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QUICKLY DISSOLVING TABLETS CONTAINING CAPEZITABAN

机译:快速溶解含有卡培他班的片剂

摘要

1. A pharmaceutical film-coated composition comprising capecitabine and at least one disintegrating agent comprising a composition comprising mannitol (90%), crospovidone (5%) and polyvinyl acetate (5%), where the composition breaks down in an evaluation device Disintegration according to the US Pharmacopoeia standard in water at 37 ° C for less than 2.5 minutes and is characterized by a hardness of approximately 8-23 Cobb hardness units (SCU) .2. The composition according to claim 1, comprising capecitabine in an amount of from about 10% to about 50% based on the total core weight of the composition. The composition of claim 2, wherein the capecitabine content is from about 50 mg to about 1500 mg. The composition of claim 3, wherein the capecitabine content is from about 100 mg to about 750 mg. The composition according to claim 3, in which the content of capecitabine is 125 mg, 175 mg, 250 mg, 350 mg or 500 mg. The pharmaceutical composition according to claim 1, which in addition to the composition containing mannitol (90%), crospovidone (5%) and polyvinyl acetate (5%), includes an additional disintegrating agent selected from the group comprising crospovidone with a particle diameter in the range of from less than 15 μm (90%) to less than 400 μm (90%), croscarmellose sodium, starch glycolate sodium, low substitution hydroxypropyl cellulose, or any combination of the above disintegrating agents. 7. The composition of claim 6, wherein the content of the disintegrant is from about 10% to about 50% based on the weight of the unit dosage form. The composition according to claim 6, in which the content of disintegrating agent
机译:1.包含卡培他滨和至少一种崩解剂的药物膜包衣的组合物,所述崩解剂包括包含甘露醇(90%),交聚维酮(5%)和聚乙酸乙烯酯(5%)的组合物,其中所述组合物在评估装置中分解符合美国药典标准,在37°C的水中少于2.5分钟,其特点是硬度约为8-23 Cobb硬度单位(SCU)。2。 2.根据权利要求1的组合物,其包含基于组合物的总芯重为约10%至约50%的卡培他滨。 3.权利要求2的组合物,其中卡培他滨的含量为约50mg至约1500mg。 4.根据权利要求3所述的组合物,其中所述卡培他滨含量为约100mg至约750mg。 4.根据权利要求3的组合物,其中卡培他滨的含量为125mg,175mg,250mg,350mg或500mg。 2.根据权利要求1所述的药物组合物,其特征在于,所述组合物除了包含甘露醇(90%),交聚维酮(5%)和聚乙酸乙烯酯(5%)的组合物以外,还包含选自粒径为10μm的交聚维酮的其他崩解剂。范围从小于15μm(90%)到小于400μm(90%),交联羧甲基纤维素钠,羟乙酸淀粉钠,低取代羟丙基纤维素或上述崩解剂的任何组合。 7.权利要求6的组合物,其中崩解剂的含量基于单位剂型的重量为约10%至约50%。 7.根据权利要求6的组合物,其中崩解剂的含量

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