Nanoformulation of musk-derived bioactive ingredients for nanocosmetic applications

    公开(公告)号:US09700042B2

    公开(公告)日:2017-07-11

    申请号:US14614849

    申请日:2015-02-05

    CPC classification number: A01N25/28 A01N35/04 A01N63/02

    Abstract: The composition of the Nano carrier or Nano polymers composed of Hyaluronic Acid (15-25%) and fatty acids (50-70%) cross linked with ultra-Low molecular weight chitosan (15-25%) encapsulating isolated compounds from musk and their combinations for cosmetic use as anti-aging, anti-microbial, and fragrance. Additionally, these nano-encapsulated Musk bioactive compounds (MBC) at 0.1-10% (w/w MBC/Nano polymers) could be used in textile manufacturing (carpet/rugs and clothes) to provide anti-microbial and fragrance properties. Furthermore, Musk derived products are chemically conjugated to HA polymer, FA polymer, CH polymer, HA-CH co-polymer, FA-CH co-polymer or HA-CH-FA co-polymer to be incorporated into the fabric of the textile products (carpet/rugs or clothes).

    NANOFORMULATION AND METHODS OF USE OF THYROID RECEPTOR BETA1 AGONISTS FOR LIVER TARGETING
    5.
    发明申请
    NANOFORMULATION AND METHODS OF USE OF THYROID RECEPTOR BETA1 AGONISTS FOR LIVER TARGETING 审中-公开
    用于肝脏靶向的THYROID受体BETA激活剂的使用和方法

    公开(公告)号:US20140017329A1

    公开(公告)日:2014-01-16

    申请号:US13938308

    申请日:2013-07-10

    Inventor: Shaker A. Mousa

    Abstract: A composition and an associated method for hepatic targeted delivery of thyroid receptor beta1 (TRβ1) agonist to a liver of a subject. The composition includes hydrophobic nanoparticles, a liver targeting moiety exterior to each nanoparticle and covalently bonded to each nanoparticle, and at least one TRβ1 agonist encapsulated within each nanoparticle. The nanoparticles include chitosan hybrid nanoparticles, amine-modified PLGA nanoparticles, solid lipid nanoparticles, and combinations thereof. The liver targeting moiety includes Glycyrrhetinic acid (GA), Lactobionic acid (LA), or combinations thereof.

    Abstract translation: 用于肝脏靶向递送甲状腺受体β1(TRbeta1)激动剂到受试者肝脏的组合物和相关方法。 组合物包括疏水性纳米颗粒,每个纳米颗粒外部的共价键合到每个纳米颗粒上的肝靶向部分,以及封装在每个纳米颗粒内的至少一种TRβ1激动剂。 纳米颗粒包括壳聚糖杂化纳米颗粒,胺改性的PLGA纳米颗粒,固体脂质纳米颗粒及其组合。 肝靶向部分包括甘草次酸(GA),乳酸(LA)或其组合。

    NOVEL FORMULATIONS OF FACTOR VIIa INHIBITORS AND UTILITY
    6.
    发明申请
    NOVEL FORMULATIONS OF FACTOR VIIa INHIBITORS AND UTILITY 有权
    因子VIIa抑制剂和实用新型配方

    公开(公告)号:US20130295187A1

    公开(公告)日:2013-11-07

    申请号:US13935665

    申请日:2013-07-05

    Inventor: Shaker A. Mousa

    Abstract: A method for treating a subject, such as a human patient, having a vascular disorder. The treatment method administers a therapeutic effective amount of a nanoparticle or a chemical structure to the subject to treat the disorders. The nanoparticle includes a poly L-arginine polymer and a Factor VIIa inhibitor conjugated to, or encapsulated in, the poly L-arginine polymer. The chemical structure includes a Factor VIIa inhibitor that includes at least one nitric oxide (NO) donor. The disorder may be sickle cell disease; stimulated or pathological angiogenesis associated disorders, cancer, ocular angiogenesis-mediated disorders such as diabetic retinopathy and macular degeneration, coagulation and/or platelet activation-associated disorders, pulmonary hypertension, or combinations thereof.

    Abstract translation: 用于治疗患有血管病症的受试者例如人类患者的方法。 治疗方法向受试者施用治疗有效量的纳米颗粒或化学结构以治疗疾病。 纳米颗粒包括聚L-精氨酸聚合物和与聚L-精氨酸聚合物缀合或封装的因子VIIa抑制因子。 该化学结构包括包含至少一种一氧化氮(NO)供体的因子VIIa抑制剂。 该病可能是镰状细胞病; 刺激或病理性血管生成相关疾病,癌症,眼血管生成介导的病症如糖尿病性视网膜病变和黄斑变性,凝血和/或血小板活化相关疾病,肺动脉高压或其组合。

Patent Agency Ranking