Reduction in vivo of the inappropriate levels of endogenous and
environmental-derived compounds by sustained-release inhibitors of .beta.-
g
    1.
    发明授权
    Reduction in vivo of the inappropriate levels of endogenous and environmental-derived compounds by sustained-release inhibitors of .beta.- g 失效
    通过β-葡萄糖醛酸酶的缓释抑制剂减少内源和环境衍生化合物的不适当水平的体内

    公开(公告)号:US4845123A

    公开(公告)日:1989-07-04

    申请号:US762339

    申请日:1985-08-05

    IPC分类号: A61K31/19 A61K31/365

    CPC分类号: A61K31/19 A61K31/365

    摘要: A method for the reduction in vivo of the inappropriate levels of endogenous and environmental-derived compounds by inhibiting the activity of .beta.-glucuronidase in a mammal which comprises the administration to the mammal of an effective amount of a water insoluble, or sparingly soluble, sustained release precursor of glucarolactone or its analog is disclosed. The sustained release precursor of glucarolactone compound is selected from the group consisting of D-glucaric acid, D-galactaric acid, and L-idaric acid or derivatives or analogs. An orally administrable preparation of the sustained release precursor of glucarolactone compound is provided in the form of a capsule tablet, such that the glucarolactone or its analog is slowly released in the stomach of the treated animal or human.

    摘要翻译: 一种通过抑制哺乳动物中β-葡糖醛酸糖苷酶的活性来减少内源和环境衍生化合物的不适当水平的方法,其包括向哺乳动物施用有效量的不溶于水的或微溶的持续的 公开了葡萄糖内酯或其类似物的释放前体。 葡萄糖内酯化合物的持续释放前体选自D-葡糖二酸,D-半乳糖酸,L-赖氨酸或其衍生物或类似物。 提供了可口服给药的葡萄糖内酯化合物的缓释前体,其形式为胶囊片剂,使得葡萄内酯酮或其类似物在经处理的动物或人的胃中缓慢释放。

    Method and composition for achieving anticarcinogenic activity
    3.
    发明授权
    Method and composition for achieving anticarcinogenic activity 失效
    用于实现抗癌活性的方法和组合物

    公开(公告)号:US5010107A

    公开(公告)日:1991-04-23

    申请号:US435543

    申请日:1989-11-13

    IPC分类号: A61K31/19

    CPC分类号: A61K31/19

    摘要: The present invention describes a protocol for achieving a very high degree of anticarcinogenic (or chemopreventive or cancer preventative) activity through the combination of a low suboptimal dose of a D-glucarolactone-based dietary anticarcinogen (i.e., calcium glucarate or CGT) with a low suboptimal dose of retinoid-based anticarcinogen (4-hydroxyphenyl retinamide or HPR). Since synergism is obtained by this combination, these two anticarcinogens can be employed at dosages far below toxic levels and at dosages that are practical as a food supplement.

    摘要翻译: 本发明描述了通过将低次最低剂量的基于D-葡萄糖内酯的饮食抗癌药(即,葡萄糖酸钙或CGT)与低浓度的低葡萄糖酸(例如葡萄糖酸钙或CGT)的组合来实现非常高程度的致癌(或化学预防或癌症预防)活性的方案 次要剂量的类视黄醇类抗癌药(4-羟基苯基视黄酰胺或HPR)。 由于通过这种组合获得了协同作用,所以这两种抗癌剂可以以低于毒性水平的剂量和作为食品补充剂实用的剂量使用。

    Method and composition for achieving cancer chemopreventive and
chemotherapeutic activity
    4.
    发明授权
    Method and composition for achieving cancer chemopreventive and chemotherapeutic activity 失效
    用于实现癌症化学预防和化学治疗活性的方法和组合物

    公开(公告)号:US4997852A

    公开(公告)日:1991-03-05

    申请号:US436049

    申请日:1989-11-13

    IPC分类号: A61K31/19

    CPC分类号: A61K31/19

    摘要: The present invention describes a protocol for achieving a very high degree of anticarcinogenic (chemopreventive and chemotherapeutic) activity through the combination of low suboptimal doses of a D-glucarolactone-based dietary anticarcinogen with low suboptimal doses of a retinoid-based anticarcinogen. Synergism is obtained by this combination and these two anticarcinogens can be employed at dosages far below toxic levels and at dosages that are practical as a food supplement.

