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用于核酸递送的脂质:合成与颗粒形成

Lipids for nucleic acid delivery: synthesis and particle formation.

作者信息

Bessodes Michel, Mignet Nathalie

机构信息

Unité de Pharmacologie Chimique et Génétique, CNRS, UMR 8151, Paris, France.

出版信息

Methods Mol Biol. 2013;948:67-84. doi: 10.1007/978-1-62703-140-0_6.

Abstract

Lipidic vesicles have been extensively studied for their capacity to condensate and deliver nucleic acids to the cells. Many different amphiphilic lipidic structures have been proposed, each of them bringing some advances in nonviral gene transfection. The ionic or neutral nature of the lipids induces tremendous differences in the behavior of the corresponding liposomes, from the complexation of nucleic acid to the delivery to the cell. An efficient delivery in vitro or in vivo also depends closely on the structure of the lipids and very often, efficient liposomes in vitro have been found useless for in vivo administration.We wish to describe in this chapter the chemical synthesis of two different lipids, one cationic and the other essentially neutral, and the formulation to obtain liposomes and DNA/liposome complexes. The different ways and tricks for the formulation of the two different structures are especially highlighted.

摘要

脂质囊泡因其凝聚和向细胞递送核酸的能力而受到广泛研究。人们提出了许多不同的两亲性脂质结构,每种结构都在非病毒基因转染方面取得了一些进展。脂质的离子或中性性质会导致相应脂质体行为的巨大差异,从核酸的络合到向细胞的递送。体外或体内的有效递送也密切依赖于脂质的结构,而且常常发现体外有效的脂质体对体内给药无效。在本章中,我们希望描述两种不同脂质的化学合成,一种是阳离子脂质,另一种基本为中性脂质,以及获得脂质体和DNA/脂质体复合物的配方。特别强调了制备这两种不同结构的不同方法和技巧。

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