首页> 外国专利> Intravitreal Injection of Triamcinolone acetonide suspensions for Low Viscosity, highly flocculated

Intravitreal Injection of Triamcinolone acetonide suspensions for Low Viscosity, highly flocculated

机译:玻璃体内注射曲安奈德混悬液以降低粘度,高度絮凝

摘要

Claim 1: an aqueous suspension composition particularly suitable for injection into the eye, where the suspension composition contains no Preservative, has a pH of 6 to 7.5, a viscosity of 2 - 12 cps, and a greater degree of Flocculation and 5, in which the composition of suspen Zion consisting essentially of: (a) 3.5 - 45% (W / V) Triamcinolone acetonide has a volume mean diameter of 3 - 10 mm; (b) 0,45 and 0,55% (W / V) Sodium CarboxyMethyl Cellulose; (c) 0002 - 0,02% (W / V) Polysorbate 80; (d) one or more pharmaceutically acceptable salts chloride as agents to adjust the tone in an amount sufficient to cause suspension composition possesses osmolarity 250 - 350 mOsm); and a buffering agent; Water for injection; and (f) (g) optionally a pH adjusting Agent to adjust the pH Up to 7.5.Claim 1: suspension Composition of claim 1, wherein the suspension composition comprising Sodium Chloride, potassium chloride, Calcium chloride and magnesium chloride. Claim 1: suspension Composition of claim 1, wherein the Buffering Agent comprises SODIUM ACETATE and sodium Citrate.Claim 1: an aqueous suspension composition particularly suitable for injection into the eye, where the suspension composition contains no Preservative, has a pH of 6 - 8, a viscosity of 2 - 12 cps, and a greater degree of Flocculation and 5, in which the composition of suspension Nsion consists essentially of: (a) 0.5 to 8.0% (W / V) of a poorly soluble Drug,Where the drug has a volume average diameter of 3 - 10 mm; (b) 0,45 and 0,55% (W / V) Sodium CarboxyMethyl Cellulose; (c) 0002 - 0.02% (W / V) Polysorbate 80 or tyloxapol; (d) one or more pharmaceutically acceptable salts of chloride as agents in accordance with the Tone; Water for injection On; (f) an optional buffering Agent,G) and optionally a pH adjusting Agent to adjust the pH to 6 - 8.Claim 1: suspension Composition of claim 14.Where the poorly soluble Drugs selected from the group consisting of drugs for the treatment of macular edema; Drugs for the treatment of retinal Vein Occlusion; drug for the treatment of Geographic atrophy; Drugs for the treatment of Dry Macular Degeneration related With age; and Drugs for the treatment of Wet Macular Degeneration related to EDAD. claim 16: suspension Composition of claim 1, wherein the tandospirone is poorly soluble drugs.
机译:权利要求1:特别适合于注射入眼睛的水性悬浮液组合物,其中该悬浮液组合物不含防腐剂,pH为6至7.5,粘度为2-12cps,并且絮凝度较高,其中5。悬浮的锡安组合物基本上由以下组成:(a)3.5-45%(W / V)曲安奈德的体积平均直径为3-10 mm; (b)0.45和0.55%(W / V)羧甲基纤维素钠; (c)0002-0.02%(W ​​/ V)聚山梨酯80; (d)一种或多种药学上可接受的盐氯化物作为调节色调的试剂,足以使混悬液的摩尔渗透压浓度为250-350 mOsm。和缓冲剂;注射用水; (1)。权利要求1的悬浮液组合物,其中所述悬浮液组合物包含氯化钠,氯化钾,氯化钙和氯化镁。权利要求1:权利要求1的悬浮液组合物,其中缓冲剂包括乙酸钠和柠檬酸钠。1,一种特别适合注射入眼睛的水性悬浮液组合物,其中该悬浮液组合物不含防腐剂,其pH为6-8。 ,粘度为2-12 cps,絮凝度更高,为5,其中悬浮液Nsion的组成主要由以下成分组成:(a)0.5至8.0%(W / V)的难溶性药物,药物的体积平均直径为3-10毫米; (b)0.45和0.55%(W / V)羧甲基纤维素钠; (c)0002-0.02%(W ​​/ V)聚山梨酯80或泰洛沙泊; (d)一种或多种氯化物的药学上可接受的盐,作为根据该音调的试剂;注射用水(f)任选的缓冲剂,G)和任选的pH调节剂以将pH调节至6-8。权利要求1:悬浮液,根据权利要求14所述的组合物,其中所述难溶性药物选自用于治疗以下疾病的药物:黄斑水肿;用于治疗视网膜静脉阻塞的药物;用于治疗地理萎缩的药物;与年龄有关的干性黄斑变性的药物;和与EDAD相关的湿性黄斑变性的药物。 16.权利要求1的悬浮液组合物,其中所述tandospirone是难溶性药物。

著录项

  • 公开/公告号AR070824A1

    专利类型

  • 公开/公告日2010-05-05

    原文格式PDF

  • 申请/专利权人 ALCON RESEARCH LTD.;

    申请/专利号AR2009P100862

  • 发明设计人

    申请日2009-03-11

  • 分类号A61K31/573;A61K31/4523;A61K9/10;A61P27/02;

  • 国家 AR

  • 入库时间 2022-08-21 18:47:32

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