    摘要翻译: 本发明描述了通过低次要剂量的基于D-葡萄糖内酯的膳食抗癌药与低次优剂量的基于类视黄醇的抗癌药物的组合来实现非常高程度的致癌(化学预防和化学治疗)活性的方案。 通过这种组合获得协同作用,并且这两种抗癌剂可以以低于毒性水平的剂量和作为食物补充剂实用的剂量使用。

    Method and composition for achieving chemotherapeutic activity
    5.
    发明授权
    Method and composition for achieving chemotherapeutic activity 失效
    达到化疗活性的方法和组成

    公开(公告)号:US5008291A

    公开(公告)日:1991-04-16

    申请号:US436046

    申请日:1989-11-13

    IPC分类号: A61K31/19

    CPC分类号: A61K31/19

    摘要: The present invention describes a dietary supplement for achieving a very high degree of chemotherapeutic activity through the synergistic combination of a low suboptimal dose of a D-glucarolactone-based dietary anticarcinogen (calcium glucarate) with a low suboptimal dose of retinoid-based anticarcinogen (4-hydroxyphenyl retinamide).

    摘要翻译: 本发明描述了通过低次优剂量的基于D-葡萄糖内酯的饮食抗癌药(葡糖二酸钙)与低次要剂量的基于类视黄醇的抗癌药(4)的协同组合来实现非常高程度的化疗活性的膳食补充剂 - 羟基苯基视黄酰胺)。

    Detection of circulating antibodies to a cancer marker protein
    6.
    发明授权
    Detection of circulating antibodies to a cancer marker protein 失效
    检测癌症标记蛋白的循环抗体

    公开(公告)号:US4937185A

    公开(公告)日:1990-06-26

    申请号:US79870

    申请日:1987-07-31

    摘要: A method and kit are described for detecting the presence of cancers and pre-neoplastic cells that produce an oncofetal phosphoprotein having a molecular weight of approximately 60,000 and having the capacity to increase the release of ribonucleic acid from cell nuclei. The method involves detecting the presence of auto-antibodies to this oncofetal phosphoprotein in a subject suspected of suffering from a cancer or pre-neoplastic cells which produce this cancer marker protein. The kit includes purified oncofetal phosphoprotein.

    摘要翻译: 描述了一种方法和试剂盒,用于检测产生分子量约为60,000并具有增加核糖核酸从细胞核中释放的能力的癌症和前赘生物细胞的存在。 该方法涉及检测疑似患有癌症或产生该癌症标志物蛋白质的前赘生物细胞的受试者中该蛋白质磷蛋白的自身抗体的存在。 该试剂盒包括纯化的蛋白质磷蛋白。

    Method for treating cancer with monoclonal antibodies to oncofetal
protein
    7.
    发明授权
    Method for treating cancer with monoclonal antibodies to oncofetal protein 失效
    用单克隆抗体对癌胚蛋白治疗癌症的方法

    公开(公告)号:US5688505A

    公开(公告)日:1997-11-18

    申请号:US449336

    申请日:1995-05-24

    摘要: The present invention provides a low cost, less toxic, anti-cancer immunotherapy which enhances the host's immune system ability to destroy or contain cancers, and also provides a diagnostic test for cancer. Specifically, the present invention provides monoclonal antibodies specific for, that is, specifically bind, oncofetal protein (OFP), a cancer cell product. Tumors treated with a single dose of the monoclonal antibodies against OFP are markedly reduced in size, and leukemic populations of cells treated with a single does of monoclonal antibodies against OFP are significantly decreased in number. Since the monoclonal antibodies of the present invention do not bind to tumor cells, the monoclonal antibody treatment overcomes the disadvantages associated with tumor cell targeting. Monoclonal antibodies to OFP offer a simple and inexpensive agent for use as a primary or adjuvant therapy against a wide variety of cancers and tumors in humans and other animals. The monoclonal antibodies against OFP are also employed to detect cancer in animal, including human patients.

    摘要翻译: 本发明提供了低成本,毒性较小的抗癌免疫疗法,其增强了宿主的免疫系统破坏或容纳癌症的能力,并且还提供了癌症的诊断试验。 具体地说,本发明提供了特异性,特异性结合成骨蛋白(OFP),癌细胞产物的单克隆抗体。 用单剂量的针对OFP的单克隆抗体治疗的肿瘤的大小显着降低,并且使用单一针对OFP的单克隆抗体处理的细胞的白血病群体的数量显着减少。 由于本发明的单克隆抗体不与肿瘤细胞结合,所以单克隆抗体治疗克服了与肿瘤细胞靶向相关的缺点。 OFP的单克隆抗体提供了一种简单而廉价的药物,可用作针对人类和其他动物中各种癌症和肿瘤的主要或辅助治疗。 针对OFP的单克隆抗体也用于检测动物,包括人类患者中的癌症。

