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    • 1. 发明授权
    • Controlled-release device and preparation process
    • 控制释放装置及制备工艺
    • US5776481A
    • 1998-07-07
    • US588921
    • 1996-01-19
    • Christian KarstThierry GozlanGuy DerrieuLuc Castelli
    • Christian KarstThierry GozlanGuy DerrieuLuc Castelli
    • A01K13/00A01K27/00A01M29/00A01N25/34A61D7/00A61K9/00
    • A01K27/007
    • Device capable of being used in combination with a restraining or ornamental collar or with any other support for animals, intended to make possible the controlled and optically continuous and complete release of chemical substances, including medicaments, for more or less lengthy, continuous or noncontinuous, periods and process for producing the said device. The device comprises a polymeric matrix enclosing at least one active substance capable of being released towards an appropriate area of an animal. The device is composed of at least one tubular component of any cross-section, containing at least one layer of flexible polymeric matrix containing at least one active substance, the length of the said tubular component can be regulated to adjust the daily dose of the active substance to the weight of the animal and the ratio of the external surface area of said tubular component to the thickness of its' wall is as great as possible to obtain linear removal of the active substance.
    • 能够与限制性或装饰性领结合使用的装置,或与动物的任何其它支持物一起使用的装置,其旨在使得化学物质(包括药物)的受控和光学连续和完全释放可能或多或少地长时间连续或不连续, 期间和用于生产所述装置的过程。 该装置包括聚合物基体,其包围能够朝向动物的适当区域释放的至少一种活性物质。 该装置由任何横截面的至少一个管状部件组成,其包含至少一层包含至少一种活性物质的柔性聚合物基质,可调节所述管状组分的长度以调节活性物质的日剂量 物质相对于动物的重量,并且所述管状部件的外表面积与其壁的厚度的比率尽可能大以获得活性物质的线性去除。
    • 2. 发明授权
    • Composition and system for oral administration to animals
    • 用于口服给予动物的组合物和系统
    • US6010720A
    • 2000-01-04
    • US615285
    • 1996-05-22
    • Guy DerrieuBernard RaynierJean-Luc PougnasLuc Castelli
    • Guy DerrieuBernard RaynierJean-Luc PougnasLuc Castelli
    • A23K1/16A01N25/00A23K1/00A23K1/18A61K9/00A61K9/20A61K9/10A61K9/16A61K47/32
    • A01N25/004A23K40/20A23K40/30A23K50/40A23K50/80A61K9/0056
    • Composition and system for oral administration of chemicals or medicaments, and applications thereof (for example as medicament, dietetic product, food product, bait). Said composition comprises essentially (a) from 3% to 20% by weight of at least one water-insoluble polymer selected from the polyamides and ethylene copolymers such as ethylene/vinyl acetate; (b) from 35% to 60% by weight of lipidic substances, at least one of these lipidic substances being solid at room temperature, the melting point of the solid lipidic substance(s) being lower than that of the polymer(s); (c) from 5% to 45% of at least one paletable substance; (d) from 0% to 50% of another suitable complementary ingredient. Said composition can be obtained by (i) melting of the solid lipidic substances at a temperature lower than the melting point of the polymer(s), and (ii) mixing of the polymer(s) and the other constituents at the same temperature as for (i). A method of preparing said systems and composition is also disclosed.
