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Non-ligand polypeptide and liposome complexes as intracellular delivery vehicles

机译:非配体多肽和脂质体复合物作为细胞内递送载体

摘要

The present invention discloses compositions and methods of using intracellular delivery vehicles for delivery and transfection of DNA, RNA, polypeptides, genes, proteins, drugs and biologically active agents into cells in vitro and in vivo. The vehicle comprises a mixture of a liposome and a polypeptide lacking specificity for cellular receptors. In another embodiment, a method for intracellular delivery of biologically active agents comprising combining a non-receptor-binding protein and a liposome, incubating the mixture for a period of time, adding the biologically active agent, incubating again, and finally, introducing the resulting mixture to the cell. Preferably, the liposome is a cationic liposome. The charge ratio of cationic liposome to DNA can effectively be varied from 2:1 to 1:2. Preferably, the non-receptor-binding protein is the serum albumin of the animal source of the cell to be transfected. This inention is an improvement over, and offers several advantages compared to, previously disclosed cationic liposomal delivery vehicles which utilize receptor ligands.
机译:本发明公开了使用细胞内递送载体在体外和体内将DNA,RNA,多肽,基因,蛋白质,药物和生物活性剂递送和转染到细胞中的组合物和方法。赋形剂包含脂质体和对细胞受体缺乏特异性的多肽的混合物。在另一个实施方案中,一种用于生物活性剂的细胞内递送的方法,包括将非受体结合蛋白和脂质体结合,温育混合物一段时间,加入生物活性剂,再次温育,最后引入所得的混合到细胞中。优选地,脂质体是阳离子脂质体。阳离子脂质体与DNA的电荷比可以有效地在2:1至1:2之间变化。优选地,非受体结合蛋白是待转染细胞的动物来源的血清白蛋白。与先前公开的利用受体配体的阳离子脂质体递送载体相比,该概念是一种改进,并提供了几个优点。

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