miRNA Delivery by Nanosystems: State of the Art and Perspectives

被引:47
作者
Moraes, Fernanda C. [1 ]
Pichon, Chantal [2 ]
Letourneur, Didier [1 ]
Chaubet, Frederic [1 ]
机构
[1] Univ Paris, Univ Sorbonne Paris Nord, LVTS, INSERM U1148, F-75018 Paris, France
[2] Univ Orleans, Ctr Biophys Mol, CNRS, UPR4301, F-45071 Orleans, France
关键词
miRNA delivery; non-viral vectors; nanoparticles; NEGATIVE BREAST-CANCER; NANOPARTICLE-MEDIATED DELIVERY; SOLID LIPID NANOPARTICLES; CO-DELIVERY; MICRORNA DELIVERY; SIRNA DELIVERY; IN-VITRO; CHITOSAN NANOPARTICLES; TARGETED DELIVERY; PLASMID DNA;
D O I
10.3390/pharmaceutics13111901
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNAs (miRNAs) are short (~21-23 nucleotides), non-coding endogenous RNA molecules that modulate gene expression at the post-transcriptional level via the endogenous RNA interference machinery of the cell. They have emerged as potential biopharmaceuticals candidates for the treatment of various diseases, including cancer, cardiovascular and metabolic diseases. However, in order to advance miRNAs therapeutics into clinical settings, their delivery remains a major challenge. Different types of vectors have been investigated to allow the delivery of miRNA in the diseased tissue. In particular, non-viral delivery systems have shown important advantages such as versatility, low cost, easy fabrication and low immunogenicity. Here, we present a general overview of the main types of non-viral vectors developed for miRNA delivery, with their advantages, limitations and future perspectives.
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页数:20
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