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    • 34. 发明申请
    • PARASITICIDAL COMPOSITION
    • PARASITICIDAL组合物
    • WO2005007241A1
    • 2005-01-27
    • PCT/GB2004/003006
    • 2004-07-12
    • NORBROOK LABORATORIES LIMITEDBLAKELY, WilliamCROMIE, Lillian
    • BLAKELY, WilliamCROMIE, Lillian
    • A61P33/14
    • A61K45/06A01N37/40A61K31/045A61K31/609A01N43/90A01N31/02A01N25/10A01N2300/00A61K2300/00
    • An anti-parasiticidal composition presented as a topical "pour-on" product for treating animals infected by parasites which are known to be susceptible to salicylanilides, especially closantel, alone or together with at least one other anti­ parasitic compound of the avermectin or milbemycin type and offers enhanced bioavailability of the salicylanilide by provision of a delivery system comprising at least 20%(v/v) of one or more alcohols, and optionally including a polymeric moiety selected from the group consisting of polyvinylpyrrolidone (PVP), polyoxypropylene/polyoxyethylene block copolymers (poloxamer), and polyethylene glycols (PEG), thereby improving the bioavailability of e.g. closantel (as assessed with respect to blood plasma levels of closantel).
    • 一种抗寄生虫组合物,其表现为局部“浇注” 产品,用于治疗已知容易受到水杨酰苯胺类,特别是氯苯腈类,单独或与至少一种其他抗sh药一起感染的寄生虫感染的动物; 通过提供包含至少20%(v / v)的一种或多种醇并且任选地包括选自聚乙烯吡咯烷酮的聚合物部分的递送系统提供增强的水杨酰苯胺的生物利用度,并提供增强的阿维菌素或米尔倍霉素类型的寄生化合物 (PVP),聚氧丙烯/聚氧乙烯嵌段共聚物(泊洛沙姆)和聚乙二醇(PEG),由此提高例如 closantel(根据closantel的血浆水平评估)。