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Complexes of the LHRH Antagonist Cetrorelix with Polyamino Acids and Methods for their Preparation

机译:LHRH拮抗剂Cetrorelix与聚氨基酸的配合物及其制备方法

摘要

In this invention, a release-delaying system is to be developed for LHRH antagonists, in particular for cetrorelix, which allows the active compound to be released in a controlled manner over several weeks by complexation with suitable biophilic carriers. The acidic polyamino acids polyglutamic acid and polyaspartic acid were selected for complexation with cetrorelix. The cetrorelix polyamino acid complexes are prepared from aqueous solutions by combination of the solutions and precipitation of the complexes, which are subsequently centrifuged off and dried over P2O5 in vacuo. If complexes having a defined composition are to be obtained, lyophilization proves to be a suitable method. The cetrorelix-carboxylic acid complexes were also prepared from the aqueous solutions. In the random liberation system, the acidic polyamino acids poly-Glu and poly-Asp showed good release-delaying properties as a function of the hydrophobicity and the molecular mass of the polyamino acid. In animal experiments, it was possible to confirm the activity of the cetrorelix-polyamino acid complexes as a depot system in principle. It is thus possible by complexation of cetrorelix with polyamino acids to achieve testosterone suppression in male rats over 600 hours. The release of active compound here can be controlled by the nature and the molecular mass of the polymers.
机译:在本发明中,将开发用于LHRH拮抗剂,特别是西曲瑞克的释放延迟系统,其允许活性化合物通过与合适的亲生物载体络合以受控方式在数周内释放。选择酸性聚氨基酸聚谷氨酸和聚天冬氨酸与西曲瑞克络合。 cetrorelix聚氨基酸复合物是由水溶液通过溶液的结合和复合物的沉淀制备的,随后将其离心分离并在P2O5中真空干燥。如果要获得具有确定组成的复合物,则冻干被证明是合适的方法。 cetrorelix-羧酸配合物也由水溶液制备。在随机释放系统中,酸性聚氨基酸聚-Glu和聚-Asp表现出良好的释放延迟特性,这是聚氨基酸的疏水性和分子量的函数。在动物实验中,原则上可以确认西曲瑞克-聚氨基酸复合物作为储库系统的活性。因此,通过将cetrorelix与聚氨基酸复合,可以在600小时内抑制雄性大鼠的睾丸激素。活性化合物的释放可以通过聚合物的性质和分子量来控制。

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