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GASTRIC-RETENTIVE ORAL DRUG DOSAGE FORMS FOR CONTROLLED RELEASE OF HIGHLY SOLUBLE DRUGS

机译:胃溶性口服药物剂量控制释放的高溶解度药物

摘要

Drugs that are freely or highly soluble in water are formulated as unit dosage forms by incorporating them into polymeric matrices comprised of high molecular weight hydrophilic polymers that swell upon imbibition of water. The dosage form can be a single compressed tablets, or two or three compressed tablets retained in a single gelatin capsule. The oral formulation is designed for gastric retention and controlled delivery of an incorporated drug into the gastric cavity, and thus administered, the drug is released from the matrix into the gastric fluid by solution diffusion. The swollen polymeric matrix, having achieved sufficient size, remains in the gastric cavity for several hours if administered while the patient is in the fed mode, and remains intact long enough for substantially all of the drug to be released before substantial erosion of the matrix occurs. The swelling matrix lowers the accessibility of the gastric fluid to the drug and thereby limits the drug release rate. This process, together with diffusion retardation by selection of specific polymers, polymer molecular weights, and other variables, results in a sustained and controlled delivery rate of the drug to the gastric environment.
机译:通过将其掺入由高分子量亲水性聚合物组成的聚合物基体中,使之自由或高度溶于水,这些聚合物基体在吸收水后会溶胀,从而制成单位剂型。该剂型可以是单个压制片剂,或保留在单个明胶胶囊中的两个或三个压制片剂。口服制剂被设计用于胃滞留和将掺入的药物控制地递送到胃腔中,并且因此被施用,药物通过溶液扩散从基质释放到胃液中。已达到足够大小的溶胀的聚合物基质,如果在患者处于进食模式下给药,则在胃腔中保留了数小时,并且保持完整的时间足以在基质发生实质性腐蚀之前释放出几乎所有的药物。 。溶胀基质降低了胃液对药物的可及性,从而限制了药物的释放速率。该过程以及通过选择特定聚合物,聚合物分子量和其他变量的扩散阻滞,导致药物向胃环境的持续和受控的递送速率。

著录项

  • 公开/公告号KR100545480B1

    专利类型

  • 公开/公告日2006-01-24

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR19997011439

  • 发明设计人 쉘존더블유.;루이-헬름제니;

    申请日1999-12-04

  • 分类号A61K9/20;

  • 国家 KR

  • 入库时间 2022-08-21 21:24:24

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