首页> 外国专利> Pharmaceutical enteric coated tablet and preparation method

Pharmaceutical enteric coated tablet and preparation method

机译:药物肠溶片及其制备方法

摘要

A pharmaceutical component for shaping an oral coating, including a pearl shaped, granular or granular nucleus and an anesthetic coating of the nucleus, The core comprises an acid emulsion with a content of 70% to 100% by weight, a polymer with a content of 0% to 10% by weight, and a solution with a content of 0% to 10% by weight, It also has a numb coating, including a copolymer of metabolized acids and a plasticizer,The intestinal coating protects the core in a low pH environment of 3 or less, and can release the drug to a pH value of 4.5 or more. The drug composition also includes an anti adhesive with a weight between 0.1% and 4.0%, and is within the pH adjustment range of the substance. The intestinal acid coating can reduce the incompatibility between the drug and the internal nucleic acid, as well as the incompatibility between the anesthetic or delayed release,Therefore, the necessity of two or less protective coatings between the linear acid coating and the core is eliminated, and the adjustment of pH value helps the copolymers to decompose rapidly, thus promoting the release of the substance more quickly.In the gastrointestinal region, the pH is 4.5 or greater. 3. A process for preparing the pharmaceutical composition of the gastrointestinal coating, including (a) preparing a dry mixture, including a drug, an adhesive and a selfless agentAnd a part of the dry mixture is separated; (b) a wet mass (a) of the dry mixture is formed in El Paso;(c) Extrude the humidity substance so as to form a high-power pearl shell and turn it into ashes, and contaminate the humidity with the part of dry substance on the aisle;(d) These pearls are coated with linear and plasticized coating polymers in an aqueous environment; and (E) these coated pearls are mixed with an anti adhesive.
机译:用于形成口腔包衣的药物成分,包括珍珠状,颗粒状或颗粒状核和麻醉剂的核衣。核包含含量为70%至100%(重量)的酸乳液,含量为70%的聚合物。 0%至10%的重量,溶液含量为0%至10%的重量,它还具有麻木的涂层,包括代谢酸和增塑剂的共聚物,肠衣可在低pH下保护核心在3以下的环境中,并且可以将药物释放到4.5以上的pH值。该药物组合物还包含重量在0.1%至4.0%之间的抗粘剂,并且该抗粘剂在该物质的pH调节范围内。肠酸涂层可以减少药物与内部核酸之间的不相容性以及麻醉药或延迟释放之间的不相容性,因此消除了在线性酸涂层和核心之间使用两个或更少保护性涂层的必要,调节pH值有助于共聚物迅速分解,从而促进物质的更快释放。在胃肠道区域,pH为4.5或更高。 3.一种胃肠道包衣的药物组合物的制备方法,其包括:(a)制备包含药物,粘合剂和无私试剂的干燥混合物,并分离干燥混合物的一部分; (b)在埃尔帕索(El Paso)中形成湿混合物(a);(c)挤出湿气物质,以形成大功率的珍珠壳并将其变成灰烬,并用一部分湿气污染湿气。过道上的干燥物质;(d)这些珍珠在水性环境中涂有线性和增塑的涂层聚合物; (E)将这些涂覆的珍珠与抗粘剂混合。

著录项

  • 公开/公告号CO5070679A1

    专利类型

  • 公开/公告日2001-08-28

    原文格式PDF

  • 申请/专利权人 BRISTOL - MYERS SQUIBB COMPANY;

    申请/专利号CO19990031289

  • 发明设计人 ISMAT ULLAH;

    申请日1999-05-21

  • 分类号A61K9/22;

  • 国家 CO

  • 入库时间 2022-08-22 01:25:52

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号