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Pharmaceutical dosage form for oral administration of hydrophilic drugs, particularly low molecular weight heparin

机译:亲水性药物特别是低分子量肝素的口服药物剂型

摘要

A delayed release pharmaceutical dosage form for oral administration of a hydrophilic drug, e.g., a polysaccharide drug such as low molecular weight heparin, are provided. The dosage form comprises a composition of: (a) a therapeutically effective amount of low molecular weight heparin; (b) a bile salt or bile acid; (c) at least one surfactant selected from hydrophilic surfactants, lipophilic surfactants, and mixtures thereof; and a means for delaying release of the composition from the dosage form following oral administration. Osmotic drug delivery systems for oral administration of a hydrophilic drug are also provided, wherein an osmotically activated device houses the drug, a bile salt or bile acid, and at least one surfactant selected from the group consisting of hydrophilic surfactants, lipophilic surfactants, and mixtures thereof. Methods for administering hydrophilic drugs, particularly polysaccharide drugs such as low molecular weight heparin, are also provided.
机译:提供了用于口服给药亲水性药物例如多糖药物如低分子量肝素的延迟释放药物剂型。该剂型包含以下组合物:(a)治疗有效量的低分子量肝素; (b)胆汁盐或胆汁酸; (c)至少一种选自亲水性表面活性剂,亲脂性表面活性剂及其混合物的表面活性剂;以及用于在口服给药后延迟从剂型释放组合物的手段。还提供了用于口服施用亲水性药物的渗透性药物递送系统,其中渗透激活的装置容纳药物,胆盐或胆汁酸,以及至少一种选自亲水性表面活性剂,亲脂性表面活性剂和混合物的表面活性剂。其。还提供了用于施用亲水性药物,特别是多糖药物如低分子量肝素的方法。

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