发明名称 Formulation of diclofenac
摘要 The present invention relates to methods for producing particles of diclofenac using dry milling processes as well as compositions comprising diclofenac, medicaments produced using diclofenac in particulate form and/or compositions, and to methods of treatment of an animal, including man, using a therapeutically effective amount of diclofenac administered by way of said medicaments.
申请公布号 US9173854(B2) 申请公布日期 2015.11.03
申请号 US201514621863 申请日期 2015.02.13
申请人 iCeutica Pty Ltd. 发明人 Dodd Aaron;Meiser Felix;Norret Marck;Russell Adrian;Bosch H William
分类号 A61K9/14;A61K31/196;C07C229/42;B82Y40/00;A61K9/51 主分类号 A61K9/14
代理机构 Fish & Richardson P.C. 代理人 Fish & Richardson P.C.
主权项 1. A solid oral unit dose of a pharmaceutical composition containing 18 mg of diclofenac acid, wherein the diclofenac acid has a median particle size, on a volume average basis, of less than 5000 nm and greater than 25 nm, and wherein the unit dose, when tested in vitro by USP Apparatus I (Basket) method of U.S. Pharmacopoeia at 100 rpm at 37° C. in 900 ml of 0.05% sodium lauryl sulfate in citric acid solution buffered to pH 5.75, has a dissolution rate of diclofenac acid such that 94%, by weight, is released by 75 minutes.
地址 Philadelphia PA US