的盐; 和(c2)对羟基苯甲酸酯,其中(a)透明质酸或其药理学上可接受的盐的配合量相对于整个制剂为≥0.3w/ v%。 版权所有(C)2012,JPO&INPIT
    • 5. 发明专利
    • Ophthalmic agent
    • OPHTHALMIC代理
    • JP2009196988A
    • 2009-09-03
    • JP2009013505
    • 2009-01-23
    • Teika Seiyaku Kkテイカ製薬株式会社
    • SHIBUYA FUMINORISUGIYAMA KIYOSHIITO KIYOMIFUJISHITA SHIGETOKOBAYASHI MINORU
    • A61K31/365A61K31/245A61K47/02A61K47/10A61K47/12A61K47/18A61K47/32A61K47/34A61P27/02
    • PROBLEM TO BE SOLVED: To provide a stable and transparent ophthalmic agent containing fluorescein or its salt and oxybuprocaine or its salt and an ophthalmic agent which allows a long term storage at room temperature and under an unshaded environment.
      SOLUTION: The ophthalmic agent is for storage in plastic containers and contains one or not less than two kinds of preservatives selected from the group consisting of (A)-(E): (A) fluorescein or its salt, (B) oxybuprocaine or its salt, (C) a compound having buffer action, (D) a povidone and/or a nonionic surfactant, (E) sorbic acid and its salt, and paraben. Further the agent satisfies any one of the conditions (d1), (d2), and (d3): (d1) the amount of the povidone mixed is not less than 15 w/v% of the total amount of the ophthalmic agent, (d2) the amount of a povidone mixed is less than 15 w/v% of the total amount of the ophthalmic agent and including a nonionic surfactant, and (d3) free of a povidone and including a nonionic surfactant.
      COPYRIGHT: (C)2009,JPO&INPIT
    • 要解决的问题:提供一种含有荧光素或其盐的稳定且透明的眼用药剂和奥布对卡因或其盐和允许在室温和无阴影环境下长期储存的眼科剂。 (A) - (E):(A)荧光素或其盐,(B)和(B)中的一种或不少于两种防腐剂, (C)具有缓冲作用的化合物,(D)聚维酮和/或非离子表面活性剂,(E)山梨酸及其盐和对羟基苯甲酸酯。 此外,该试剂满足条件(d1),(d2)和(d3)中的任一条件:(d1)聚维酮的混合量不小于眼用试剂总量的15w / v%( d2)混合的聚维酮的量小于眼用试剂总量的15w / v%,并且包括非离子表面活性剂,和(d3)不含聚维酮并包括非离子表面活性剂。 版权所有(C)2009,JPO&INPIT