NANO-TARGETED DELIVERY OF PROTEASE, POLYMERASE INHIBITORS WITH OR WITHOUT IMMUNE MODULATORS IN THE TREATMENT OF HEPATITIS C
    34.
    发明申请
    NANO-TARGETED DELIVERY OF PROTEASE, POLYMERASE INHIBITORS WITH OR WITHOUT IMMUNE MODULATORS IN THE TREATMENT OF HEPATITIS C 审中-公开
    蛋白酶,聚合酶抑制剂与免疫调节剂在治疗乙型肝炎方面的NANO定向交付

    公开(公告)号:US20150224134A1

    公开(公告)日:2015-08-13

    申请号:US14614496

    申请日:2015-02-05

    Inventor: Shaker A. Mousa

    Abstract: This disclosure concerns novel formulation and Nanoformulations as defined in the specification and compositions comprising combination of HCV protease and polymerase inhibitors, with or without interferon, along with anti-fibrotic/anti-hemolytic agents' combination of naturally driven Polyphenol/Thiols, and Non-anticoagulant GAGs. These compounds are effective antiviral agents, especially in inhibiting the function of the various genotypes of Hepatitis C virus (HCV). Thus, the disclosure also concerns a method of treating HCV related diseases or conditions by use of these novel compounds or a composition comprising nano-targeted delivery of novel nanoformulation containing combined composition for HCV and/or hepatic targeted delivery for improved efficacy and safety.

    Abstract translation: 本公开涉及如本说明书中定义的新型制剂和纳米制剂,其包含具有或不具有干扰素的HCV蛋白酶和聚合酶抑制剂的组合以及天然驱动的多酚/硫醇与抗纤维化/抗溶血剂的组合的组合, 抗凝剂GAGs。 这些化合物是有效的抗病毒剂,特别是抑制丙型肝炎病毒(HCV)各种基因型的功能。 因此,本公开还涉及通过使用这些新化合物或包含纳米靶向递送含有用于HCV和/或肝靶向递送的组合组合物的新型纳米制剂的组合物来治疗HCV相关疾病或病症的方法,以提高功效和安全性。

    COMPOSITION AND METHOD FOR SULFATED NON-ANTICOAGULANT LOW MOLECULAR WEIGHT HEPARINS IN CANCER AND TUMOR METASTASIS
    35.
    发明申请
    COMPOSITION AND METHOD FOR SULFATED NON-ANTICOAGULANT LOW MOLECULAR WEIGHT HEPARINS IN CANCER AND TUMOR METASTASIS 审中-公开
    癌症和肿瘤组织中非抗血清低分子重量蛋白的组合物和方法

    公开(公告)号:US20150132399A1

    公开(公告)日:2015-05-14

    申请号:US14526660

    申请日:2014-10-29

    Inventor: Shaker A. Mousa

    Abstract: A nanoformulation that includes nanoparticles. Each nanoparticle includes a shell in which a glycosaminoglycan (GAG is encapsulated. The GAG is ionically or covalently bonded to the shell. The GAG is selected from the group consisting of sulfated non-anticoagulant heparin (SNACH), super-sulfated non-anticoagulant heparin (S-SNACH), and a combination thereof. The shell includes Poly (lactic-co-glycolic acid) (PLGA), Polyethylene Glycol (PEG)-PLGA, maleimide-PEG-PLGA, chitosan, chitosan-PLGA, methoxy-polyethyleneglycol-poly (lactide-co-glycolide) (MPEG-PLGA)-(maleimide-PEG-PLGA), PLGA-Polycaprolate, or calcium alginate. A method of using the nanoformulation to treat a cancer in a subject includes administering to the patient a therapeutically effective amount of the nanoformulation for treating the cancer.

    Abstract translation: 包括纳米颗粒的纳米制剂。 每个纳米颗粒包括壳聚糖,其中糖胺聚糖(GAG被封装),GAG离子或共价键合到壳上,GAG选自硫酸化非抗凝血剂肝素(SNACH),超硫酸化非抗凝血剂肝素 (S-SNACH)及其组合,壳包括聚(乳酸 - 共 - 乙醇酸)(PLGA),聚乙二醇(PEG)-PLGA,马来酰亚胺-PEG-PLGA,壳聚糖,壳聚糖-PLGA,甲氧基 - 聚乙二醇 - 聚(丙交酯 - 共 - 乙交酯)(MPEG-PLGA) - (马来酰亚胺-PEG-PLGA),PLGA-聚己内酯或藻酸钙。使用纳米制剂治疗受试者的癌症的方法包括向患者施用 治疗有效量的用于治疗癌症的纳米制剂。

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