    Method of producing monoclonal antibodies to oncofetal protein
    8.
    发明授权
    Method of producing monoclonal antibodies to oncofetal protein 失效
    生产蛋白质单克隆抗体的方法

    公开(公告)号:US5650300A

    公开(公告)日:1997-07-22

    申请号:US452252

    申请日:1995-05-26

    摘要: The present invention provides a low cost, less toxic, anti-cancer immunotherapy which enhances the host's immune system ability to destroy or contain cancers, and also provides a diagnostic test for cancer. Specifically, the present invention provides monoclonal antibodies specific for, that is, specifically bind, oncofetal protein (OFP), a cancer cell product. Tumors treated with a single dose of the monoclonal antibodies against OFP are markedly reduced in size, and leukemic populations of cells treated with a single does of monoclonal antibodies against OFP are significantly decreased in number. Since the monoclonal antibodies of the present invention do not bind to tumor cells, the monoclonal antibody treatment overcomes the disadvantages associated with tumor cell targeting. Monoclonal antibodies to OFP offer a simple and inexpensive agent for use as a primary or adjuvant therapy against a wide variety of cancers and tumors in humans and other animals. The monoclonal antibodies against OFP are also employed to detect cancer in animal, including human patients.

    摘要翻译: 本发明提供了低成本,毒性较小的抗癌免疫疗法,其增强了宿主的免疫系统破坏或容纳癌症的能力,并且还提供了癌症的诊断试验。 具体地说,本发明提供了特异性,特异性结合成骨蛋白(OFP),癌细胞产物的单克隆抗体。 用单剂量的针对OFP的单克隆抗体治疗的肿瘤的大小显着降低,并且使用单一针对OFP的单克隆抗体处理的细胞的白血病群体的数量显着减少。 由于本发明的单克隆抗体不与肿瘤细胞结合,所以单克隆抗体治疗克服了与肿瘤细胞靶向相关的缺点。 OFP的单克隆抗体提供了一种简单而廉价的药物,可用作针对人类和其他动物中各种癌症和肿瘤的主要或辅助治疗。 针对OFP的单克隆抗体也用于检测动物,包括人类患者中的癌症。

    Monoclonal antibody to canine placental oncofetal protein for detecting
cancer
    9.
    发明授权
    Monoclonal antibody to canine placental oncofetal protein for detecting cancer 失效
    犬胎盘蛋白单克隆抗体用于检测癌症

    公开(公告)号:US5532159A

    公开(公告)日:1996-07-02

    申请号:US222201

    申请日:1994-04-01

    摘要: The present invention provides a low cost, less toxic, anti-cancer immunotherapy which enhances the host's immune system ability to destroy or contain cancers, and also provides a diagnostic test for cancer. Specifically, the present invention provides monoclonal antibodies specific for, that is, specifically bind, oncofetal protein (OFP), a cancer cell product. Tumors treated with a single dose of the monoclonal antibodies against OFP are markedly reduced in size, and leukemic populations of cells treated with a single does of monoclonal antibodies against OFP are significantly decreased in number. Since the monoclonal antibodies of the present invention do not bind to tumor cells, the monoclonal antibody treatment overcomes the disadvantages associated with tumor cell targeting. Monoclonal antibodies to OFP offer a simple and inexpensive agent for use as a primary or adjuvant therapy against a wide variety of cancers and tumors in humans and other animals. The monoclonal antibodies against OFP are also employed to detect cancer in animal, including human patients.

    摘要翻译: 本发明提供了低成本,毒性较小的抗癌免疫疗法,其增强了宿主的免疫系统破坏或容纳癌症的能力,并且还提供了癌症的诊断试验。 具体地说,本发明提供了特异性,特异性结合成骨蛋白(OFP),癌细胞产物的单克隆抗体。 用单剂量的针对OFP的单克隆抗体治疗的肿瘤的大小显着降低,并且使用单一针对OFP的单克隆抗体处理的细胞的白血病群体的数量显着减少。 由于本发明的单克隆抗体不与肿瘤细胞结合,所以单克隆抗体治疗克服了与肿瘤细胞靶向相关的缺点。 OFP的单克隆抗体提供了一种简单而廉价的药物,可用作针对人类和其他动物中各种癌症和肿瘤的主要或辅助治疗。 针对OFP的单克隆抗体也用于检测动物,包括人类患者中的癌症。