    • PCT No.PCT / FR94 / 01120 Sec。 371日期:1996年5月22日 102(e)日期1996年5月22日PCT 1994年9月27日PCT公布。 公开号WO95 / 08931 日期1995年04月6日化学品或药物的口服化合物和制剂及其应用(例如药物,饮食品,食品,诱饵)。 所述组合物基本上包含(a)3重量%至20重量%的至少一种选自聚酰胺和乙烯共聚物如乙烯/乙酸乙烯酯的水不溶性聚合物; (b)35%至60%重量的脂质物质,这些脂质物质中的至少一种在室温下为固体,固体脂质物质的熔点低于聚合物的熔点; (c)至少一种可定制物质的5%至45%; (d)0%至50%的另一种合适的互补成分。 所述组合物可以通过(i)在低于聚合物熔点的温度下熔化固体脂质物质获得,和(ii)将聚合物和其它组分在与 为我)。 还公开了制备所述体系和组合物的方法。
    • 6. 发明申请
    • Compositions for Oral Administration to Animals, Processes for Obtaining the Same and the Uses Thereof
    • 口头管理动物的组成,获取动物的过程及其用途
    • US20140343004A1
    • 2014-11-20
    • US14344246
    • 2012-08-31
    • Guy DerrieuGiancarlo Mazzola
    • Guy DerrieuGiancarlo Mazzola
    • A61K31/7048A61K31/4985A23K1/17A61K31/506
    • The present invention concerns a solid, palatable composition and its preparation process which, relative to the total weight of the composition, comprises: 5 to 30%, preferably 8 to 20% by weight of at least one fat chosen from among a liquid oil, a fat, wax or mixture thereof, the liquid oil not to represent more than 8% by weight of the composition; 0.001 to 85% by weight of at least one active substance; and 20 to 95%, preferably 40 to 70% by weight of at least one palatable material, for use thereof as medicinal product, nutraceutical or food supplement, for oral administration to mammals, except man, in particular for domestic animals such as dogs, cats or horses. The said solid composition is obtained by mixing the components, vaporising the fats, calibrating the dry, fluid granular material and compressing the granular material in a stock cube press.
    • 本发明涉及一种固体,可口的组合物及其制备方法,其相对于组合物的总重量包含:5-30%,优选8-20%重量的至少一种选自液体油, 脂肪,蜡或其混合物,液体油不占组合物重量的8%以上; 0.001〜85重量%的至少一种活性物质; 和20至95%,优选40至70重量%的至少一种可口的材料,用于作为医药产品,营养保健品或食品补充剂,用于口服哺乳动物,除了人,特别是家畜如狗, 猫或马。 所述固体组合物通过混合组分,蒸发脂肪,校准干燥的流体颗粒材料并在原料立方体压榨机中压缩颗粒材料而获得。
    • 9. 发明授权
    • Water soluble powder form compositions and their applications thereof
    • 水溶性粉末状组合物及其应用
    • US5935603A
    • 1999-08-10
    • US945246
    • 1997-12-22
    • Guy DerrieuJean-Luc PougnasOlivier Broussaud
    • Guy DerrieuJean-Luc PougnasOlivier Broussaud
    • A61K47/02A61K9/14A61K31/43A61K31/47A61K31/545
    • A61K47/02Y10S514/951
    • Water soluble, powder form compositions suitable for completely and rapidly dissolving active ingredients which usually only dissolve in water in the presence of base salts, such as antibiotics of the betalactamide family, for example penicillins and their derivatives, cephalosporins and their derivatives, or other active ingredients such as sulphamides and quinolones, for oral absorption thereof and their applications. The water soluble powder form compositions contain, in combination and in powder form, at least one water soluble active ingredient, not in salt form, and with an exclusively alkaline pH, an excess of one or more strong base salts, and one or more buffers comprising one or more substances and capable of maintaining the pH of the medium at a level below the normal solubilization pH of said active ingredient. Aqueous solution compositions obtained from said powder form compositions are also described.
    • PCT No.PCT / FR96 / 00635 Sec。 371 1997年12月22日第 102(e)日期1997年12月22日PCT提交1996年4月25日PCT公布。 公开号WO96 / 33743 日期1996年10月31日适用于完全和快速溶解活性成分的水溶性粉末形式组合物,其通常仅在碱盐存在下溶解在水中,例如betalactamide家族的抗生素,例如青霉素及其衍生物,头孢菌素及其 衍生物或其它活性成分,例如磺酰胺和喹诺酮,用于口服吸收及其应用。 水溶性粉末形式的组合物组合含有粉末形式的至少一种水溶性活性成分,不是盐形式,并且具有纯碱性pH,过量的一种或多种强碱盐和一种或多种缓冲液 包含一种或多种物质并能够将培养基的pH保持在低于所述活性成分的正常溶解pH的水平。 还描述了由所述粉末形式组合物获得的水溶液组合物。