首页> 外国专利> PHARMACEUTICAL COMPOSITION COMPRISING A SOLID DISPERSION WITH A POLYMER MATRIX CONTAINING A CONTINUOUS POLYDEXTROSE PHASE AND A CONTINUOUS PHASE OF A POLYMER OTHER THAN POLYDEXTROSE

PHARMACEUTICAL COMPOSITION COMPRISING A SOLID DISPERSION WITH A POLYMER MATRIX CONTAINING A CONTINUOUS POLYDEXTROSE PHASE AND A CONTINUOUS PHASE OF A POLYMER OTHER THAN POLYDEXTROSE

机译:包含固体分散体和包含连续聚合物连续相以及聚合物以外的聚合物连续相的固体分散体的药物组合物

摘要

The invention relates to a solid pharmaceutical composition comprising a solid dispersion containing at least one active principle and a pharmaceutically-acceptable polymer matrix. The invention is characterised in that the pharmaceutically-acceptable polymer matrix comprises a mixture of (i) polydextrose, in the form of a continuous polydextrose phase, in order to favour the disintegration of the composition in an aqueous medium and (ii) at least one polymer other than polydextrose, in the form of a continuous phase, whereby the polydextrose is in a concentration of at least 20 wt.- % and the at least one polymer other than polydextrose is in a concentration of at least 20 wt.- % in relation to the total weight of the pharmaceutically-acceptable polymer matrix.
机译:本发明涉及固体药物组合物,其包含含有至少一种活性成分的固体分散体和药学上可接受的聚合物基质。本发明的特征在于,药学上可接受的聚合物基质包含(i)以连续聚葡萄糖相形式存在的聚葡萄糖的混合物,以有利于组合物在水性介质中的崩解和(ii)至少一种除聚葡萄糖以外的聚合物以连续相的形式存在,其中聚葡萄糖的浓度为至少20重量%,并且除聚葡萄糖以外的至少一种聚合物的浓度为至少20重量%。与药学上可接受的聚合物基质的总重量的关系。

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