首页> 外国专利> SOLID PHARMACEUTICAL COMPOSITION (OPTIONS), METHOD FOR PRODUCING SOLID PHARMACEUTICAL COMPOSITION (OPTIONS), TABLET (OPTIONS) AND METHOD FOR PRODUCING AMPHOR PARTICLES

SOLID PHARMACEUTICAL COMPOSITION (OPTIONS), METHOD FOR PRODUCING SOLID PHARMACEUTICAL COMPOSITION (OPTIONS), TABLET (OPTIONS) AND METHOD FOR PRODUCING AMPHOR PARTICLES

机译:固体药物组合物(选项),制备固体药物组合物的方法,片剂(片剂)和制造安瓿颗粒的方法

摘要

1. A solid pharmaceutical composition for oral administration comprising about 0.01 ÷ 20 wt.% IN-105, about 10 ÷ 60 wt.% Saturated or unsaturated C4-C12 fatty acids, their esters or salts, and at least three pharmaceutically acceptable excipients selected from the group comprising at least 10 wt.% disintegrant, 10 wt.% diluent, 0.5 wt.% lubricant, optionally including binders, plasticizers, penetration enhancers, or solubilizers. ! 2. The composition according to claim 1, in which the fatty acid is capric acid and / or lauric acid or their salts. ! 3. The composition according to claim 1, in which the fatty acid is a sodium caprate. ! 4. The composition according to claim 1, in which the binder component is selected from the group comprising polyvinylpyrrolidone, carboxymethyl cellulose, methyl cellulose, starch, gelatin, sugars, natural or synthetic gums, or combinations thereof. ! 5. The composition according to claim 4, in which the binder component is polyvinylpyrrolidone. ! 6. The composition according to claim 1, in which the diluents are selected from the group comprising calcium salts, cellulose or cellulose derivatives, palatinose, organic acids, sugar and sugar alcohols, pectic acid salts and combinations thereof. ! 7. The composition according to claim 6, in which the diluent is mannitol. ! 8. The composition according to claim 1, in which the baking powder is selected from the group comprising cross-linked polyvinylpyrrolidone, carboxymethyl cellulose, methyl cellulose, cation exchange resins, alginic acid, guar gum, and combinations thereof. ! 9. The composition according to claim 1, in which the lubricant is selected from the group including
机译:1.一种用于口服的固体药物组合物,其包含约0.01÷20wt。%的IN-105,约10÷60wt。%的饱和或不饱和C4-C12脂肪酸,其酯或盐以及至少三种选择的药学上可接受的赋形剂选自包括至少10重量%的崩解剂,10重量%的稀释剂,0.5重量%的润滑剂的组,任选地包括粘合剂,增塑剂,渗透促进剂或增溶剂。 ! 2.根据权利要求1的组合物,其中所述脂肪酸是癸酸和/或月桂酸或其盐。 ! 3.根据权利要求1的组合物,其中所述脂肪酸是癸酸钠。 ! 4.根据权利要求1的组合物,其中所述粘合剂组分选自聚乙烯吡咯烷酮,羧甲基纤维素,甲基纤维素,淀粉,明胶,糖,天然或合成树胶或其组合。 ! 5.根据权利要求4的组合物,其中所述粘合剂组分是聚乙烯吡咯烷酮。 ! 6.根据权利要求1的组合物,其中所述稀释剂选自钙盐,纤维素或纤维素衍生物,帕拉金糖,有机酸,糖和糖醇,果胶酸盐及其组合。 ! 7.根据权利要求6的组合物,其中稀释剂是甘露醇。 ! 8.根据权利要求1的组合物,其中所述发酵粉选自交联的聚乙烯吡咯烷酮,羧甲基纤维素,甲基纤维素,阳离子交换树脂,藻酸,瓜尔豆胶及其组合。 ! 9.根据权利要求1的组合物,其中润滑剂选自包括以下的组:

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