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    • 1. 发明申请
    • ADHESIVE FREE TOPICAL PHARMACEUTICAL FORMULATIONS
    • 粘合剂免费的局部药物制剂
    • WO1995023596A1
    • 1995-09-08
    • PCT/EP1995000791
    • 1995-03-02
    • THE BOOTS COMPANY PLCAGGARWAL, MeenaHAGUE, John, NevilleKHAN, Karrar, AhmadSMITH, Alan
    • THE BOOTS COMPANY PLC
    • A61K09/70
    • A61K9/70
    • An adhesive-free topical pharmaceutical formulation comprising an absorbent material wherein the absorbent material is impregnated with a pharmaceutical composition comprising a solution of a non-steroidal anti-inflammatory drug in a C2-4 alcohol. Suitably the non-steroidal antiinflammatory drug comprises ibuprofen, S(+)-ibuprofen, flurbiprofen, S(+)-flurbiprofen, R(-)-flurbiprofen, ketoprofen, S(+)-ketoprofen, piroxicam, or naproxen, including pharmaceutically acceptable salts of each and comprises 0.1-25 % by wight of the pharmaceutical composition. The C2-4 alcohol comprises 20-95 % by weight of the pharmaceutical composition. The pharmaceutical composition further comprises 0.01-90 % by weight of a co-solvent selected from propylene glycol, benzyl alcohol, isopropyl palmitate, isopropyl myristate, or polyvinylpyrrolidone. The formulation is preferably in the form of a wipe or a wrap-around. The formulations are useful for the local treatment of pain and inflammation.
    • 一种不含粘合剂的局部药物制剂,其包含吸收材料,其中吸收材料用包含非甾体抗炎药在C2-4醇中的溶液的药物组合物浸渍。 合适地,非甾体抗炎药包括布洛芬,S(+) - 布洛芬,氟比洛芬,S(+) - 氟比洛芬,R( - ) - 氟比洛芬,酮洛芬,S(+) - 酮洛芬,吡罗昔康或萘普生,包括药学上可接受的 各自的盐并且包含0.1-25%的药物组合物。 C2-4醇包含20-95重量%的药物组合物。 该药物组合物还包含0.01-90重量%的选自丙二醇,苯甲醇,棕榈酸异丙酯,肉豆蔻酸异丙酯或聚乙烯吡咯烷酮的共溶剂。 制剂优选为擦拭物或包裹物的形式。 该制剂可用于局部治疗疼痛和炎症。
    • 5. 发明申请
    • LIQUID AND SOLID DOSAGE FORMULATIONS CONTAINING DATE FRUIT (PHOENIX DACTYLIFERA)
    • 含有水果的液体和固体剂量配方(PHOENIX DACTYLIFERA)
    • WO2007107787A3
    • 2008-05-15
    • PCT/GB2007050124
    • 2007-03-15
    • KHAN KARRAR AHMAD
    • KHAN KARRAR AHMAD
    • A61K9/20A23L9/20A61K31/19A61K47/46
    • A61K9/0095A23L19/09A23L33/105A23L33/15A23L33/16A23L33/40A61K9/0056A61K9/2068A61K31/19A61K47/46
    • Oral liquid and solid dosage formulations comprise a homogeneous dispersion of date material in a finely divided form. The formulation may be of nutritional and/or therapeutic value. Alternatively, the processed dates in the liquid and solid form may function purely as an excipient, in particular as an agent capable of improving the palatability of a pharmaceutically active substance with an unpleasant taste. The liquid formulation may be prepared by dispersing stoned, but otherwise whole date material in water, and subjecting the dispersion to homogenisation. The solid dose formulation preferably takes the form of granules, a tablet or a lozenge, and is preferably prepared by a process that involves the formation of a homogeneous dispersion of the date material in water, mixing of the date dispersion with some or all of the further ingredients of the formulation, and drying to remove excess water.
    • 口服液体和固体剂量制剂包含细分形式的日期材料的均匀分散体。 制剂可具有营养和/或治疗价值。 或者,液体和固体形式的加工日期可以纯粹作为赋形剂,特别是作为能够改善具有不愉快味道的药物活性物质的适口性的试剂。 液体制剂可以通过将石头,但其他全部日期材料分散在水中并使分散体均化来制备。 固体剂量制剂优选采用颗粒剂,片剂或锭剂的形式,并且优选通过涉及在水中形成日期物质的均匀分散体的方法制备,所述方法是将日期分散体与部分或全部 制剂的其他成分,并干燥除去多余的水分。
    • 6. 发明申请
    • LIQUID AND SOLID DOSAGE FORMULATIONS CONTAINING DATES (PHOENIX DACTYLIFERA)
    • 液体和固体剂量配方(PHOENIX DACTYLIFERA)
    • WO2007107787A2
    • 2007-09-27
    • PCT/GB2007/050124
    • 2007-03-15
    • KHAN, Karrar Ahmad
    • KHAN, Karrar Ahmad
    • A23L9/20
    • A61K9/0095A23L19/09A23L33/105A23L33/15A23L33/16A23L33/40A61K9/0056A61K9/2068A61K31/19A61K47/46
    • Oral liquid and solid dosage formulations comprise a homogeneous dispersion of date material in a finely divided form. The formulation may be of nutritional and/or therapeutic value. Alternatively, the processed dates in the liquid and solid form may function purely as an excipient, in particular as an agent capable of improving the palatability of a pharmaceutically active substance with an unpleasant taste. The liquid formulation may be prepared by dispersing stoned, but otherwise whole date material in water, and subjecting the dispersion to homogenisation. The solid dose formulation preferably takes the form of granules, a tablet or a lozenge, and is preferably prepared by a process that involves the formation of a homogeneous dispersion of the date material in water, mixing of the date dispersion with some or all of the further ingredients of the formulation, and drying to remove excess water.
    • 口服液体和固体剂量制剂包含细分形式的日期材料的均匀分散体。 制剂可具有营养和/或治疗价值。 或者,液体和固体形式的加工日期可以纯粹作为赋形剂,特别是作为能够改善具有不愉快味道的药物活性物质的适口性的试剂。 液体制剂可以通过将石头,但其他全部日期材料分散在水中并使分散体均化来制备。 固体剂量制剂优选采用颗粒剂,片剂或锭剂的形式,并且优选通过涉及在水中形成日期物质的均匀分散体的方法制备,所述方法是将日期分散体与部分或全部 制剂的其他成分,并干燥除去多余的水分。