STABLE ORALLY DISINTEGRATING PHARMACEUTICAL COMPOSITIONS
    71.
    发明申请
    STABLE ORALLY DISINTEGRATING PHARMACEUTICAL COMPOSITIONS 审中-公开
    稳定的口腔崩解药物组合物

    公开(公告)号:WO2017216789A1

    公开(公告)日:2017-12-21

    申请号:PCT/IL2017/050652

    申请日:2017-06-13

    摘要: Described herein are stable orally disintegrating tablets containing a proton pump inhibitor, methods for making the same, and methods for treating subjects in need thereof. In particular, the orally disintegrating tablets are composed of a plurality of coated units admixed with a disintegrant that demonstrate decreased friability and increased hardness.

    摘要翻译: 本文描述了含有质子泵抑制剂的稳定的口腔崩解片剂,其制备方法以及治疗有需要的受试者的方法。 特别地,口腔崩解片剂由多个与崩解剂混合的涂布单元组成,所述单元显示出降低的脆性和增加的硬度。

    ANTIBIOTIC FORMULATION AND METHOD OF TREATMENT
    75.
    发明申请
    ANTIBIOTIC FORMULATION AND METHOD OF TREATMENT 审中-公开
    抗生素配方及治疗方法

    公开(公告)号:WO2007136664A3

    公开(公告)日:2008-05-02

    申请号:PCT/US2007011754

    申请日:2007-05-16

    发明人: RUBSAMEN REID

    摘要: A formulation comprised of particles which may be in groups and are comprised of a biocompatible polymer and an antimicrobial drug for controlled release of the drug is disclosed. The particles may be in an aqueous solution comprising thrombin and be dispersed in a gel. The formulation is administered to an area such as an open wound having an orthopedic implant therein and provides a therapeutically effective level of drug to the patient over therapeutically effective period of time.

    摘要翻译: 公开了一种由可以分组并由生物相容性聚合物组成的颗粒和用于药物控制释放的抗微生物药物组成的制剂。 颗粒可以在包含凝血酶的水溶液中并分散在凝胶中。 将制剂施用于其中具有矫形植入物的开放性伤口区域,并在治疗有效的时间段内向患者提供治疗有效水平的药物。

    カプセル皮膜用組成物、カプセル皮膜、及びこれを用いたカプセル剤
    79.
    发明申请
    カプセル皮膜用組成物、カプセル皮膜、及びこれを用いたカプセル剤 审中-公开
    胶囊,胶囊和胶囊的组合物

    公开(公告)号:WO2006011592A1

    公开(公告)日:2006-02-02

    申请号:PCT/JP2005/013916

    申请日:2005-07-29

    CPC分类号: A61K9/4825 A61K9/2873

    摘要:  本発明は、ゼラチン皮膜の経時的な溶解性低下をより高度に抑制し、特に軟カプセル剤の場合、同時にカプセルに十分な強度を付与するカプセル皮膜用組成物、並びにこれを用いたカプセル皮膜及びカプセル剤を提供する。該カプセル皮膜用組成物は、ゼラチン(A)と一般式C 6 H 12-n ・(H 2 PO 4 ) n (式中、nは1~6の整数を表す)で表されるイノシトールリン酸(B)とを含むことを特徴とする。

    摘要翻译: 用于胶囊膜形成的组合物,其有效地更高度地抑制明胶膜的溶解度随时间的降低,并且特别是当施用于软胶囊时,与胶囊同时赋予胶囊足够的强度; 以及由该组合物形成的胶囊膜和胶囊。 该组合物的特征在于包含由通式C 6 H 12-n H(H 2)表示的明胶(A)和磷酸肌醇(B) (其中n为1-6的整数)。

    TAMPER RESISTANT CO-EXTRUDED DOSAGE FORM CONTAINING AN ACTIVE AGENT AND AN ADVERSE AGENT AND PROCESS OF MAKING SAME
    80.
    发明申请
    TAMPER RESISTANT CO-EXTRUDED DOSAGE FORM CONTAINING AN ACTIVE AGENT AND AN ADVERSE AGENT AND PROCESS OF MAKING SAME 审中-公开
    含有活性剂和不良反应物的防篡改共挤出剂型及其制备方法

    公开(公告)号:WO2005055981A3

    公开(公告)日:2005-08-11

    申请号:PCT/US2004041154

    申请日:2004-12-08

    CPC分类号: A61K31/485 A61K9/5084

    摘要: The present invention relates to co-extruded pharmaceutical compositions and dosage forms including an active agent, such as an opioid agonist, and an adverse agent, such as an opioid antagonist. Such compositions and dosage forms are useful for preventing or discouraging tampering, abuse, misuse or diversion of a dosage form containing an active pharmaceutical agent, such as an opioid. The present invention also relates to methods of treating a patient with such a dosage form, as well as kits containing such a dosage form with instructions for using the dosage form to treat a patient.

    摘要翻译: 本发明涉及共挤出的药物组合物和剂型,其包含活性剂(诸如阿片样激动剂)和不利剂(诸如阿片样物质拮抗剂)。 此类组合物和剂型可用于预防或阻止含有活性药剂如阿片样物质的剂型的篡改,滥用,误用或转用。 本发明还涉及用这种剂型治疗患者的方法,以及含有这种剂型的试剂盒以及使用该剂型来治疗患者的说明书。