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    • 2. 发明申请
    • IMPLEMENTATION OF STORING SECRET INFORMATION IN DATA STORAGE READER PRODUCTS
    • 数据存储阅读器产品中存储秘密信息的实现
    • WO03077084A2
    • 2003-09-18
    • PCT/US0304862
    • 2003-02-20
    • SANDISK CORPCHANG ROBERT CLI PINGSABET-SHARGHI FARSHID
    • CHANG ROBERT CLI PINGSABET-SHARGHI FARSHID
    • G06F21/00G06F1/00
    • G06F21/79G06F21/34G06F2221/2107
    • Methods and apparatus for enabling protected contents such as device keys to be stored on a reader are disclosed. According to one aspect of the present invention, a method for accessing a memory storage device that includes a memory and is coupled to a host system through an adapter, the memory storage device including a memory includes obtaining a key from the adapter. The key is suitable for encrypting information that is arranged to be stored in the memory, and is also suitable for decrypting the encrypted information. The method also includes processing the information using the key. In one embodiment, the information is stored in the memory, and the obtaining the information that is stored in the memory by processing the information such that the information may be decrypted using the key.
    • 公开了用于使受保护的内容(诸如设备密钥)能够存储在读取器上的方法和装置。 根据本发明的一个方面,一种用于访问包括存储器并且通过适配器耦合到主机系统的存储器存储设备的方法,所述存储器存储设备包括存储器包括从所述适配器获取密钥。 密钥适用于加密存储在存储器中的信息,也适用于对加密信息进行解密。 该方法还包括使用密钥处理信息。 在一个实施例中,信息被存储在存储器中,并且通过处理信息来获得存储在存储器中的信息,使得可以使用密钥对信息进行解密。
    • 8. 发明申请
    • PHARMACEUTICAL COMPOSITIONS
    • 药物组合物
    • WO2012075253A2
    • 2012-06-07
    • PCT/US2011062837
    • 2011-12-01
    • NOVARTIS AGCAO YUHACKL WOLFGANGLI PINGLI SHOUFENGMIRZA TAHSEENZEHENDER HARTMUTZHU JIAHAO
    • CAO YUHACKL WOLFGANGLI PINGLI SHOUFENGMIRZA TAHSEENZEHENDER HARTMUTZHU JIAHAO
    • A61K9/16A61P35/00
    • C07D471/04A61K9/1617A61K9/1623A61K9/1635A61K9/1641A61K9/1694A61K31/00
    • The present invention relates to a pharmaceutical composition for the oral administration of a therapeutic compound of formula (I), which comprises granules that comprise at least therapeutic compound of formula (I) (see below), particularly 2-Methyl-2-[4-(3-methyl-2-oxo-8- quinolin-3-yl-2,3-dihydro-imidazo[4,5-c]quinolin-1-yl)-phenyl]-propionitrile or 8-(6-methoxy-pyridin-3-yl)-3-methyl-1-(4-piperazin-1-yl-3-trifluoromethyl-phenyl)-1,3-dihydro-imidazo[4,5-c]quinolin-2-one, or a tautomer thereof, or a pharmaceutically acceptable salt, or a hydrate or solvate thereof; at least one non-ionic surfactant that is Vitamin E-TPGS in an amount ranging from about 15 to about 80% by weight of the composition; and at least one a dissolution enhancing agent selected from polyethylene glycol, polyethylene oxide, and any combination of the foregoing. The present invention also relates to processes for making such pharmaceutical compositions; a kit comprising such pharmaceutical composition and the instructions provide that the pharmaceutical composition may be taken immediately to about thirty minutes after the consumption of food; and related uses and methods of treatment.
    • 本发明涉及用于口服施用式(I)的治疗性化合物的药物组合物,其包含至少包含式(I)的治疗性化合物(参见下文),尤其是2-甲基-2- [4 - (3-甲基-2-氧代-8-喹啉-3-基-2,3-二氢 - 咪唑并[4,5-c]喹啉-1-基) - 苯基] - 丙腈或8-(6-甲氧基 - 吡啶-3-基)-3-甲基-1-(4-哌嗪-1-基-3-三氟甲基 - 苯基)-1,3-二氢 - 咪唑并[4,5-c]喹啉-2-酮, 或其互变异构体,或其药学上可接受的盐或水合物或溶剂化物; 至少一种非离子表面活性剂,其量为组合物重量的约15至约80%的量的维生素E-TPGS; 和至少一种选自聚乙二醇,聚环氧乙烷和前述的任意组合的溶解增强剂。 本发明还涉及制造这种药物组合物的方法; 包含此类药物组合物和说明书的试剂盒提供了可以立即在食物消耗后约三十分钟服用药物组合物; 以及相关的用途和治疗方法。