Liposomal nanoparticles based on steroids and isoprenoids for nonviral gene delivery

被引:10
|
作者
Maiti, Bappa [1 ]
Bhattacharya, Santanu [1 ,2 ,3 ]
机构
[1] Indian Assoc Cultivat Sci, Tech Res Ctr, Kolkata, India
[2] Indian Assoc Cultivat Sci, Sch Appl & Interdisciplinary Sci, Kolkata, India
[3] Indian Inst Sci, Dept Organ Chem, Bangalore, Karnataka, India
关键词
gene delivery; liposomal nanoparticle; ANGLE NEUTRON-SCATTERING; CATIONIC LIPIDS; IN-VITRO; TRANSFECTION EFFICIENCY; VITAMIN-E; GEMINI SURFACTANTS; DRUG-DELIVERY; VESICLE FORMATION; HIGHLY EFFICIENT; CHOLESTERYL SKELETON;
D O I
10.1002/wnan.1759
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Natural lipid molecules are an essential part of life as they constitute the membrane of cells and organelle. In most of these cases, the hydrophobicity of natural lipids is contributed by alkyl chains. Although natural lipids with a nonfatty acid hydrophobic backbone are quite rare, steroids and isoprenoids have been strong candidates as part of a lipid. Over the years, these natural molecules (steroid and isoprenoids) have been used to make either lipid-based nanoparticle or functionalize in such a way that it could form nano assembly alone for therapeutic delivery. Here we mainly focus on the synthetic functionalized version of these natural molecules which forms cationic liposomal nanoparticles (LipoNPs). These cationic LipoNPs were further used to deliver various negatively charged genetic materials in the form of pDNA, siRNA, mRNA (nucleic acids), and so on. This article is categorized under: Biology-Inspired Nanomaterials > Lipid-Based Structures
引用
收藏
页数:47
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