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Microencapsulated or embedded medicaments prodn - by dispersing org. soln. of medicament and wall matl in carrier

机译:微囊化或包埋药物生产-通过分散组织。 soln。载体中的药物和壁基质

摘要

Encapsulated or embedded medicaments are produced by (a) dissolving a hydrophobic wall matl. (pref. a non-toxic synthetic high-mol. polymer) in =1 water-immiscible org. solvent having a b.pt. is not 100 degrees C, a vapour pressure greater than that of water and a dielectric constant is not 10, (b) dissolving or dispersing in the resulting soln. a medicament which is water-insol. or has a low solubility in water, (c) dispersing the resulting soln. or dispersion in a carrier (pref. an aq. hydrophilic colloid and/or an aq. anionic surfactant) so as to form fine droplets, and (d) evapg. the org. solvent. The process gives microcapsules under mild conditions so that the medicament is not decomposed. The microcapsules give excellent masking of unpleasant flavours and odours and improve the stability of the medicament. The microcapsules are so fine that they can be treated as dust-fine powders, and individual microcapsules contain practically identical amts. of medicament, making them partic. suitable for medicinal use.
机译:封装的或包埋的药物是通过(a)溶解疏水性壁材料制成的。 (首选无毒的合成高分子聚合物)> = 1与水不混溶的组织。 b.pt.的溶剂(b)溶解或分散在所得溶液中时,其温度不大于100摄氏度,蒸气压大于水且介电常数不大于10。水不溶性药物。或在水中的溶解度低,(c)将所得溶液分散。或分散在载体(优选亲水性胶体水溶液和/或阴离子表面活性剂水溶液)中以形成细小液滴,和(d)蒸发。组织。溶剂。该过程在温和的条件下产生了微胶囊,因此药物不会分解。微胶囊可很好地掩盖令人不快的味道和气味,并改善药物的稳定性。微胶囊是如此之细,以至于它们可以被视为粉尘细微的粉末,并且各个微胶囊实际上包含相同的酰胺。药物,使其变得颗粒状。适合药用。

著录项

  • 公开/公告号FR2245335B1

    专利类型

  • 公开/公告日1976-05-07

    原文格式PDF

  • 申请/专利权人 TOYO JOZO CY LTD;

    申请/专利号FR19730023653

  • 发明设计人

    申请日1973-06-28

  • 分类号A61J3/07;

  • 国家 FR

  • 入库时间 2022-08-23 01:52:51

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