PHARMACEUTICAL LATRUNCULIN FORMULATIONS
    1.
    发明申请
    PHARMACEUTICAL LATRUNCULIN FORMULATIONS 有权
    药物LATRUNCULIN配方

    公开(公告)号:US20070225343A1

    公开(公告)日:2007-09-27

    申请号:US11680893

    申请日:2007-03-01

    IPC分类号: A61K31/427

    摘要: The present invention relates to an aqueous pharmaceutical formulation comprising at least one latrunculin and the formulation does not contain a substantial amount of dimethyl sulfoxide. In one embodiment, the present invention is directed to an aqueous pharmaceutical formulation comprising at least one latrunculin in an amount of 0.001-2% w/v, a non-ionic surfactant in an amount of 0.01-2% w/v, and a tonicity agent to maintain a tonicity between 200-400 mOsm/kG, at a pH between 4 to 8, wherein the latrunculin, the surfactant, and the tonicity agent are compatible in the formulation, and the formulation does not contain a substantial amount of dimethyl sulfoxide. The formulation is stable for at least six month at refrigerated temperature. The present invention further provides a method of reducing intraocular pressure, a method of treating glaucoma, a method of inhibiting wound healing after trabeculectomy, and a method of inhibiting angiogenesis.

    摘要翻译: 本发明涉及含有至少一种梭菌素的水性药物制剂,并且所述制剂不含有大量的二甲基亚砜。 在一个实施方案中,本发明涉及包含0.001-2%w / v的量的至少一种latrunculin的水性药物制剂,0.01-2%w / v的量的非离子表面活性剂,和 张力剂以保持200-400mOsm / kG之间的张力,在4至8之间的pH下,其中所述莱特乐宁,表面活性剂和张力剂在制剂中相容,并且制剂中不含有大量的二甲基 亚砜。 该制剂在冷藏温度下稳定至少6个月。 本发明还提供降低眼内压的方法,治疗青光眼的方法,小梁切除术后抑制伤口愈合的方法以及抑制血管发生的方法。