首页> 外国专利> NANOPARTICLE COMPOSITE SHOWING IMPROVED ENDOCYTOSIS EFFICIENCY THROUGH SURFACE MODIFICATION USING LIPID AND MANUFACTURING METHOD THEREFOR

NANOPARTICLE COMPOSITE SHOWING IMPROVED ENDOCYTOSIS EFFICIENCY THROUGH SURFACE MODIFICATION USING LIPID AND MANUFACTURING METHOD THEREFOR

机译:纳米粒子复合材料显示通过使用脂质和制造方法的表面改性改善的内吞作用效率

摘要

The present disclosure relates to a nanoparticle complex that is taken into cells to be used for the treatment of diseases, and a method of manufacturing the same. More particularly, the present disclosure relates to a nanoparticle complex and a method of manufacturing the same using a top-down process. In the top-down process, surfaces of nanoparticles are modified with a lipid-based material having high stability and excellent biocompatibility, thereby improving cellular uptake. A lipid structure having a tube shape is bonded to a portion of the surface of the nanoparticle so that the nanoparticle complex undergoes endocytosis, directly penetrates a cell membrane, and is effectively taken into spheroid-type tumor cells. The lipid structure is not directly attached to the nanoparticle, lipid-based lipidomes (such as bubbles and liposomes) are bonded to the nanoparticles, and mechanical force is applied thereto to thus crush the lipidomes, so that the lipid structure is formed on the surface of the nanoparticles. Since a top-down process is used, it is possible to easily mass-produce the nanoparticle complex.
机译:本公开涉及一种纳米颗粒复合物,其被纳入用于治疗疾病的细胞,以及制造方法的方法。更具体地,本公开涉及一种纳米颗粒复合物和使用自水下处理的制造方法。在自上而下的过程中,用具有高稳定性和优异生物相容性的脂质的材料改性纳米颗粒表面,从而改善细胞摄取。具有管形状的脂质结构粘合到纳米颗粒的一部分中,使得纳米颗粒复合物经历内吞作用,直接穿透细胞膜,并有效地将球膜造成肿瘤细胞。脂质结构未直接连接到纳米颗粒上,脂质基脂质体(例如气泡和脂质体)与纳米颗粒键合,并施加机械力以使其压碎脂质体,从而在表面上形成脂质结构纳米颗粒。由于使用了自上而下的方法,可以容易地批量生产纳米颗粒复合物。

著录项

  • 公开/公告号EP3808344A1

    专利类型

  • 公开/公告日2021-04-21

    原文格式PDF

  • 申请/专利权人 SOGANG UNIVERSITY RESEARCH FOUNDATION;

    申请/专利号EP20180920326

  • 发明设计人 KIM HYUN CHEOL;KIM DO YEON;

    申请日2018-09-04

  • 分类号A61K9/50;A61K9/51;A61K9/127;A61K47/69;A61K45/06;

  • 国家 EP

  • 入库时间 2022-08-24 18:18:40

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