首页> 外国专利> THREE-PHASE PHARMACEUTICAL FORM WITH CONSTANT AND CONTROLLED RELEASE OF AMORPHOUS ACTIVE COMPONENT FOR SINGLE DAILY ADMINISTRATION

THREE-PHASE PHARMACEUTICAL FORM WITH CONSTANT AND CONTROLLED RELEASE OF AMORPHOUS ACTIVE COMPONENT FOR SINGLE DAILY ADMINISTRATION

机译:单一给药每日均相和受控释放非晶态活性成分的三相药物形式

摘要

PCT No. PCT/SI96/00012 Sec. 371 Date Nov. 12, 1997 Sec. 102(e) Date Nov. 12, 1997 PCT Filed May 17, 1996 PCT Pub. No. WO96/36318 PCT Pub. Date Nov. 21, 1996Described is a novel three-phase pharmaceutical form with constant and controlled release of an amorphous active ingredient stabilized with polymers for a single daily peroral application, which is especially suitable for active ingredients existing in amorphous form or in one or more polymorphous forms, which exhibit poor solubility in crystal form depending on the polymorphous form, particle size and the specific surface area of the active ingredient. The active ingredient can be used in its amorphous or any polymorphous form, which in the process of the preparation of the three-phase pharmaceutical form according to the invention is converted into the amorphous form. The three-phase pharmaceutical form with constant and controlled release of an amorphous active ingredient for a single daily peroral application contains a core consisting of a first and a second phase and a coating representing the third phase. In the first phase the three-phase pharmaceutical form contains an amorphous active ingredient, the water-soluble polymer polyvinylpyrrolidone and a cellulose ether as carriers of the amorphous active ingredient and simultaneously as inhibitors of its crystallization, a surfactant that improves the solubility of the active ingredient and promotes the absorption of the amorphous active ingredient from gastrointestinal tract, in the second phase it contains a cellulose ether and a mixture of mono-, di- and triglycerides as sustained release agents and the third phase is represented by a poorly soluble or gastro-resistant film coating, which in the first few hours after the application controls the release of the active ingredient and can consist of an ester of hydroxypropylmethylcellulose with phthalic anhydride or of a copolymerizate based on methacrylic acid and ethyl acrylate. Described is also a process for the preparation of this pharmaceutical form.
机译:PCT号PCT / SI96 / 00012第371日期1997年11月12日102(e)日期:1997年11月12日; PCT申请日期:1996年5月17日。 PCT公开号WO96 / 36318。日期为1996年11月21日,描述了一种新型的三相药物形式,可稳定稳定地释放由聚合物稳定的无定形活性成分,可每日口服一次,特别适用于以无定形形式或以一种或多种形式存在的活性成分多晶型物,根据多晶型物,活性成分的粒径和比表面积,其在晶型中的溶解性差。活性成分可以以其无定形或任何多晶型形式使用,其在根据本发明的三相药物形式的制备过程中转化为无定形形式。用于单次每日口服施用的具有恒定和受控释放的无定形活性成分的三相药物形式包含由第一和第二相以及代表第三相的包衣组成的核心。在第一阶段中,三相药物形式包含无定形活性成分,水溶性聚合物聚乙烯吡咯烷酮和纤维素醚作为无定形活性成分的载体,同时作为其结晶的抑制剂,是一种改善活性成分溶解度的表面活性剂成分并促进无定形活性成分从胃肠道的吸收,在第二阶段它包含纤维素醚以及甘油单酯,甘油二酯和甘油三酸酯的混合物作为缓释剂,第三阶段以难溶性或胃肠道为代表-抗性膜包衣,其在施用后的最初几个小时内控制活性成分的释放,并且可以由羟丙基甲基纤维素与邻苯二甲酸酐的酯或基于甲基丙烯酸和丙烯酸乙酯的共聚酯组成。还描述了该药物形式的制备方法。

著录项

  • 公开/公告号CZ365597A3

    专利类型

  • 公开/公告日1998-04-15

    原文格式PDF

  • 申请/专利权人 LEK;

    申请/专利号CZ19970003655

  • 申请日1996-05-17

  • 分类号A61K9/22;

  • 国家 CZ

  • 入库时间 2022-08-22 02:58:22

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