MATRIX CARRIER COMPOSITIONS, METHODS AND USES
    1.
    发明申请
    MATRIX CARRIER COMPOSITIONS, METHODS AND USES 有权
    MATRIX载体组合物,方法和用途

    公开(公告)号:US20150245993A1

    公开(公告)日:2015-09-03

    申请号:US14715585

    申请日:2015-05-18

    IPC分类号: A61K9/00 A61K9/107

    摘要: Provided is a matrix carrier composition for use in pharmaceutical delivery system, the composition comprising an intermolecular association of at least a first solid phase comprising nanoparticles having hydrophobic surface, wherein the size of the nanoparticles is in the range of about 5-1000 nm, a second solid phase, comprising a biopolymer having hydrophilic and hydrophobic parts, and a continuous phase comprising oil associated with the first and said second solid phases.

    摘要翻译: 提供一种用于药物递送系统的基质载体组合物,该组合物包含至少包含具有疏水表面的纳米颗粒的至少第一固相的分子间缔合,其中纳米颗粒的尺寸在约5-1000nm范围内, 第二固相,包含具有亲水和疏水部分的生物聚合物,以及包含与第一和第二固相相关的油的连续相。

    PHARMACEUTICAL COMPOSITIONS FOR ORAL TREATMENT OF DIABETES
    5.
    发明申请
    PHARMACEUTICAL COMPOSITIONS FOR ORAL TREATMENT OF DIABETES 审中-公开
    用于口服糖尿病治疗的药物组合物

    公开(公告)号:US20150366946A1

    公开(公告)日:2015-12-24

    申请号:US14763016

    申请日:2014-01-29

    摘要: The present invention relates to pharmaceutical compositions for oral delivery comprising at least two bioactive proteins associated with glucose metabolism, selected from the group consisting of insulin, proinsulin and C-Peptide in a delivery vehicle adapted for oral administration that provides portal delivery of bioactive proteins. The exemplary pharmaceutical compositions comprise an oil-based matrix comprising solid particulate matter suspended therein, wherein the particulate matter comprises a polysaccharide non-covalently associated with silica particles having a hydrophobic surface, wherein the polysaccharide and silica particles are non-covalently associated with the at least two bioactive proteins. The present invention further provides therapeutic uses of said pharmaceutical compositions.

    摘要翻译: 本发明涉及用于口服递送的药物组合物,其包含至少两种与葡萄糖代谢相关的生物活性蛋白质,所述生物活性蛋白质选自胰岛素,胰岛素原和C-肽,其适于口服给药,其提供生物活性蛋白质的门静脉输送。 示例性药物组合物包含悬浮在其中的固体颗粒物质的油基基质,其中所述颗粒物质包含与具有疏水性表面的二氧化硅颗粒非共价缔合的多糖,其中所述多糖和二氧化硅颗粒与所述多糖和二氧化硅颗粒非共价结合 至少两种生物活性蛋白。 本发明还提供了所述药物组合物的治疗用途。