Rapid-Melt Compositions and Methods of Making Same
    6.
    发明申请
    Rapid-Melt Compositions and Methods of Making Same 审中-公开
    快速熔体组合物及其制备方法

    公开(公告)号:US20100010101A1

    公开(公告)日:2010-01-14

    申请号:US12501652

    申请日:2009-07-13

    申请人: S. Rao Cherukuri

    发明人: S. Rao Cherukuri

    IPC分类号: A61K47/04 A61K47/12

    摘要: The present invention provides a novel rapid-melt pharmaceutical composition comprising a binder, a super emulsifier, a diluent/bulking material; and an active ingredient. The present invention also provides a rapid-melt bead composition comprising a binder having a melting point from about 20 to about 90° C., an emulsifier; a diluent/bulking material; and an active ingredient. Further, the present invention provides a chew tablet composition comprising a binder; an emulsifier having a melting point of greater than about 40° C.; a diluent/bulking material; and an active ingredient. Methods of making the disclosed compositions are also described.

    摘要翻译: 本发明提供一种新型的快速熔融药物组合物,其包含粘合剂,超级乳化剂,稀释剂/填充材料; 和活性成分。 本发明还提供一种包含熔点约20-90℃的粘合剂的快速熔融珠组合物,一种乳化剂; 稀释剂/膨胀材料; 和活性成分。 此外,本发明提供一种包含粘合剂的咀嚼片组合物; 具有大于约40℃的熔点的乳化剂; 稀释剂/膨胀材料; 和活性成分。 还描述了制备所公开的组合物的方法。

    Rapidly disintegrating solid oral dosage form of liquid dispersions
    7.
    发明申请
    Rapidly disintegrating solid oral dosage form of liquid dispersions 审中-公开
    快速分散固体口服剂型的液体分散体

    公开(公告)号:US20070243248A1

    公开(公告)日:2007-10-18

    申请号:US11787115

    申请日:2007-04-12

    申请人: S. Rao Cherukuri

    发明人: S. Rao Cherukuri

    IPC分类号: A61K9/20

    摘要: Solid dose rapidly disintegrating compositions for administering pharmaceutical and nutritional supplement agents and methods for the preparation thereof are disclosed and described. Preparation methods which maintain the particulate size of an active agent at the pre-processing size in the final composition are further disclosed. The ability to maintain such particulate size provides a number of advantages, including improved bioavailability and more accurate dosing.

    摘要翻译: 公开和描述了用于施用药物和营养补充剂的固体剂量快速崩解组合物及其制备方法。 进一步公开了将最终组合物中预处理尺寸的活性剂的颗粒尺寸保持的制备方法。 保持这种颗粒尺寸的能力提供了许多优点,包括改进的生物利用度和更精确的给药。