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Pharmaceutical composition of sustained-release solid dispersion of pelubiprofen and method for producing the same

机译:贝洛洛芬缓释固体分散体的药物组合物及其制备方法

摘要

The present invention relates to a sustained-release solid dispersion preparation of pelubiprofen and, more specifically, to a sustained-release solid dispersion preparation of pelubiprofen comprising Eudragit® RL PO, Eudragit® RS PO, and aminoclay. Eudragit® RL PO and Eudragit® RS PO in the present invention are pH-independent polymer mixtures, which are insoluble but may swell at physiological pH, and thus when exposed in an aqueous medium, regulates penetration of a medium inside a matrix. In addition, aminoclay is a microenvironment pH regulator having a cationic layered nanosheet structure, which is effective in regulating a drug release rate in a solid matrix structure. Accordingly, the sustained-release solid dispersion preparation of pelubiprofen according to the present invention shows continuous drug release effects in the gastrointestinal tract and reduces the frequency of administration, and thus can be beneficially used in the future.
机译:本发明涉及贝洛洛芬的缓释固体分散体制剂,更具体地说,涉及包含RL PO,Eudragit®RS PO和氨基粘土的贝洛洛芬的缓释固体分散体制剂。本发明中的RL PO和Eudragit RS PO是不依赖于pH的聚合物混合物,它们不溶但可在生理pH下溶胀,因此当暴露于水性介质中时,可调节介质在基质内部的渗透。另外,氨基粘土是具有阳离子层状纳米片结构的微环境pH调节剂,可有效调节固体基质结构中的药物释放速率。因此,根据本发明的贝洛洛芬的缓释固体分散体制剂在胃肠道中显示出连续的药物释放作用,并减少了给药频率,因此可以在将来有益地使用。

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