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Pharmaceutical composition containing budesonide and formoterol

机译:包含布地奈德和福莫特罗的药物组合物

摘要

The present invention relates to inhalation formulations of drugs in the form of dry powder for inhalation administration, suitable for the treatment of obstructive diseases of the airways, such as asthma and chronic obstructive pulmonary disease (COPD). In particular, the invention relates to a pharmaceutical composition for inhalation comprising a first powder comprising budesonide or a pharmaceutically acceptable salt thereof, in an amount greater than 5% by weight of said first powder, leucine in an amount from 5 to 70% by weight of said first powder, lactose in an amount from 20 to 90% by weight of said first powder; a second powder comprising formoterol or a pharmaceutically acceptable salt thereof, in an amount greater than 1% by weight of said second powder, leucine in an amount from 5 to 70% by weight of said second powder, lactose in an amount from 20 to 90% by weight of said second powder and a third powder comprising a mixture of a first lactose which has an X50 from 35 to 75 μm, with a second lactose which has an X50 from 1.5 to 10 μm, the content of said first and second lactose in said mixture being respectively from 85% to 96% and from 4% to 15%. Said composition has a fine particle fraction (FPF) greater than 60% and a delivered fraction (DF) greater than 80%.
机译:本发明涉及用于吸入给药的干粉形式的药物的吸入制剂,其适合于治疗气道阻塞性疾病,例如哮喘和慢性阻塞性肺疾病(COPD)。特别地,本发明涉及用于吸入的药物组合物,其包含第一粉末,所述第一粉末的布地奈德或其药学上可接受的盐的量大于所述第一粉末的5重量%,亮氨酸的含量为5-70重量%。在所述第一粉末中,乳糖的量为所述第一粉末的20-90重量%;第二粉末,其包含福莫特罗或其药学上可接受的盐,其量大于所述第二粉末的1%(重量),亮氨酸占所述第二粉末的5-70%(重量),乳糖为20-90所述第二粉末和第三粉末的重量百分比,所述第一和第二乳糖的含量包括:X50为35至75μm的第一乳糖与X50为1.5至10μm的第二乳糖的混合物。在所述混合物中的含量分别为85%至96%和4%至15%。所述组合物具有大于60%的细颗粒分数(FPF)和大于80%的传递分数(DF)。

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