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    • 4. 发明授权
    • Platinum (IV) complexes for use in dual mode pharmaceutical therapy
    • 用于双重模式药物治疗的铂(IV)复合物
    • US09265747B2
    • 2016-02-23
    • US13060354
    • 2009-08-26
    • Stephen J. LippardShanta Dhar
    • Stephen J. LippardShanta Dhar
    • A61K31/282A61K31/19A61K33/24A61K45/06
    • A61K31/282A61K31/19A61K33/24A61K45/06A61K2300/00
    • The present invention provides compositions, preparations, formulations, kits, and methods useful for treating subjects in need of therapeutic protocol, including subjects having cancer or at risk of developing cancer. Some embodiments of the invention may comprise a composition comprising a first component comprising a precursor to a therapeutically active platinum agent and a precursor to a second therapeutically active agent. The therapeutically active platinum agent and the second therapeutically active agent may dissociate from each other, thereby forming a first therapeutically active platinum agent and a second therapeutically active agent. The second therapeutically active gent may affect a cellular pathway of a cancer cell and may be substantially inactive towards non-cancerous cells.
    • 本发明提供了可用于治疗需要治疗方案的受治疗者的组合物,制剂,制剂,试剂盒和方法,包括具有癌症或有发展癌症风险的受试者。 本发明的一些实施方案可以包含包含第一组分的组合物,所述第一组分包含治疗活性铂剂的前体和第二治疗活性剂的前体。 治疗活性的铂剂和第二治疗活性剂可以彼此解离,从而形成第一治疗活性的铂剂和第二治疗活性剂。 第二治疗活性配偶可能影响癌细胞的细胞途径,并且可能对非癌细胞基本上无活性。
    • 6. 发明申请
    • PLATINUM (IV) COMPLEXES FOR USE IN DUAL MODE PHARMACEUTICAL THERAPY
    • 用于双模式药物治疗的白蛋白(IV)复合物
    • US20110257261A1
    • 2011-10-20
    • US13060354
    • 2009-08-26
    • Stephen J. LippardShanta Dhar
    • Stephen J. LippardShanta Dhar
    • A61K31/282A61P35/00C07F15/00
    • A61K31/282A61K31/19A61K33/24A61K45/06A61K2300/00
    • The present invention provides compositions, preparations, formulations, kits, and methods useful for treating subjects in need of therapeutic protocol, including subjects having cancer or at risk of developing cancer. Some embodiments of the invention may comprise a composition comprising a first component comprising a precursor to a therapeutically active platinum agent and a precursor to a second therapeutically active agent. The therapeutically active platinum agent and the second therapeutically active agent may dissociate from each other, thereby forming a first therapeutically active platinum agent and a second therapeutically active agent. The second therapeutically active gent may affect a cellular pathway of a cancer cell and may be substantially inactive towards non-cancerous cells.
    • 本发明提供了可用于治疗需要治疗方案的受治疗者的组合物,制剂,制剂,试剂盒和方法,包括具有癌症或有发展癌症风险的受试者。 本发明的一些实施方案可以包含包含第一组分的组合物,所述第一组分包含治疗活性铂剂的前体和第二治疗活性剂的前体。 治疗活性的铂剂和第二治疗活性剂可以彼此解离,从而形成第一治疗活性的铂剂和第二治疗活性剂。 第二治疗活性配偶可能影响癌细胞的细胞途径,并且可能对非癌细胞基本上无活性。
    • 8. 发明授权
    • Immune-stimulating photoactive hybrid nanoparticles
    • 免疫刺激光敏杂交纳米颗粒
    • US09517277B2
    • 2016-12-13
    • US14128238
    • 2012-07-11
    • Shanta DharJoshua ChoiSean Marrache
    • Shanta DharJoshua ChoiSean Marrache
    • A61K51/00A61M36/14A61K47/48A61K41/00
    • A61K47/48915A61K41/0071
    • Provides is a therapeutic technology that combines the phototoxic and immune-stimulating ability of photodynamic therapy with the widespread effectiveness of the immune system to reduce the viability of such as cancer cells and tumors. The nanoparticle compositions of the disclosure combine an immunostimulant with a photosensitizer using a nanoparticle delivery platform. For example, zinc pthalocyanine, which is a long-wavelength absorbing photosensitizer, integrated into a polymeric nanoparticle core made up of poly(D,L-lactic-co-glycolic acid)-b-poly(ethylene glycol) (PLGA-b-PEG). The outside surface of the core can be coated with metallic nanoparticles, which are then modified with CpG-ODN. Metastatic mouse breast carcinoma cells showed significant photocytotoxicity of the hybrid after irradiation with a 660 nm LASER light and this activity was remarkably better than either treatment alone. Treatment of mouse bone marrow derived dendritic cells with the photodynamic therapy-killed 4T1 cell lysate showed that the combination of photodynamic therapy with a synergistic immunostimulant in a single nanoparticle system resulted in an immune response suitable for the treatment of such as a metastatic cancer.
    • 提供一种治疗技术,将光动力疗法的光毒性和免疫刺激能力与免疫系统的广泛功效结合起来,以降低癌细胞和肿瘤的生存能力。 本公开的纳米颗粒组合物使用纳米颗粒递送平台将免疫刺激剂与光敏剂组合。 例如,作为长波长吸收光敏剂的锌酞菁聚合在由聚(D,L-乳酸 - 共 - 乙醇酸)-b-聚(乙二醇)(PLGA-b- PEG)。 芯的外表面可以涂覆金属纳米粒子,然后用CpG-ODN进行修饰。 转移性小鼠乳腺癌细胞在用660nm激光照射后显示杂合物的显着的光细胞毒性,并且该活性明显优于单独的任一种治疗。 用光动力治疗杀死的4T1细胞裂解物处理小鼠骨髓来源的树突状细胞显示,在单个纳米颗粒系统中光动力学治疗与协同免疫刺激剂的组合导致适合于治疗诸如转移性癌症的免疫应答。