首页> 外国专利> MOSAPRIDE SUSTAINED-RELEASE FORMULATION PROVIDING PHARMACOLOGICAL AND CLINICAL EFFECTS WITH ONCE-DAILY ADMINISTRATION

MOSAPRIDE SUSTAINED-RELEASE FORMULATION PROVIDING PHARMACOLOGICAL AND CLINICAL EFFECTS WITH ONCE-DAILY ADMINISTRATION

机译:哌沙酮缓释制剂可通过一次有效的管理提供药理和临床作用

摘要

The formulation for oral administration of the present invention containing Mosapride or its salt is a double layer formulation consisting of a fast-release layer for rapid release of a drug and a sustained-release layer for slow release in order to simultaneously satisfy the rapid exhibition of pharmacological activities and sustained maintenance of pharmacological activities for 24-hours, wherein the high-viscosity hydroxypropyl methylcellulose (HPMC) and low-viscosity HMPC are used in mixture such that the content of a high viscosity HPMC as a controlled-release matrix within the sustained-release layer has a higher content, thereby capable of controlling the dissolution rate in the regions having different pH values within the gastrointestinal tract and/or the retention time in the gastrointestinal tract. Additionally, the formulation of the present invention is a small-sized preparation with a total weight of 200 mg or less, preferably 150 to 160 mg, thus capable of improving drug compliance of patients.
机译:含有莫沙必利或其盐的本发明的口服制剂是双层制剂,其由用于快速释放药物的速释层和用于缓慢释放的缓释层组成,以便同时满足快速释放药物的需要。药理活性和药理活性的持续维持24小时,其中将高粘度羟丙基甲基纤维素(HPMC)和低粘度HMPC混合使用,以使高粘度HPMC的含量作为持续释放的控释基质释放层的含量较高,因此能够控制在胃肠道内具有不同pH值的区域中的溶解速率和/或在胃肠道中的保留时间。另外,本发明的制剂是总重量为200mg或更少,优选150-160mg的小尺寸制剂,因此能够改善患者的药物依从性。

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