Formulation approaches to short interfering RNA and MicroRNA: Challenges and implications

被引:59
作者
Guzman-Villanueva, Diana [1 ,2 ]
El-Sherbiny, Ibrahim M. [1 ,3 ,4 ]
Herrera-Ruiz, Dea [2 ]
Vlassov, Alexander V. [5 ]
Smyth, Hugh D. C. [1 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
[2] Univ Autonoma Estado Morelos, Fac Farm, Cuernavaca 62209, Morelos, Mexico
[3] Zewail City Sci & Technol, October City 6, Giza, Egypt
[4] Mansoura Univ, Fac Sci, Chem Dept, ET-35516 Mansoura, Egypt
[5] Life Technol, Austin, TX 78744 USA
关键词
siRNA; miRNA; RNA interference; RNAi; in vivo knockdown; formulations; polymers; lipid; nonviral gene delivery; oligonucleotides; viral vectors; GENE DELIVERY-SYSTEM; IN-VIVO DELIVERY; IMPROVING SIRNA DELIVERY; TRANSFECTION EFFICIENCY; TARGETED DELIVERY; CHEMICAL-MODIFICATION; NONVIRAL VECTORS; CATIONIC LIPIDS; CHITOSAN; THERAPY;
D O I
10.1002/jps.23300
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
RNA interference has emerged as a potentially powerful tool in the treatment of genetic and acquired diseases by delivering short interfering RNA (siRNA) or microRNA (miRNA) to target genes, resulting in their silencing. However, many physicochemical and biological barriers have to be overcome to obtain efficient in vivo delivery of siRNA and miRNA molecules to the organ/tissue of interest, thereby enabling their effective clinical therapy. This review discusses the challenges associated with the use of siRNA and miRNA and describes the nonviral delivery strategies used in overcoming these barriers. More specifically, emphasis has been placed on those technologies that have progressed to clinical trials for both local and systemic siRNA and miRNA delivery. (C) 2012 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:40464066, 2012
引用
收藏
页码:4046 / 4066
页数:21
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